Health-care facilities

Abdool Karim, Q., Abdool Karim, S. S., Coovadia, H. M., & Susser, M. (1998). Informed consent for HIV testing in a South
African hospital: Is it truly informed and truly voluntary?
. American Journal of Public Health, 88(4), 637-640.
Informed consent (adults), Voluntariness and self-efficacy, Adults (other), People living with HIV, People at risk for or with other STIs, Survey research, Health-care facilities, South Africa, Quantitative (QT)

Akkad, A., Jackson, C., Kenyon, S., Dixon-Woods, M., Taub, N., & Habiba, M. (2006). Patients’ perceptions of written consent: questionnaire study. BMJ: British Medical Journal, 333(7567), 528.
Informed consent (adults), Adults (other), Survey research, Health-care facilitiesEnglandQuantitative (QT)

Barnett, P. G., Hall, S. M., Haug, N. A., Sorensen, J. L., & Wong, W. (2008). Effect of incentives for medication adherence on health care use and costs in methadone patients with HIV. Drug Alcohol Dependence, 1, 115-121.
Research risks and benefitsPeople living with HIVPeople who inject drugsClinical trialsHealth-care facilitiesUnited StatesQuantitative (QT)

Basta, T. B., Stambaugh, T., & Fisher, C. B. (2014). Efficacy of an educational intervention to increase consent for HIV testing in rural Appalachia. Ethics and Behavior, 25 (2), 129-145.
Confidentiality and privacyInformed consent (adults)Research risks and benefitsPeople at risk for HIVPeople at risk for or with substance use addictionsClinical trials, Health-care facilities, United States 

Brooks, R. A., Newman, P. A., Duan, N., & Ortiz, D. J. (2007). HIV vaccine trial preparedness among Spanish-speaking Latinos in the US. AIDS Care, 19(1), 52-58.
Research risks and benefits, Research trust and mistrust, Stigma, People at risk for HIV, Clinical trials, Community organizations, Health-care facilities, United States, Qualitative (QL)

Brown, E. J. & Hill, M. A. (2005). Perceptions of HIV risks and prevention strategies by rural and small city African Americans who use cocaine: Views from the inside. Issues in Mental Health Nursing, 26, 359-377.
Multicultural competence, Research risks and benefits, People at risk for HIV, People at risk for or with substance use addictions, Community-engaged research, Community organizations, Health-care facilities, United States, Qualitative (QL)

Chaisson, L. H., Kass, N. E., Chengeta, B., Mathebula, U., & Samandari, T. (2011). Repeated assessments of informed consent comprehension among HIV-infected participants of a three-year clinical trial in Botswana. PloS one,6(10), e22696.
Informed consent (adults), Multicultural competence, Research risks and benefits, Clinical trials, Government agencies, Health-care facilities, BotswanaQuantitative (QT)

Chenneville, T., Lynn, V., Peacock, B., Turner, D., & Marhefka, S. L. (2015). Disclosure of HIV status among female youth with HIV. Ethics and Behavior, 25 (4), 314-331.
StigmaAdolescentsPeople living with HIV, Health-care facilitiesSurvey researchUnited States, Qualitative (QL)

Cohn, J. M., Ginsburg, K. R., Kassam-Adams, N., & Fein, J. A. (2005). Adolescent decisional autonomy regarding participation in an emergency department youth violence interview. The American Journal of Bioethics, 5(5), 70-74.
Assent and self-consent (children and adolescents), Voluntariness and self-efficacy,Adolescents, Victims of interpersonal violence, Survey research, Health-care facilities, United StatesQuantitative (QT)

Deng, J., Qian, M., Gan, Y., Hu, S., Gao, J., Huang, Z., & Zhang, L. (2015). Emerging practices of counseling and psychotherapy in China: ethical dilemmas in dual relationships. Ethics and Behavior, 26 (1), 63-86.
Multicultural competenceResearch misconductTherapeutic misconceptionAdults (other)Survey researchHealth-care facilitiesChinaQualitative (QL)

Eisingerich, A. B., et al. (2012). Attitudes and Acceptance of Oral and Parenteral HIV Preexposure Prophylaxis among Potential User Groups: A Multinational Study. PLoS ONE 7(1): e28238.
Research risks and benefits, Stigma, Adults (other), People at risk for HIV, People at risk for or with other STIs, People involved in sex work, People who inject drugs, Sexual and gender minorities, Community-engaged research, Community organizations, Health-care facilities, Botswana, India, Kenya, Peru, South Africa, Uganda, UkraineQuantitative (QT)

