Fordham University            The Jesuit University of New York

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Mentored Research and Other Projects of Current RETI Fellows

Cohort 1 Fellows (2011-2013)

Cohort 2 Fellows (2012-2014)

Cohort 3 Fellows (2013-2015)

Cohort 1 Fellows

Michelle Broaddus, Ph.D.

Participant perspectives of risks and benefits of participating in a text message-delivered intervention for safer sex communication

Abstract: Text-messaging may offer a new effective medium of HIV prevention intervention delivery. The lack of established precedents to these innovative modalities means new ethical concerns should be considered. Privacy of participants and security of data may be of most importance to IRBs. However, denying access to these interventions may undermine principles of beneficence, and respect for persons, and may not reflect participants’ views of the potential interventions’ benefits versus risks. Aim: To survey potential participants’ perceptions of risks and benefits of participating in a sexual communication intervention delivered via text messaging compared to face-to-face. Participants: Young African American women recruited from an STI clinic. Method: Three focus groups, 100 surveys (to be collected). Results/Conclusion: Focus groups results indicate high levels comfort with a text message-based intervention, identified barriers and benefits to both modalities, and suggested ways to increase benefit of text message based intervention.

Selected recent publications and presentations:
Broaddus, M. R., & Dickson-Gomez, J. (2013). Text Messaging for Sexual Communication and Safety Among African American Young Adults. Qualitative health research, 23(10), 1344-1353.

Broaddus, M., Marsch, L. (2013, March). Young African-American women’s perceptions of the risks and benefits of participating in a text message-delivered sexual communication intervention. Paper presented at the national conference of the Society for Behavioral Medicine, San Francisco, CA.

Broaddus, M., DiFranceisco, W., Kelly, J., St. Lawrence, J., Amirkhanian, Y., Pearson, B., & Vann-Beets, P. (2013, March). Social media use and sexual risk behavior among Black MSM in three cities. Poster presented at the national conference of the Society for Behavioral Medicine, San Francisco, CA.

Broaddus, M. (2013). Participant Perspectives of Risks and Benefits of Participating in a Text-Message-delivered Intervention for Safer Sex Communication. JERHRE Special Issue (In Press). 

Peter Davidson, Ph.D.

Disjuncts in understanding: An exploration of differences in the ways drug users, researchers, and federal code understand research participation

Abstract: The research will utilize a grounded theory / situational analysis approach to explore how a specific population of young people who inject drugs understand and experience participation in epidemiologic research, and will compare these understandings with those embedded in US Federal Code regulating research with human subjects, as well as with perspectives provided by researchers and IRB members. The research is expected to offer insight into disjuncts in understanding which have the potential to inadvertently leave research participants feeling mistreated.
Selected recent publications and presentations:
Davidson, P., & Page, K. (2012). Research participation as work: comparing the perspectives of researchers and economically marginalized populations.American journal of public health, 102(7), 1254-1259.

Davidson, PJ. (2012). Differences between the ways researchers and people who inject drugs think about research participation, and the ethical consequences of these differences. National Harm Reduction Conference, November 2012, Portland Oregon.

Jennifer Hettema, Ph.D.

Physician attitudes and behavior towards HIV+ IDUs

Abstract: While adherence to HAART may be affected among IDUs, due to the instable lifestyle associated with drug seeking and use (Wood et al., 2008), the risk of development of antiretroviral resistance among IDUs has not been found to be higher than their non-IDU counterparts (Werb et al., 2010). Despite this, IDU status has been found effect access to care for HIV (WHO, 2006; Wood et al., 2008), with evidence that physician reluctance to prescribe HIV may play contribute to this disparity (Bassetti, 1999; Ding et al., 2005). To determine the impact of IDU status on physician prescribing behavior, a national sample of community-based HIV prescribing providers completed an online survey in which they were presented with two case vignettes describing a patient with previous adherence issues presenting for treatment and requesting reinstatement on antiretroviral medications. The vignettes were identical with the exception of the IDU status of the patient. Participants were randomly assigned to see either the IDU or non-IDU (NIDU) vignette first. To date 156 participants have consented to participate in the study and 112 of these submitted complete responses. Participants were predominately female (55.8%), White (77.9%), and practicing in Urban settings (80.5%). Participants were well distributed by state. Most participants were physicians (47.8%) or nurse practioners (45.1%), with a smaller samples of physician assistants (7.1%). Independent samples t-tests revealed that neither IDU prescribing behavior (t(118)=-.258, p=.797) nor NIDU prescribing behavior (t(117)=-.693) differed significantly by condition (order of presentation). Consequently, conditions were collapsed for future analyses. A paired samples t-test was conducted to evaluate the impact of patient IDU status on prescribing behavior. There was a statistically significant difference between reported likelihood of prescribing for NIDU (M=3.51, SD=1.37) versus IDU patients (M=3.03, SD=1.37), t(115) = -5.03, p < .001. Attitudes towards shared decision making and concerns about adherence are both predictive of less willingness to prescribe to IDUs.

Selected recent publications and presentations:
Hettema, J.E., Russo, J., Fisher, C., & Cockrell, S. (April, 2013) Disparities in prescribing behavior towards injection drug users living with HIV. Poster presented at the New Mexico Public Health Association Disparity to Equity Conference. Albuquerque, NM.

Hettema, J.E. (July 2013). Disparities in prescribing behavior towards injection drug users living with HIV.  Lecture given at the 2013 Fordham University HIV Prevention Research Ethics Training Institute.

Hettema, J.E., Russo, J.M., & Fisher, C.B. (August, 2013). Disparities in Prescribing Behavior Towards Injection Drug Users. Poster to be presented at the American Psychological Association Annual Convention. Honolulu, HI.

Hettema, J.E., Russo, J.M., & Fisher, C.B. (November, 2013). Disparities in prescribing behavior towards injection drug users living with HIV. Oral presentation as part of the symposium titled Enhancing the Responsible Conduct of HIV Treatment and Prevention in Community Contexts moderated by Celia Fisher. American Public Health Association Annual Meeting: Boston, MA.

Kristin Kostick, Ph.D.

Exploring participant experiences in a peer-delivered HIV intervention with IV drug users

Abstract: The goal of this project is to use qualitative methodologies to explore the role of communication between research staff and patients involved in a peer-delivered HIV risk and harm reduction program for intravenous (IV) drug users in Hartford, CT. Peer-delivered interventions among drug users have come under close scrutiny by ethics researchers because of their potential to inadvertently and negatively impact patient rehabilitation efforts due to continued exposure to and engagement with drug-using social networks in conjunction with peer-delivered intervention strategies. This study aims to explore whether enhanced communication of patient concerns and experiences with research staff may help to reduce the potential for inadvertent maleficence in peer-delivered drug treatment interventions.
Selected recent publications and presentations:
Kostick, K.  (March 2013). Denver. Participant and Staff Experiences in a Peer-Delivered HIV Intervention with Injection Drug Users. Society for Applied Anthropology Meeting.

Kostick, K. (2013). Exploring Participant Experiences in Peer-Delivered HIV Intervention with IV Drug Users. JERHRE Special Issue (In Press).

Purnima Madhivanan, M.B.B.S., M.P.H., Ph.D.

Ethical issues in the deliver of prevention of mother-to-child transmission of HIV interventions in South India

Abstract: BACKGROUND: GOI recently changed guidelines for HIV testing from “opt-out” testing to routine HIV testing of all pregnant women receiving antenatal care. PARTICIPANTS: This qualitative study examined the experiences and perceptions of recently delivered women undergoing HIV testing during ANC and healthcare workers who conduct HIV testing and counseling in government and private hospitals in Mysore, Karnataka, India. METHODS: 2 FGD carried out among recently delivered HIV-negative women who underwent HIV testing to explore women’s experiences with pre-test counseling; informed consent; and HIV testing during their antenatal care. In addition, a FGD with healthcare workers involved with HIV testing was carried out to assess KAP around HIV testing of pregnant women. RESULTS: Only six of the 15 women recalled being informed about the purpose of routine HIV testing. A large majority of the women (11) said that only their doctor informed them that they had to get an HIV test if they wished to deliver at the hospital. Only 3of the 15 women said they recalled signing a consent form for testing but a majority (8) said they had been given forms that they were told to sign. The seven HCW attending the FGD had sufficient knowledge about HIV testing and PMTCT. While they said that they kept confidentiality about women’s HIV test results, many admittedthat other hospital employees might occasionally find out about a women’s HIV status. In addition, several expressed derogatory and stigmatizing remarks about “uneducated rural women” who did not comprehend HIV counseling or understand the reasons for giving consent. CONCLUSIONS: Women are poorly informed about the risks and reasons for routine antenatal HIV testing. Healthcare workers should be further trained on confidentiality and informed consent in addition to sensitizing them about the need for non-stigmatizing HIV care and testing.

Selected recent publications and presentations:
Madhivanan, P., et al. (2012). Ethical issues in the delivery of prevention of mother-to-child transmission of HIV interventions in Mysore, South India. 4th National Bioethics Conference, December 5-8, 2012, Hyderabad, India.

Cynthia Pearson, Ph.D.
Human subject research training for community researchers: A Pacific Northwest Native American cultural prospective

Abstract: This RETI mentored research project will develop a model to adapt and augment the Collaborative Institutional Training Initiative (CITI) human subject certification training curriculum. The model will describe the steps taken to adapt a CITI module to be culturally-responsive and user friendly for rural American Indian (AI) community researchers from Pacific Northwest tribal communities. An expert panel of AI academic and community researchers will prioritize focus areas; adapt and augment components from 1 to 2 CITI Social and Behavioral Sciences modules, highlighting cultural relevance (i.e. sovereignty), priorities and values. The Aims are: 1) in collaboration with Pacific Northwest tribal partners, define the process to produce a culturally relevant CITI human subject certification curriculum module; and 2) produce and evaluate the validity of the culturally-adapted module among 40 tribal members who: a) are 18 years or older; 2) have never taken the CITI training; 3) currently collaborate with an academic research partner or are interested in research; and, 4) reside on a reservation. Improving human subject training usability and cultural relevance for community partners will enhance HIV prevention research ethics practices.

Selected recent publications and presentations: 
Pearson, C. (2013). Human Subject Research Training for HIV and Drug Use Community Researchers: A Pacific Northwest Native American Cultural Perspective. JERHRE Special Issue (In Press).

Pearson C.R, Walters K.L, Simoni J.M, Beltran, R., Nelson, K.M.  A cautionary tale: Risk reduction strategies among urban American Indian/Alaskan Native men who have sex with men. (Feb. 2013) AIDS Education and Prevention Volume 25 (1):25-37; PMID 23387949

Pearson, C.R. “Enhancing the Responsible Conduct of HIV Prevention Research across Culturally and Globally Diverse Populations” Submitted Ethics SPIG: Oral presentation APHA Conference November 2-6 2013, Boston, MA.

Pearson, C.R. & Parker, M. “Are the CITI Certification Modules Adequate to Ensure Human Subjects Protections in Community Based Participatory Research?  A Case Example from Indian Country” Oral presentation, Public Responsibility in medicine and Research PRIMR 2013, Advancing Ethical Research Conference November 7-9 Boston MA Oral presentation.

Pearson, C.R., Cassels, S., *Whitefoot, P., Symposium presentation “HIV risk and protective factors in place and space: Partnering among American Indian and Alaskan Native young adults” U.S. Conference on AIDS 2013, September 8-11, 2013, in New Orleans.

Walters, K.L., LaMarr, J., Levy, R. L., Pearson, C.R., Maresca, T., Mohammed, S.A., Simoni, J.M., Evans-Campbell, T., Fredriksen-Goldsen, K., Fryberg, S., Jobe, J.B., (2012) “Project həli?dxw: The Development and Evaluation Design of a Tribally Based Cardiovascular Disease Prevention Intervention for American Indian Families.” The Journal of Primary Prevention: Aug; 33(4):197-207. PMID: 22965622; PMC3505854

Evans-Campbell, T., Walters K., Pearson, C.R., C. Campbell, Indian Boarding School, Substance Use, And Mental Health Among Two-Spirit urban American Indian/Alaska Natives (2012). The American Journal of Drug and Alcohol Abuse. Sept 38 (5): 421-7. PMID:22931076

Rao, D., Chen, W-T., Pearson, C., Simoni, J., Fredriksen-Goldsen, K., Nelson, K., Zhao, H., Zhang, F. Social Support Mediates the Relationship between HIV Stigma and Depression/ Quality of Life among People Living with HIV in Beijing, China. (2012)  Int J STD AIDS (23) 481-484. PMID: 22844001; PMC3408622

Hicks, S., Duran, B., Wallerstein, N., Avila, M., Belone, L., Lucero, J.,  Magarati, M.,  Mainer, E., Martin, D.,  Muhammad, Oetzel, J.,  Pearson, C.,  Sahota, Simonds, V.  and Sussman, A.,  Evaluating Community-Based Participatory Research (CBPR) to Improve Community-Partnered Science and Community Health. (2012) Progress in Community Health Partnerships: Research, Education, and Action. Fall 6 (3): 289-99 PMID: 22982842