El-Wakeel, H., Taylor, G. J., & Tate, J. J. T. (2006). What do patients really want to know in an informed consent procedure? A questionnaire-based survey of patients in the Bath area, UK. Journal of medical ethics, 32(10), 612-616.
Informed consent (adults), Research risks and benefits, Adults (other), Clinical trials,Survey research, Health-care facilities, EnglandQuantitative (QT)

Festinger, D. S., Arabia, P. L., Croft, J. R., Dugosh, K. L., & Marlowe, D. B. (2008). Higher magnitude cash payments improve research follow-up rates without increasing drug use or perceived coercion.  Drug Alcohol Dependence, 96 (1-2), 128-135.
Research risks and benefitsVoluntariness and self-efficacyPeople at risk for HIV, People at risk for or with other STIs, People at risk for or with other substance abuse addictionsPeople who inject drugs, Clinical trials, Health-care facilitiesUnited StatesQuantitative (QT)

Flynn, K. E., Weinfurt, K. P., Seils, D. M., Lin, L., Burnett, C. B., Schulman, K. A., & Meropol, N. J. (2008). Decisional conflict among patients who accept or decline participation in phase I oncology studies. Journal of empirical research on human research ethics: JERHRE, 3(3), 69-77.
Research risks and benefits, Voluntariness and self-efficacy, Adults with other health problems, Clinical trials, Health-care facilities, United StatesQuantitative (QT)

Forman, R. F., Bovasso, G., Clark, C., McNicholas, L., Royer-Malvestuto, C., Weinstein, S., & Woody, G. (2002). Staff beliefs about drug abuse clinical trials.  Journal of Substance Abuse Treatment, 23 (1), 55-60.
Therapeutic misconceptionVoluntariness and self-efficacyAdults (other), Clinical trialsEthics educationHealth-care facilitiesUnited StatesQuantitative (QT)

Franrenet, S., Moutel, G., Raffi, F., Dabis, F., Bruyand, M., Hervé, C., & … Duchange, N. (2011). Information that should be given to HIV cohort participants during ongoing research: The viewpoints of patient representatives and research professionals. Journal Of Empirical Research On Human Research Ethics, 6(4), 76-83.
Investigator practices and perspectives, Adults (other)People at risk for or living with other STIs, People living with HIV, Clinical trials, Health-care facilities, France, Mixed methods (MM)

Fuchs, J., Durham, M., McLellan-Lemal, E., Vittinghoff, E., Colfax, G., Gurwith, M., & Buchbinder S. (2007). Negative social impacts among volunteers in an HIV vaccine efficacy trial. Journal of Acquired Immune Deficiency Syndromes, I, 362-368.
Research risks and benefits, Stigma, People at risk for HIV, Clinical trials, Health-care facilities, United States, Quantitative (QT)

Garber, M., Hanusa, B. H., Switzer, G. E., Mellors, J., & Arnold, R. M. (2007). HIV-infected African Americans are willing to participate in HIV treatment trials. Journal of General Internal Medicine, 22(1), 17-42.
Multicultural competence, Voluntariness and self-efficacy, People living with HIV, Clinical trials, Health-care facilities, United States, Quantitative (QT)

Groves, A. K., Maman, S., Msomi, S., Makhanya, N., & Moodley, D. (2010). The complexity of consent: Women’s experiences testing for HIV at an antenatal clinical in Durban, South Africa. AIDS Care, 22(5), 538-544.
Informed consent (adults), Voluntariness and self-efficacy, People at risk for HIV, Health-care facilities, South Africa, Qualitative (QL)

Haire, B. (2013). Ethics of Medical Care and Clinical Research: A Qualitative Study of Principal Investigators in Biomedical HIV Prevention Research. Journal Of Medical Ethics: The Journal Of The Institute Of Medical Ethics, 39(4), 231-235.
Investigator practices and perspectives, Investigators, Research staff, Clinical trials, Health-care facilities, Australia, Qualitative (QL)

Hall, M. A., Camacho, F., Lawlor, J. S., DePuy, V., Sugarman, J., & Weinfurt, K. (2006). Measuring trust in medical researchers. Medical care, 1048-1053.
Confidentiality and privacy, Research trust and mistrust, Voluntariness and self-efficacy,Adults (other), Survey research, Health-care facilities, United StatesQuantitative (QT)