Sandoval, J., Lucero, J., Oetzel, J., Avila, M., Belone, L., Mau M., Pearson C., Tafoya G., Duran B., Iglesias Rios L., Wallerstein N.  (2012) Process and outcome constructs for evaluating community based participatory research.  Health Education Research. 27 (4), 680-690. PMID: 21940460; PMC3396879

Nelson KM, Simoni JM, Pearson CR, Walters KL. (2011) ‘‘I've had unsafe sex so many times why bother being safe now?’’: The role of cognitions in sexual risk among American Indian/Alaska Native men who have sex with men. Annals of Behavioral Medicine Dec 42(3):370-80 PMID:21887585; PMC3272360
Elizabeth Reed, M.P.H., Sc.D.
Perceptions of HIV prevention research participation among women working as sex workers in Andhra Pradesh, India

Abstract: The proposed project aims to explore qualitatively the perspectives of female sex workers (FSW) in Rajahmundry, Andhra Pradesh (India) regarding their participation in HIV research studies, with primary focus on ethical issues in research. FSW face multiple burdens due to various contextual challenges in their lives, as well as high levels of stigma and related discrimination. Thus, efforts are needed toensure that research is being conducted in a way that is most ethical, and specifically considers the multitude of unique factors relevant to women working as sex workers in this high HIV prevalence region of India. Findings will inform the implementation of future HIV prevention research efforts in this context, determine whether revisions to research ethics protocols are needed as well as to guide such changes, and have implications for work conducted in similar settings.

Selected recent publications and presentations:

Reed, E. (2013). Perceptions of HIV Prevention Research Participation Among Women Working as Sex Workers in Andhra Pradesh, India. JERHRE Special Issue (In Press).

Reed, E. (2013). Confidentiality, Privacy, & Respect: Perspectives of Female Sex Workers Participating in HIV Prevention Research in Andhra Pradesh, India, APHA, Boston, MA.

Reed, E. (2012). Perceptions of HIV Prevention Research Participation among Women Working as Sex Workers in Andhra Pradesh, India; International Conference on AIDS, Washington, DC.

Lianne Urada, Ph.D., M.S.W., L.C.S.W.
Social and structural constraints on disclosure and informed consent with female sex workers and their managers in the Philippines

Abstract: Aim: This project explored the experiences of female sex workers (FSWs) working in night clubs, karaoke bars, and spa/saunas in the Philippines in participating in behavioral HIV prevention research, including their process of consent to research, their knowledge of research ethics, barriers to disclosure of sensitive topics, and the necessary conditions for their involvement in HIV research prevention interventions. Participants: 7 former interviewers participated in a focus group, and 20 FSWs and 10 establishment managers were interviewed individually as key informants about the research process. Method: This qualitative research used semi-structured interview guides for the individual interviews, focus group, and community advisory board meetings, and ethnographic approaches. Results: Emergent themes include FSW issues with trust of the research and interviewer, intrusiveness of survey questions, problems seeing any changes made as a result of the research, and feeling forced by government to do surveys. FSWs expressed desire to actively participate in intervention design and implementation and to learn new skills and obtain job training to learn other ways to earn money. Both FSW and managers expressed dissatisfaction with government support: having to pay for clinic health exams, and managers expressed problems with the government’s ability to intervene around police raids and bribes. Conclusion: This project has the potential to improve HIV prevention research practices with FSWs by 1) foregrounding ethical issues by addressing barriers to respect, trust, and/or disclosure stemming from risks in the structural environment or micro-level social aspects of the research process and 2) developing a more transparent and participatory approach to HIV prevention research that engages participants/ FSWs in the research process in order to reduce perceived and actual risks to participants.

Selected recent publications and presentations:

Urada, L. (2013). Social and Structural Constraints on Disclosure and Informed Consent with Female Sex Workers and their Managers in the Philippines. JERHRE Special Issue (In Press).

Urada, L.A., Strathdee, S.A., Morisky, D.E., Schilling, R.F., Pimentel-Simbulan, N., Estacio Jr, L.R. & Raj, A. (2013). Sex work and its associations with alcohol and methamphetamine use among female bar and spa workers in the Philippines. Asia-Pacific Journal of Public Health. Online Jan. 22, 2013.

Urada, L.A., Morisky, D.E., Hernandez, L.I., & Strathdee, S.A. (2013). Social and structural factors associated with consistent condom use among female entertainment workers trading sex in the Philippines. AIDS and Behavior, 17(2), 523-535.

Urada, L.A., Raj, A., Cheng, D.M., Quinn, E., Bridden, C., Blokhina, E.A., Krupitsky, E., Samet, J.H. (in press). History of intimate partner violence is associated with sex work but not STI among HIV-positive female drinkers in Russia. International Journal of STD/AIDS.

Hiller, S. P., Urada, L. A., Lozada, R., Syvertsen, J., Ojeda, V. D. (in press). Social support and recovery among Mexican female sex workers who inject drugs. Journal of Substance Abuse Treatment.

Davtyan, M., Munoz, K., Urada, L., Brown, B. (accepted). Transactional sex- A client’s perspective from Peru. The Electronic Journal of Human Sexuality.

Urada, L.A., Goldenberg, S. M., Shannon, K., & Strathdee, S.A. (in press). Sex Work. In Baumeister, J., Ward, L. M., George, W., & Pfaus, J. (Eds.), APA Handbook of Sexuality. Washington, D.C.: American Psychological Association.

Urada, L.A., Strathdee, S.A., Morisky, D.E., Schilling, R.F., Pimentel-Simbulan, N., Estacio Jr, L.R. & Raj, A. (January, 2013). Sex work and its associations with alcohol and methamphetamine use among female bar and spa workers in the Philippines. Society for Social Work and Research Annual Conference, San Diego, CA.

Urada, L.A. (February, 2013). Disempowerment and engagement: Sex workers and female bar/spa workers in the Philippines. Panel on “Sexual health and empowerment of female sex workers in several countries” with Brown, B., Yarborough, D., & Swendenman, D. UC Global Health Day, UC Global Health Institute, Riverside, CA.

Urada, L.A., Goldenberg, S. M., Shannon, K., & Strathdee, S.A. (August, 2013). Sex Work. Panel on “Sexuality and social issues: Current advances and directions for the future” with Tolman, D., McClelland S. & Hernandez, K. American Psychological Association Convention, Honolulu, HI.

Urada, L.A. & Simmons, J. (November, 2013). Social and structural constraints on disclosure and informed consent with female sex workers and their managers in the Philippines. Panel on “Enhancing the responsible conduct of HIV prevention research across culturally and globally diverse populations” with Fisher C., Reed E., & Pearson C. American Public Health Association Annual Meeting and Exposition, Boston, MA.

Urada, L.A., Morisky, D.E., Pimentel-Simbulan, N., Silverman, J.G., & Strathdee, S.A. (2012). Condom negotiations among female sex workers in the Philippines: Environmental influences. PLoS ONE 7(3):1-9, doi: 10.1371/journal.pone.0033282. Epub 2012 Mar 20.

Urada, L.A., Malow, R.M., Santos, N.C., Morisky, D.E. (2012). Age differences among female sex workers in the Philippines: Sexual risk negotiations and perceived manager advice. AIDS Research and Treatment, doi: 10.1155/2012/812635. Epub 2012 Jul 17.

Cohort 2 Fellows

Tania Basta, Ph.D., M.P.H.

Consent Preparedness for Home-Based HIV Testing Research in Rural Appalachia

Abstract: BACKGROUND/RATIONALE: HIV rates are low in Appalachia, however individuals are engaging in high risk behaviors. Very few individuals get tested for HIV due to low HIV-related knowledge, high HIV-related stigma, and lack of access to testing sites. Home HIV testing kits will be available in October 2012 at Walmart, which will increase access for many rural individuals. SPECIFIC AIMS: AIM 1: Assess the knowledge and attitudinal factors that facilitate and hinder participation in HIV/STI prevention research among rural individuals living in Appalachia. AIM 2: Assess the effects of a brief educational intervention on theunderstanding of HIV acquisition, transmission and health effects, and the purpose, nature, risks and benefits, confidentiality protections, and voluntary nature of HIV/STI prevention research among rural individuals living in Appalachia. AIM 3: Assess the effects of a brief educational intervention on attitudes toward participation in HIV/STI prevention research among rural individuals living in Appalachia. STUDY POPULATION: The participants in this study will be residents of rural Appalachian counties in Ohio, West Virginia and Kentucky. Participants must be 18 years of age or older, live in a rural Appalachian county, do not have an HIV diagnosis, and speak fluent English. RESEARCH DESIGN: This study will be a mixed-methods study (focus groups, survey, and intervention) and will occur three phases.

Selected recent publications and presentations:

Basta, T. (2013, November). Factors influencing HIV testing among individuals living in rural Appalachia. In 141st APHA Annual Meeting (November 2-November 6, 2013). APHA.
             *Winner of the APHA Excellence in Abstract Submission among All Presentations Award.        

Bansah, A. K., Holben, D. H., & Basta, T. (2013). Food Insecurity is Associated with Household Utility Insecurity among Individuals Living with HIV/AIDS in Rural Appalachia. Journal of Hunger & Environmental Nutrition,8(2), 242-255.

Morrone, M., & Basta, T. B. (2013). Public opinion, local pollution havens, and environmental justice: a case study of a community visioning project in Appalachian Ohio. Community Development, (ahead-of-print), 1-14.

Darlington, K. A., Basta, T., & Obregon, R. (2012). Cross-generational relationships in rural Jamaica. Vulnerable Children and Youth Studies, 7(2), 128-138.

Morrone, M., Basta, T. B., & Somerville, J. (2012). Framing the national nuclear legacy at the local level: Implications for the future of federal facilities. Energy Policy, 43, 145-152.

Vance, R. A., Basta, T. B., Bute, J. J., & Denham, S. A. (2012). Identifying The Health Needs In Rural Appalachian Ohio: Outcomes Of A Rural Community-Academic Partnership. American Journal of Health Sciences (AJHS), 3(2), 115-124.

Brandon Brown, Ph.D., M.P.H.

Voluntary study participation in a clinical trial of HPV vaccine with Peruvian FSWs

Abstract: RESEARCH QUESTIONS: What do FSW participants understand about participation in a clinical trial, including study specifics, risks, benefits, and voluntariness? What are the effects of income, incentive types and amounts, and health care availability on voluntary participation in clinical trials with a certain level of risk? Can an incentive be excessive? BACKGROUND/RATIONALE: People should have voluntary choice to participate in a study. Informed consent may allow free choice, but measures to help ensure this during and after consent to gauge continued voluntariness and understanding of study participation are lacking. Understanding of acceptable/excessive incentive types and amounts is lacking, and study integrity may be brought into play if subjects falsify eligibility SPECIFIC AIMS: (1) Determine what FSWs understand/perceive about participating in a clinical trial, including study specifics, risks, benefits, and voluntariness; (2) Explore mediating effects of income, incentive types/amounts, and health care availability on voluntary participation of FSWs in clinical trials; and (3) Examine the issue of undue inducement in research, and if incentives and benefits are viewed as separate items. STUDY POPULATION: 40 FSWs in Peru previously in HPV vaccine trial. RESEARCH DESIGN: FG with 6-10 FSWs per group, 1-2 hrs, separated by income (brothel vs. street). Demographic info collected by survey.
Selected recent publications and presentations:

Brown, B., Blas, M. M., Heidari, O., Carcamo, C., & Halsey, N. A. (2013). Reported changes in sexual behaviour and human papillomavirus knowledge in Peruvian female sex workers following participation in a human papillomavirus vaccine trial. International journal of STD & AIDS, 24(7), 531-535.

Davtyan, M., Munoz, K., Urada, L., & Brown, B. (2013). Transactional Sex: A Client’s Perspective from Peru. Electronic Journal of Human Sexuality, 16.

Nureña, C. R., Brown, B., Galea, J. T., Sánchez, H., & Blas, M. M. (2013). HPV and Genital Warts among Peruvian Men Who Have Sex with Men and Transgender People: Knowledge, Attitudes and Treatment Experiences. PloS one, 8(3), e58684.

Shroff, N., Brown, B., Kinsler, J., Cabral, A., & Blas, M. M. (2013). Barriers and Facilitators in the Recruitment and Retention of Peruvian Female Sex Workers in a Randomized HPV Vaccine Trial. J Vaccines Vaccin, 4(198), 2.

Brown, B., Davtyan, M., Galea, J., Chow, E., Leon, S., & Klausner, J. D. (2012). The Role of Human Papillomavirus in Human Immunodeficiency Virus Acquisition in Men who Have Sex with Men: A Review of the Literature.Viruses, 4(12), 3851-3858.

Brenda Curtis, Ph.D.