Hamm, M., Scott, S., Klassen, T., Moher, D., & Hartling, L. (2012). Do health care institutions value research? A mixed methods study of barriers and facilitators to methodological rigor in pediatric randomized trials. BMC medical research methodology, 12(1), 158.
Assent and self-consent (children and adolescents), Investigator practices and perspectives, Investigators, Research staff, Clinical trials, Health-care facilities,CanadaMixed methods (MM)

Hazen, R. A., Eder, M., Drotar, D., Zyzanski, S., Reynolds, A. E., Reynolds, C. P., …& Noll, R. B. (2010). A feasibility trial of a video intervention to improve informed consent for parents of children with leukemia. Pediatric blood & cancer, 55(1), 113-118.
Informed consent (adults), Parents, Clinical trials, Health-care facilities, United StatesQuantitative (QT)

Hickman, N. J., Prochaska, J.J., & Dunn, L. B. (2011). Screening for understanding of research in the inpatient psychiatry setting. Journal of Empirical Research on Human Research Ethics, 6(3), 65-72.
Informed consent (adults), Research risks and benefits, Adults with mental health disorders, Clinical trials, Health-care facilities, United States, Quantitative (QT)

Joffe, S., Cook, E. F., Cleary, P. D., Clark, J. W., & Weeks, J. C. (2001). Quality of informed consent: a new measure of understanding among research subjects. Journal of the National Cancer Institute, 93(2), 139-147.
Informed consent (adults), Adults with other health problems, Clinical trials, Health-care facilities, United States, Quantitative (QT)

Joffe, S., Cook, E. F., Cleary, P. D., Clark, J. W., & Weeks, J. C. (2001). Quality of informed consent in cancer clinical trials: a cross-sectional survey. Lancet, 358(9295), 1772-1777.
Informed consent (adults), Therapeutic misconception, Adults with health problems, Clinical trials, Health-care facilities, United StatesQuantitative (QT)

Kassam-Adams, N., & Newman, E. (2002). The reactions to research participation questionnaires for children and for parents (RRPQ-C and RRPQ-P). General Hospital Psychiatry, 24(5), 336-342.
Assent and self-consent (children and adolescents), Children, Parents, Clinical trials,Survey research, Health-care facilities, United StatesQualitative (QL)

Kassam-Adams, N. Newman, E. (2005). Child and parent reactions to participation in clinical research. General Hospital Psychiatry, 27(1), 29-35.
Assent and self-consent (children and adolescents), Research risks and benefits, Research trust and mistrust, Children, Parents, Clinical trials, Survey research, Health-care facilitiesUnited States, Qualitative (QL)

Kokolo, M. B., et al. (2011). HIV Pre-Exposure Prophylaxis (PrEP) – A Quantitative Ethics Appraisal. PLoS ONE 6(8): e22497.
Informed consent (adults), Investigator practices and perspectives, Research risks and benefits, Investigators, Research staff, Clinical trials, Health-care facilities,CanadaQuantitative (QT)

Lairumbi, G. M., Michael, P., Fitzpatrick, R., & English, M. C. (2012). Forms of benefit sharing in global health research undertaken in resource poor settings: A qualitative study of stakeholders views in Kenya. Philosophy, Ethics, and Humanities in Medicine, 7(7).
Research risks and benefits, Adults (other), Community Advisory Board, Investigators, IRB members, Policy makers, Clinical trials, Health-care facilities, South Africa, Qualitative (QL)

Länsimies‐Antikainen, H., Laitinen, T., Rauramaa, R., & Pietilä, A. M. (2010). Evaluation of informed consent in health research: a questionnaire survey. Scandinavian Journal of Caring Sciences, 24(1), 56-64.
Informed consent (adults), Adults (other), Clinical trials, Health-care facilities,FinlandQuantitative (QT)

Lazovski, J., Losso, M., Krohmal, B., Emanuel, E. Z., Grady, C., & Wendler, D. (2009). Benefits and burdens of participation in a longitudinal clinical trial. Journal of Empirical Research on Human Research Ethics, 4(3), 89-97.
Research risks and benefits, People living with HIV, Clinical trials, Health-care facilities, Argentina, Brazil, Thailand, Quantitative (QT)