Online Recruiting for HIV Research: Ethical Issues and Concerns for Investigators and IRBs

Abstract: RESEARCH QUESTION: What ethical dilemmas have arisenduring the design and conduct of HIV prevention research that used Internet recruitment? BACKGROUND/RATIONALE: Institutional Review Boards (IRBs) are facing major challenges in the research environment due to changes in how investigators recruit human subjects. SPECIFIC AIMS: To examine the ethical challenges investigators and IRBs have encountered in developing adequate human subjects protections for recruitment procedures for HIV prevention. To provide examples of how these dilemmas were resolved by investigators and IRBs. STUDY POPULATION: PHS Funded Principal Investigators and IRB chairs at academic institutions. RESEARCH DESIGN: Semi-structured phone interviews will be conducted with 15 IRB Chairs/Directors and 15 HIV prevention principal investigators.

Selected recent publications and presentations:

Conducting a workshop using data obtained from this research project at the PRIM&R 2013 Advancing Ethical Research (AER) Conference in Boston.  

Presented at PRIM&R 2013.

Curtis, B. (2013). Online Recruiting for HIV Research: New Challenges for Institutional Review Boards. JERHRE Special Issue (In Press).

Shira Goldenberg, Ph.D.

Barriers and Facilitators to Participation in HIV Research: Female Sex Workers’ Perspectives

Abstract: BACKGROUND/RATIONALE: Research with female sex workers (FSWs) is critical to inform prevention; few data on barriers and facilitators to participation. SPECIFIC AIMS: (1) Investigate perceived barriers and facilitators to participation. (2) Develop recommendations to enhance FSWs’ participation. STUDY POPULATION: FSWs ≥18 years old in Tecun Uman/Xela. RESEARCH DESIGN: 3-5 focus groups + follow-up interviews (min. n=5). IMPACT: Development of interventions to address barriers & facilitators and enhanced ethical practices in sex work research.
Selected recent publications and presentations:

Goldenberg, S. M., Engstrom, D., Rolon, M. L., Silverman, J. G., & Strathdee, S. A. (2013). Sex Workers Perspectives on Strategies to Reduce Sexual Exploitation and HIV Risk: A Qualitative Study in Tijuana, Mexico. PloS one,8(8), e72982.

Goldenberg, S. M., Chettiar, J., Simo, A., Silverman, J. G., Strathdee, S. A., Montaner, J., & Shannon, K. (2013). Early sex work initiation independently elevates odds of HIV infection and police arrest among adult sex workers in a Canadian setting. Journal of acquired immune deficiency syndromes (1999).

Collins, S. P., Goldenberg, S. M., Burke, N. J., Bojorquez-Chapela, I., Silverman, J. G., & Strathdee, S. A. (2013). Situating HIV risk in the lives of formerly trafficked female sex workers on the Mexico–US border. AIDS care,25(4), 459-465.

Knight, R., Shoveller, J. A., Oliffe, J. L., Gilbert, M., & Goldenberg, S. (2013). Heteronormativity hurts everyone: Experiences of young men and clinicians with sexually transmitted infection/HIV testing in British Columbia, Canada.Health:, 17(5), 441-459.

Goldenberg, S. M., Strathdee, S. A., Perez-Rosales, M. D., & Sued, O. (2012). Mobility and HIV in Central America and Mexico: A critical review. Journal of Immigrant and Minority Health, 14(1), 48-64.

Goldenberg, S. M., Rangel, G., Vera, A., Patterson, T. L., Abramovitz, D., Silverman, J. G., ... & Strathdee, S. A. (2012). Exploring the impact of underage sex work among female sex workers in two Mexico–US border cities.AIDS and Behavior, 16(4), 969-981.

Thomas Guadamuz, Ph.D., M.H.S.

Barriers and facilitators to YMSM participating in HIV-related research studies in Thailand: Perspectives of parents and teens

Abstract: RESEARCH QUESTION: What are the barriers and facilitators to YMSM (under 18 years) participating in HIV-related research studies in Thailand? BACKGROUND/RATIONALE: Young men who have sex with men (YMSM) continue to bear the burden of new HIV infections in Southeast Asia. Currently, there are very few studies that include YMSM under 18 years. Reasons for not including YMSM in research studies include the requirements of parental consent from IRBs. This resents a problem because many YMSM have not disclosed their sexual activities or sexual orientation identities to their parents. SPECIFIC AIMS: To examine the barriers and facilitators related to the participation of YMSM in HIV-related research studies from the perspectives of parents  and teens. STUDY POPULATION: Using purposive sampling, 6 groups of parents and YMSM will be recruited: (1) Parents of sons, (2) parents of gender non-conforming YMSM, (3) parents of “out”/disclosed YMSM, (4) “out” /disclosed YMSM (15-17 years), (5) “not out” YMSM (18-20 years), (6) street-based YMSM. RESEARCH DESIGN: Qualitative research methods: Focus group discussions and semi-structured in-depth interviews (5-8 persons per group above and 1-2 persons per FGD will be asked to participate in in-depth interviews). A total sample size of 50 is expected. Social and cultural values and related issues specific to the Thai context will be explored in detail. IMPACT: To reduce the barriers of adolescent participation in sexuality-related research in Thailand.

Selected recent publications and presentations:   

Guadamuz, T. E., Friedman, M. S., Marshal, M. P., Herrick, A. L., Lim, S. H., Wei, C., & Stall, R. (2013). Health, Sexual Health, and Syndemics: Toward a Better Approach to STI and HIV Preventive Interventions for Men Who Have Sex with Men (MSM) in the United States. In The New Public Health and STD/HIV Prevention (pp. 251-272). Springer New York.

Guadamuz, T. E., Lim, S. H., Marshal, M. P., Friedman, M. S., Stall, R. D., & Silvestre, A. J. (2012). Sexual, Behavioral, and Quality of Life Characteristics of Healthy Weight, Overweight, and Obese Gay and Bisexual Men: Findings from a Prospective Cohort Study. Archives of sexual behavior, 41(2), 385-389.

Herrick, A. L., Lim, S. H., Plankey, M. W., Chmiel, J. S., Guadamuz, T. T., Kao, U., ... & Stall, R. (2013). Adversity and syndemic production among men participating in the Multicenter AIDS Cohort Study: a life-course approach.American journal of public health, 103(1), 79-85.

Wei, C., Lim, S. H., Guadamuz, T. E., & Koe, S. (2013). Virtual Versus Physical Spaces: Which Facilitates Greater HIV Risk Taking Among Men Who Have Sex with Men in East and South-East Asia?. AIDS and Behavior, 1-8.

Lim, S. H., Guadamuz, T. E., Wei, C., Chan, R., & Koe, S. (2012). Factors associated with unprotected receptive anal intercourse with internal ejaculation among men who have sex with men in a large internet sample from Asia. AIDS and Behavior, 16(7), 1979-1987.

Wei, C., Guadamuz, T. E., Lim, S. H., Huang, Y., & Koe, S. (2012). Patterns and levels of illicit drug use among men who have sex with men in Asia. Drug and alcohol dependence, 120(1), 246-249.

Wei, C., Lim, S. H., Guadamuz, T. E., & Koe, S. (2012). HIV disclosure and sexual transmission behaviors among an Internet sample of HIV-positive men who have sex with men in Asia: Implications for prevention with positives. AIDS and Behavior, 16(7), 1970-1978.

Wei, C., Guadamuz, T. E., Lim, S. H., & Koe, S. (2012). Sexual transmission behaviors and serodiscordant partnerships among HIV-positive men who have sex with men in Asia. Sexually transmitted diseases, 39(4), 312.

Charmaine Thokoane

Knowledge of rights to sexual reproductive health services among 12-18 year olds in Hammanskraal

Abstract: INTERVENTION PROGRAM QUESTIONS: What are the attitudes of youth regarding their rights to access sexual and reproductive health services? What is the knowledge that the youth has regarding their rights to sexual and reproductive health services? What are the attitudes of the health workers that create a barrier for the youth in accessing sexual and reproductive health services? STUDY POPULATION: 40 young people (12-18 year olds) out of school and in-school recruited at local NGO’s and through referrals by other youth. Health care workers recruited from hospital and clinics. EVALUATION DESIGN: Youth: Pre-study circle intervention questionnaire, study circle, post-study circle questionnaire. Health Care Workers: In depth interviews, pre intervention interview, training on working with young people, post intervention interview.

Kristen Underhill, J.D., Ph.D.

Exploring IRB Responses to Participant Complaints: Processes, Values, and Resources

Abstract: RESEARCH QUESTION: How do IRBs respond to participant complaints arising out of general clinical research and PrEP effectiveness studies?  BACKGROUND/RATIONALE: Participants in clinical research are advised to contact IRBs with questions or complaints, but little scholarship has examined IRBs’ procedures for responding.  SPECIFIC AIMS: To use qualitative methods to explore (1) How IRBs may address risk of side effects, HIV infection, secondary resistance, and posttrial access when approving PrEP effectiveness protocols. (2) Procedures that IRBs currently use to respond to participant complaints. (3) How IRBs may apply dispute resolution procedures to complaints in PrEP trials. (4) What guidance or training IRBs may need to guide these processes.  STUDY POPULATION: IRB chairs, directors, and possible IRB-related legal personnel from IRBs thatreview PrEP clinical trials.  RESEARCH DESIGN: Individual semi-structured qualitative interviews, triangulated with documentation of IRB policies or procedures.

Selected recent publications and presentations:

Underhill, K. (2013). Legal Issues in Addressing Participant Complaints Arising from Biomedical HIV Prevention Trials: How Can IRBs Respond?. JERHRE Special Issue. (In Press).

Underhill, K. (2013). Study designs for identifying risk compensation behavior among users of biomedical HIV prevention technologies: Balancing methodological rigor and research ethics. Social Science & Medicine.

Underhill, K. (2013). Risk-Taking and Rulemaking: Addressing Risk Compensation Behavior Through FDA Regulation of Prescription Drugs. Yale J. on Reg., 30, 377-475.

Underhill, K. (2013). Transferring Behavioral Interventions for Global Health: Intellectual Property Barriers, Information Constraints, and Possible Solutions. Yale Journal of Health Policy, Law, and Ethics, 10(2), 3.

Underhill, K. (2012). Paying for prevention: challenges to health insurance coverage for biomedical HIV prevention in the United States. Am. JL and Med.,38, 607-751.

Cohort 3 Fellows
Stella Njuguna, B. Pharm., M.P.H.

Post-trial access of Truvada® amongst HIV-1 discordant couples enrolled in the PrEP study in Kisumu, Kenya

NATURE OF THE PROBLEM: In Kenya, 44% of married/cohabitingHIV infected persons have an HIV uninfected partner. This population of HIV sero-discordant couples contributes significantly to the incidence HIV infections in the country. Given the high risk of transmission, novel HIV prevention strategies are critical in decreasing the incidence of HIV infection. HIV RESEARCH ETHICS QUESTION: Recent trialshave proven that Truvada is efficacious in preventing the acquisition of HIV.  One such trial of sero discordant couples was conducted in Kisumu, Kenya. However, participants do not have post trial access (PTA) to Truvada. Who is responsible for PTA in this population? This is a critical ethical issue that needs to be addressed. BACKGROUND/RATIONALE: The global burden of HIV epidemic is greatest in Sub-Saharan Africa. In Kenya, the HIV prevalence is approximately 7.4% with wide geographic variations of the epidemic. Nyanza province has the highest HIV prevalence of 15.3%. In Kenya, 44% of married/cohabiting HIV infected persons have an HIV uninfected partner and this population contributes significantly to the incidence HIV infections in the country. Given the high risk of transmission in this population, novel HIV prevention strategies are critical in decreasing the incidence of HIV infection. Recent studies have shown that Truvada is efficient in preventing HIV infections in most at risk populations. However, Truvada has not been availed to the participants who were enrolled in the Pre-Exposure Prophylaxis (PrEP) study in Kisumu, Kenya. This is a critical ethical issue embodied in the principle of distributive justice that needs to be addressed.  STUDY OBJECTIVES: the goal of this study is to examine attitudes regarding post-trial access to Truvada amongst a random sample of sero-discordant couples previously enrolled in the PrEP study in Kisumu, Kenya. Specifically we seek to: 1. explore participants views about PTA  to Truvada; and 2. identify potential  delivery of Truvada to the couples. STUDY POPULATION: HIV sero-discordant couples formerly enrolled in the PrEP study Kisumu. RESEARCH DESIGN/PROPOSED MEASURES: This is a mixed method cross sectional study where qualitative and quantitative data will be collected. Focus group discussions (FGD) conducted by an experienced moderator will explore views and probe for information regarding post-trial access to Truvada from former PrEP study participants. We will conduct two FGDs of a random sample of HIV-1discordant couples. Each FGD will be gender specific and be composed of eight to ten HIV-negative women and men. In-depth interviews will also be conducted for the research participants who seroconverted during the study period to explore the attitudes, opinions and feelings about PTA. FGD guides and interview scripts will be piloted tested prior use. Each FGD and interview will be audio recorded and later transcribed and translated for analysis. Field notes will also be taken during the FGDs and interview sessions. Finally, a brief questionnaire will be administered to participants to capture their socio-economic demographics and trial experience. Informed consent will be sought from study participants’ prior data collection.