Lindegger, G., Milford, C., Slack, C., Quayle, M., Xaba, X., & Vardas, E. (2006). Beyond the checklist: Assessing understanding for HIV vaccine trial participation in South Africa. Journal of Acquired Immune Deficiency Syndromes, 43, 560-566.
Informed consent (adults), People at risk for HIV, Clinical trials, Health-care facilities, South Africa, Mixed Methods (MM)

Lynöe, N., Sandlund, M., Dahlqvist, G., & Jacobsson, L. (1991). Informed consent: study of quality of information given to participants in a clinical trial. BMJ: British Medical Journal, 303(6803), 610-613.
Informed consent (adults), Voluntariness and self-efficacy, Adults with other health problems, Clinical trials, Health-care facilities, SwedenQuantitative (QT) 

Madhivanan, P., Krupp, K., Kulkarni, V., Kulkarni, S., Vaidya, N., Shaheen, R. Philpott, S. & Fisher, C. B. (2014). HIV testing among pregnant women living with HIV in India: are private healthcare providers routinely violating women’s human rights? BMC International Health and Human Rights, 14(7).
Confidentiality and privacy, Informed consent (adults), People living with HIV, Clinical trials, Community organizations, Health-care facilities, India, Qualitative (QL)

Meyers, K., Metzger, D. S., Navaline, H., Woody, G. E., & McLellan, A. T. (1994). HIV vaccine trials: Will intravenous drug users enroll? American Journal of Public Health, 84(5), 761-766.
Voluntariness and self-efficacyPeople at risk for HIV, People who inject drugs, Clinical trials, Health-care facilitiesUnited StatesQuantitative (QT)

Miller, C. K., O’Donnell, D. C., Searight, H. R., & Barbarash, R. A. (1996). The Deaconess Informed Consent Comprehension Test: an assessment tool for clinical research subjects. Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, 16(5), 872-878.
Informed consent (adults), Adults with other health problems, Clinical trials, Health-care facilities, United StatesQuantitative (QT)

Miller, V. A., Reynolds, W. W., Ittenbach, R. F., Luce, M. F., Beauchamp, T. L., & Nelson, R. M. (2009). Challenges in measuring a new construct: Perception of voluntariness for research and treatment decision making. Journal of empirical research on human research ethics: JERHRE, 4(3), 21-31.
Voluntariness and self-efficacy, Clinical Trials, Health-care facilities, United StatesQualitative (QL)

Miller, V. A., Reynolds, W. W., & Nelson, R. M. (2008). Parent–Child Roles in Decision Making About Medical Research. Ethics & Behavior, 18(2-3), 161-181.
Assent and self-consent (children and adolescents), Children, Parents, Clinical trials,Health-care facilities, United StatesMixed methods (MM)

Minniear, T. D., Gilmore, B., Arnold, S. R., Flynn, P. M., Knapp, K. M., & Gaur, A. H. (2009). Implementation of and barriers to routine HIV screening for adolescents. Pediatrics, 124, 1076-1083.
Assent and self-consent (children and adolescents), Adolescents, Health-care facilities, United States, Quantitative (QT)

Obermeyer, C., Verhulst, C., & Asmar, K. (2014). Could you have said no? A mixed-methods investigation of consent to HIV tests in four African countries. Journal Of The International AIDS Society, 1718898.
Informed consent (adults), Voluntariness and self-efficacy, People at risk for HIV, People at risk for or with other STIs, Survey research, Health-care facilities, South AfricaMixed Methods (MM)

Oliver, J. M., Slashinski, M. J., Wang, T., Kelly, P. A., Hilsenbeck, S. G., & McGuire, A. L. (2011). Balancing the risks and benefits of genomic data sharing: genome research participants’ perspectives. Public Health Genomics, 15(2), 106-114.
Confidentiality and privacy, Informed consent (adults), Research risks and benefits,Research trust and mistrust, Adults (other), Parents, Clinical trials, Health-care facilities, United StatesMixed methods (MM)

O’Lonergan, T. A., & Forster-Harwood, J. E. (2011). Novel approach to parental permission and child assent for research: Improving comprehension. Pediatrics, 127(5), 917-924.
Assent and self-consent (children and adolescents), Investigator practices and perspectives, Voluntariness and self-efficacy, Adolescents, Children, Ethics education,Multimedia, Survey research, Health-care facilities, United StatesQuantitative (QT)