Nicole Overstreet, Ph.D.

Assessing the role of stigma on women’s participation in and perceptions of intimate partner violence research

NATURE OF THE PROBLEM: Women who experience intimate partner violence (IPV) are susceptible to HIV infection through several HIV risk factors, including sexually transmitted infections, sexual risk-taking behaviors, and mental health correlates of HIV risk, such as depression and posttraumatic stress disorder. As researchers move toward incorporating IPV into HIV prevention efforts, it is necessary to consider empirically supported ethical research practices among this population. A primary ethical concern in IPV research is nonmaleficience—an ethical principle that asserts that research should minimize harm to research participants. Research has largely focused on understanding whether participation in IPV research increases participants’ distress when answering trauma-focused questions; however, this line of research tells us very little about whether the experience of participating in IPV research elicits concerns about stigma, whether this stigma shapes research participation, and whether this stigma negatively influences research participants during study participation. HIV RESEARCH ETHICS QUESTION: The proposed study examines how stigma influences women’s participation in IPV research, whether stigma threatens the goal of nonmaleficience, and factors that heighten stigma during the research process. BACKGROUND/RATIONALE: Stigma is an important factor to consider when conducting empirical ethical research on IPV. Among other vulnerable populations (e.g., substance users, people living with mental illness), researchers have outlined how stigma influences fears about the consequences of a breach in confidentiality, heightens concerns about privacy issues, shapes how comfortable participants’ feel about responding candidly to research questions, and limits whether people participate in treatment and intervention research. In the IPV literature, stigma has rarely been the focus of ethics research despite the pervasiveness of stigma in the lives of women who experience IPV. Stigma associated with IPV may impact various aspects of the research process: women may fear placing their names on consent forms because of concerns about stigmatizing consequences related to breaches in confidentiality, such as being found by partners who assaulted them and being further stigmatized because of one’s victim status. Concerns about stigma may become exacerbated when IPV research intersects with HIV prevention research in which women discuss sensitive topics related to HIV risk that are also stigmatized in society, such as trading sex for money/housing or drug abuse. Thus, it is important to empirically examine the nuanced ways that stigma shapes ethical concerns in IPV research. SPECIFIC AIMS: 1) To examine whether anticipated stigma and internalized stigma associated with IPV affects decisions to participate in IPV research; 2) To examine women’s concerns about stigmatizing consequences during the research process (e.g., confidentiality risks, risk of further violence, risk of experiencing internalized stigma); 3) To examine whether stigma experienced during the research process shapes women’s responses to sensitive questions; 4) To examine factors that heighten stigma during the research process (e.g., psychological distress, method of recruitment) STUDY POPULATION: Women in the New Haven area who experienced IPV with a male partner who was arrested and arraigned in a domestic violence case. RESEARCH DESIGN AND PROPOSED MEASURES: Mixed-methods approach with semi-structured interviews and survey questions.

Alexis Roth, Ph.D., M.P.H.

Ethical considerations for mHealth research collecting sensitive information among people who inject drugs

NATURE OF THE PROBLEM: Research has shown drug use varies day-to-day, and even hour-by-hour, based on individual, social, and structural phenomena. However, traditional epidemiological methods for assessing drug use and related HIV risk behavior rely on participant recall thereby eliciting generalized patterns of behavior, rather than event-level information. Retrospective reporting is likely to result in under or over estimation of the true frequency of behaviors depending on several factors, including actual frequency, social desirability, and contextual factors surrounding these events. Thus, tools that capture greater granularity are needed to better understand polydrug use among PWID. BACKGROUND/RATIONALE FOR THE STUDY: Electronic diaries, a tool for conducting ecological momentary assessments (EMA), can capture highly-specific event-level data. To be considered feasible, EMA studies strive for approximately 80% compliance to study protocol. This protocol is often quite burdensome, cueing participants to respond to behavioral assessments 2-5 times per day. Several ethical issues arise by virtue of frequent assessment. Appropriate compensation for participation mustbe considered.  EMA studies tend to provide fairly generous compensation with a combination of payment per diary entry, personal use of a mobile device, and/or ability to retain the device upon successful study completion. Drug users may be financially unable to decline study participation. Thus, an ethical dilemma may arise from selecting a compensation structure sufficient to encourage adherence to a highly-demanding protocol without coercing consent. Additional concerns include understanding the unanticipated benefits and potential consequences of involvement in diary studies. For example, is assessing drug craving a trigger for drug use? How should researchers act when sensitive, illegal, or potentially harmful information outside of the expressed study purpose is discovered? What concerns might participants have about privacy and data security? Answers to these and related questions are critical for designing ethical studies that use electronic diaries to collect sensitive behavioral information from substance abusers. HIV RESEARCH ETHICS QUESTION: What are the human subjects concerns of individuals participating in an EMA study of polydrug use? STUDY POPULATION: This study will be embedded within a longitudinal cohort study of PWIDs in San Diego, California (STAHR II; PI: Garfein, R01 031074). RESEARCH DESIGN AND PROPOSED MEASURES: The present study will utilize theatre testing and qualitative methods to develop an EMA study of polydrug use. Participants (N = 30) will complete a cell phone-delivered electronic diary assessing contextual determinants of polysubstance use and key related health outcomes (. They will then complete a qualitative interview. Using open-ended questions, I will assess key aspects of their participation experience. Specific probes will be used to explore key ethical issues including compensation, penalties for non-adherence, frequency of contact with research staff, concerns about confidentiality and data security, possibility of physical harm from carrying a study-provided cell phone, and psychological harm from diary assessments. SPECIFIC AIMS: 1) To describe participant perspectives on the use of mobile technology to assess sensitive behaviors; and 2) To design a participant-informed EMA protocol.

Darpun Sachdev, M.D.

The ethical provision of PrEP in a multi-national HIV vaccine efficacy study

NATURE OF THE PROBLEM:  Within the field of HIV vaccine research, the efficacy of PrEP supports the concept that a preventive vaccine does not need to be “100% effective” and offers hope that a vaccine and PrEP combination could have synergistic effects.  In considering the design of future HIV vaccine efficacy trials, researchers must determine how PrEP should be offered as part of the clinical trials. HIV RESEARCH ETHICS QUESTION:  1) What is the standard of prevention package in each of these communities and what are the unmet needs, 2) How do we implement one protocol in many countries with differing standards of prevention care?, and 3) If PrEP is offered as part ofupcoming trials, what will post-trial access to PrEP look like?  BACKGROUND/RATIONALE FOR THE STUDY:  After the findings from a large PrEP trial were announced in 2011, the protocol team of HVTN 505, evaluated whether to include PrEP as part of the ongoing Phase 2b vaccine efficacy trial among men who have sex with men in the United States.  The core questions were: 1) Is PrEP part of the “standard of HIV prevention” in the United States, and 2)  Does the study needed to be modified based on this change?    The key drawback of including PrEP in vaccine trials is that the provision of PrEP increases the sample size necessary to achieve the same number of HIV seroconversion endpoints. As ongoing clinical trials respond to changing standards of HIV prevention care and new multi-national HIV vaccine trials are designed, it is essential to address ethical questions regarding PrEP provision in the context of vaccine efficacy studies. SPECIFIC AIMS: 1) To determine if PrEP is part of the standard of HIV prevention care in San Francisco, Atlanta,Peru and Brazil, 2) To determine community perspective regarding the  priorities, benefits and concerns of providing PrEP as part of a vaccine efficacy trial. STUDY POPULATION: Ethicists, study investigators, CAB members, and community members in San Francisco, Atlanta, Peru and Brazil.  RESEARCH DESIGN AND PROPOSED MEASURES: A mixed-methods study will be conducted in San Francisco, Atlanta, Lima, and Sao Paolo.  The study will consist of 2 phases. In Phase 1, we will understand the current local standard of HIV prevention and determine how PrEP fits into the prevention package.  We will conduct individual qualitative interviews with ethicists, site investigators, CAB members.  We will analyze data on what has been offered at various trial sites to date, how this was justified, and what were the perceived consequences of this in terms of both short- and long-term health benefits for trial participants and their communities.  In Phase 2, we will collect data from the community regarding the priorities, benefits and concerns of providing PrEP as part of a prevention trial.  We plan to conduct two focus groups of approximately 6-8 individuals at each of the 4 sites.   The focus groups will include a short presentation that illustrates a hypothetical vaccine trial.  We will analyze data on participant responses to proposed trial scenarios.

Andrew Spieldenner, Ph.D.

Ethical dimensions in the increased involvement of Black and Latino men who have sex with men (MSM) in HIV Pre-Exposure Prophylaxis (PrEP) clinical research

NATURE OF THE PROBLEM:HIV Pre-Exposure Prophylaxis (PrEP) has emerged as a viable HIV prevention tool, yet there is still much to learn about the intervention. While research is ongoing in the US in San Francisco and Miami, the FDA has approved PrEP for usage based on physician-prescription (Cohen et al., 2013). Previous research has demonstrated that research participation for African Americans and Latinos can be increased through two tools: more effective pre-screening tools and enhanced education on research at the point of informed consent (Kneipp et al, 2009; Raich et al., 2010). These are connected concepts, and happen early in the recruitment process. Previous research haslooked at pre-screening for heterosexual African Americans and Latinos (Cortes et al., 2010), and health research education for heterosexual African Americans to increase research participation (Dunlop et al., 2010). HIV RESEARCH ETHICS QUESTION: This project explores pre-screening tools and health research education in the context of PrEP for Black and Latino gay men in New York City. BACKGROUND/RATIONALE: Due to the disproportionate impact of HIV on Black and Latino gay men, more research is needed on PrEP in these communities (Dutta, 2013). Research in this area has focused on other HIV biomedical interventions (e.g. vaginal microbicides, circumcision), but there is a dearth of information on the needs of Black and Latino gay men. SPECIFIC AIMS: The specific aims will be to develop appropriate pre-screening tools, and to enhance informed consent with education on health research in order to increase participation in HIV PrEP research. STUDY POPULATION: The study population will be Black and Latino gay men living in New York City. For the purpose of this study, participants can be HIV-negative or HIV-positive (if in a sero-discordant relationship). RESEARCH DESIGN AND PROPOSED MEASURES: Eight focus groups with Black and Latino gay men will be conducted throughout the coming year (Smith et al., 2012). Focus groups are useful to determine community norms and to observe interactions amongst group participants. This can be especially useful in eliciting information from individuals whose cultural norms include backchannel talk and group conversations, including Latino and Black gay men (Saint-German et al., 1993). The focus groups will include discussion questions around: PrEP to ascertain basic knowledge and provide context for health research, and pre-screening concerns (e.g. invasiveness, enough information, motivate to participate). In addition, the informed consent process will be role played to the focus group, and participants will be asked to respond to the process for clarity, trust and improvement (Barata et al., 2006).

Sean Young, Ph.D.

Ethics and Social Networking for HIV Research

NATURE OF THE PROBLEM: A number of ethical issues exist related to how social networking technologies should be used for HIV prevention-related interventions. However, no research has examined how participants describe these ethical issues or documented recommendations throughout the process of recruitment to follow-up. HIV RESEARCH ETHICS QUESTION: What are the ethical issues involved in social media for HIV prevention research, from recruitment to study follow-up? What are participant concerns when participating in social networking for HIV prevention research? What recruitment, intervention, and follow-up methods should be used during an HIV intervention based on social networking platforms? BACKGROUND/RATIONALE: In a number of studies, we have discovered ways that social networking technologies can be used for HIV prevention research. Although we have the ability to ask participants from these studies about their experiences to help uncover and address potential ethical issues, participants have not been surveyed on these topics. It is important that we recontact past participants to find out about their experiences in order to understand the ethical issues associated with social networking for HIV prevention research and how to design future studies that take into account these ethical challenges. SPECIFIC AIMS: 1) Hypothesize about potential ethical issues involved when using social networking technologies for HIV prevention among at-risk populations. 2) Contact past participants to learn their attitudes and perspectives on having participated in the study and survey them about ethical issues related to study participation. 3) Document the ethical issues that need to be addressed when conducting HIV prevention research using social networking technologies and propose solutions to these issues. STUDY POPULATION: Fifteen men who have sex with men (primarily African American and Latino) who have previously been involved in our own social networking for HIV prevention research studies on Facebook. RESEARCH DESIGN AND PROPOSED MEASURES: Participants will be invited to join an online focus. The focus group will take place over 2 sessions and will have modules to describe the processes involved in social networking for HIV prevention research (e.g., recruitment, informed consent, intervention, follow-up). Participants will receive quantitative questionnaires designed to assess their attitudes and experiences using social networking for HIV prevention, such as concerns about public recruitment and visible information in social networking groups, methods of contact and follow-up, and survey methodology. Data will be collected and used to document ethical issues in using social networking for HIV prevention research and how to address participant concerns during the intervention process.

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