Ott, M. A., Alexander, A. B., Lally, M., Steever, J. B., & Zimet, G. D. (2013). Preventive misconception and adolescents’ knowledge about HIV vaccine trials. Journal Of Medical Ethics: Journal Of The Institute Of Medical Ethics, 39(12), 765-771.
Assent and self-consent (children and adolescents), Therapeutic misconception,Adolescents, People at risk for HIV, People at risk for or with other STIs, Clinical trials,Health-care facilities, United StatesQualitative (QL)

Ott, M. A., Rosenberger, J. G., & Fortenberry, J. D. (2010). Parental permission and perceived research benefits in adolescent STI research.  Journal of empirical research on human research ethics: JERHRE, 5(2), 57-64.
Assent and self-consent (children and adolescents), Informed consent (adults), Research risks and benefits, Adolescents, Parents, People at risk for HIV, Clinical trials, Community organizations, Health-care facilities, United StatesQualitative (QL)

Palmer, B. W., Cassidy, E. L., Dunn, L. B., Spira, A. P., & Sheikh, J. I. (2008). Effective use of consent forms and interactive questions in the consent process. IRB: Ethics and Human Research, 30(2), 8-12.
Informed consent (adults), Voluntariness and self-efficacy, Adults with other health problems, Clinical trials, Health-care facilities, United StatesQualitative (QL)

Quirk, M. E., Godkin, M. A., & Schwenzfeier, E. (1993). Evaluation of two AIDS prevention interventions for inner-city adolescent and young adult women. American journal of preventive medicine.
Clinical efficacy, Adolescents, People at risk for HIV, People at risk for or with other STIs,Community-engaged research, Multimedia, Community organizations, Health-care facilitiesUnited StatesMixed methods (MM)

Rajabiun, S., Mallinson, R. K., McCoy, K., Coleman, S., Drainoni, M., Rebholz, C., & Holbert, T. (2007). Getting me back on track: The role of outreach interventions in engaging and retaining people living with HIV/AIDS in medical care. AIDS Patient Care and STDs, 21(Supp. 1), S20-S29.
Clinical efficacy, Voluntariness and self-efficacy, People living with HIV, Health-care facilities, United States, Qualitative (QL)

Rautenbach, C., Lindegger, G., Slack, C., Wallace, M., & Newman, P. (2015). I’m positive, but I’m negative: competing voices in informed consent and implications for HIV vaccine trials. Journal of Empirical Research on Human Research Ethics, 10 (2), 151-156.
Informed consent (adults)People living with HIVClinical trialsHealth-care facilitiesSouth AfricaQualitative (QL)

Reed, J. L., Thistlethwaite, J. M., & Huppert, J. S. (2007). STI research: Recruiting an unbiased sample. Journal of Adolescent Health, 41, 14-18.
Assent and self-consent (children and adolescents), Research risks and benefits, Adolescents, People at risk for HIV, People at risk for or with other STIs, Health-care facilities, United States, Quantitative (QT)

Roberts, L. W., Warner, T. D., Brody, J. L., Roberts, B., Lauriello, J., & Lyketsos,C. (2002). Patient and psychiatrist ratings of hypothetical schizophrenia research protocols: assessment of harm potential and factors influencing participation decisions. American Journal of Psychiatry, 159(4), 573-584.
Informed consent (adults), Adults (other), Adults with neurological disorders, Clinical trials,Health-care facilities, United StatesMixed methods (MM)

Roessler, B. J., Steneck, N. H., & Connally, L. (2015). The MICHR genomic DNA BioLibrary: an empirical study of the ethics of biorepository development. Journal of Empirical Research on Human Research Ethics, 10 (1), 37-48.
Informed consent (adults)Research risks and benefitsAdults (other)Health-care facilitiesUnited StatesQuantitative (QT) 

Rojas, N. L., Sherrit, L., Harris, S., & Knight, J. R. (2008). The role of parental consent in adolescent substance use research. Journal of Adolescent Health, 42, 192-197.
Assent and self-consent (children and adolescents), Adolescents, People at risk for or with substance use addictions, Clinical trials, Health-care facilities, United States, Quantitative (QT)

Rongkavilit, C., Naar-King, S., Chuenyam, T., Wang, B., Wright, K., & Phanuphak, P. (2007). Health risk behaviors among HIV-infected youth in Bangkok, Thailand. Journal of Adolescent Health, 40, 358e1-358e8.
Assent and self-consent (children and adolescents), Adolescents, People living with HIV, Health-care facilities, Thailand, Quantitative (QT)

Sahin, Y. S., Iyigun, E., & Acikel, C. (2014). Validity and reliability of a Turkish version of the Modified Moral Sensitivity Questionnaire for student nurses. Ethics and Behavior, 25 (4), 351-359.
Clinical efficacyCollege students and young adultsEthics education, Survey researchHealth-care facilities, Turkey, Quantitative (QT)

Shah, S., Whittle, A., Wilfond, B., Gensler, G., & Wendler, D. (2004). How do institutional review boards apply the federal risk and benefit standards for pediatric research?. JAMA: the journal of the American Medical Association,291(4), 476-482.
IRB practices and perspectives, Research risks and benefits, IRB members, Clinical trials,Survey research, Health-care facilities, United StatesQuantitative (QT)

Silaigwana, B., & Wassenaar, D. (2015). Biomedical research ethics committees in Sub-Saharan Africa: a collective review of their structure, functioning, and outcomes. Journal of Empirical Research on Human Research Ethics, 10 (2), 169-184.
IRB practices and perspectivesAdults (other)IRB membersClinical trialsEducational institutionsHealth-care facilitiesSouth AfricaMixed Methods (MM)

Simes, R. J., Tattersall, M. H., Coates, A., Raghavan, D., Solomon, H. J., & Smartt, H. (1986). Randomised comparison of procedures for obtaining informed consent in clinical trials of treatment for cancer. British medical journal (Clinical research ed.), 293(6554), 1065.
Informed consent (adults), Randomization, Adults with other health problems, Clinical trials,Health-care facilities, AustraliaQuantitative (QT)

Slomka, J., Ratliff, E. A., McCurdy, S. A., Timpson, S., & Williams, M.L. (2008). Decisions to participate in research: Views of underserved minority drug users with or at risk for HIV. AIDS Care, 20(10), 1224-1232.
Research risks and benefits, Voluntariness and self-efficacy, People at risk for HIV, People who inject drugs, Clinical trials, Health-care facilities, United States, Qualitative (QL)

Sugarman, J., Corneli, A., Donnell, D., Liu, T., Rose, S., Celentano, D., & … Metzger, D. (2011). Are there adverse consequences of quizzing during informed consent for HIV research?. Journal Of Medical Ethics, 37(11), 693-697.
Informed consent (adults), People at risk for HIV, People who inject drugs, Clinical trials,Health-care facilities, China, ThailandQuantitative (QT)

Thokoane, C. (2014). Ethical challenges for piloting sexual health programs for youth in Hammanskraal, South Africa: bridging the gap between rights and services. Ethics and Behavior, 25 (2), 169-179.
Assent and self-consent (children and adolescents), AdolescentsCommunity-engaged researchHealth-care facilitiesSouth Africa, Qualitative (QL)

Timmermans, S. & McKay,T. (2009). Clinical trials as treatment option: Bioethics and health care disparities in substance dependency. Social Science & Medicine, 69, 1784-1790.
Randomization, Therapeutic misconception, People at risk for or with substance use addictions, Clinical trials, Health-care facilities, United States, Qualitative (QL)

Willison, D. J., Keshavjee, K., Nair, K., Goldsmith, C., & Holbrook, A. M. (2003). Patients’ consent preferences for research uses of information in electronic medical records: interview and survey data. Bmj, 326(7385), 373.
Confidentiality and privacy, Informed consent (adults), Adult (other), Survey research,Health-care facilities, CanadaMixed methods (MM)

Wirshing, D. A., Wirshing, W. C., Marder, S. R., Liberman, R. P., & Mintz, J. (1998). Informed consent: assessment of comprehension. American Journal of Psychiatry, 155(11), 1508-1511.
Informed consent (adults), Adults with neurological disorders, Health-care facilities, United StatesQuantitative (QT)

Varas-Diaz, N., Negron, S. S., Neilands, T. B., Bou, F. C., & Rivera, S. M. (2010). Stigmatization of illicit drug use among Puerto Rican health professionals in training. Puerto Rico Health Sciences Journal, 29(2), 109-116.
Stigma, Adults (other), People at risk for or with substance use addictions, Health-care facilities, Puerto Rico, Mixed Methods (MM)

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