Personal and community benefits and harms of research : views from Rakai, Uganda
To assess what individuals in low-income countries perceive as benefits and harms of population-based HIV/STD research. A total of 811 research participants, research decliners, and community opinion leaders in the Rakai District, Uganda were surveyed. Types of personal and community benefits and ha...
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Veröffentlicht in: | AIDS (London) 2007-11, Vol.21 (18), p.2493-2501 |
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creator | THIESSEN, Carrie SSEKUBUGU, Robert WAGMAN, Jennifer KIDDUGAVU, Mohammed WAWER, Maria J EMANUEL, Ezekiel GRAY, Ronald SERWADDA, David GRADY, Christine |
description | To assess what individuals in low-income countries perceive as benefits and harms of population-based HIV/STD research.
A total of 811 research participants, research decliners, and community opinion leaders in the Rakai District, Uganda were surveyed. Types of personal and community benefits and harms, as well as rates of reporting great personal and community benefit were assessed.
Using logistic regression, demographic characteristics, participant and opinion leader status, use of Rakai Health Sciences Program (RHSP) services, and perceived research effects were entered as predictors of reported great personal and great community benefit.
Most respondents thought that RHSP research was of great personal (85%) and community (88%) benefit. The perception that the RHSP was a great personal benefit was correlated with female sex, post-secondary education, frequent use of RHSP-sponsored medical services, health knowledge gains, and increased hope for future health improvements. Persons of non-Baganda ethnicity and 30-39 year-olds were less likely to believe research was personally beneficial. Regarding research as a great community benefit was associated with reported health knowledge gains, greater hope for Rakai residents' future health, and local economic benefit. Decliners were the most likely to report a personal harm, while community opinion leaders identified community harms at the highest rates.
The majority of Rakai residents report that HIV/STD research has enhanced their own and their communities' welfare. Different factors were associated with the belief that research is a personal versus community benefit. Variations in participant, decliner, and community opinion leader perceptions highlight inadequacies of current community consultation mechanisms. |
doi_str_mv | 10.1097/QAD.0b013e3282f029d3 |
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A total of 811 research participants, research decliners, and community opinion leaders in the Rakai District, Uganda were surveyed. Types of personal and community benefits and harms, as well as rates of reporting great personal and community benefit were assessed.
Using logistic regression, demographic characteristics, participant and opinion leader status, use of Rakai Health Sciences Program (RHSP) services, and perceived research effects were entered as predictors of reported great personal and great community benefit.
Most respondents thought that RHSP research was of great personal (85%) and community (88%) benefit. The perception that the RHSP was a great personal benefit was correlated with female sex, post-secondary education, frequent use of RHSP-sponsored medical services, health knowledge gains, and increased hope for future health improvements. Persons of non-Baganda ethnicity and 30-39 year-olds were less likely to believe research was personally beneficial. Regarding research as a great community benefit was associated with reported health knowledge gains, greater hope for Rakai residents' future health, and local economic benefit. Decliners were the most likely to report a personal harm, while community opinion leaders identified community harms at the highest rates.
The majority of Rakai residents report that HIV/STD research has enhanced their own and their communities' welfare. Different factors were associated with the belief that research is a personal versus community benefit. Variations in participant, decliner, and community opinion leader perceptions highlight inadequacies of current community consultation mechanisms.</description><identifier>ISSN: 0269-9370</identifier><identifier>EISSN: 1473-5571</identifier><identifier>DOI: 10.1097/QAD.0b013e3282f029d3</identifier><identifier>PMID: 18025886</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adult ; AIDS/HIV ; Attitude to Health ; Biological and medical sciences ; Developing Countries ; Ethics, Research ; Female ; Health Knowledge, Attitudes, Practice ; HIV Infections - psychology ; HIV Infections - therapy ; Human immunodeficiency virus ; Human viral diseases ; Humans ; Infectious diseases ; Male ; Medical sciences ; Refusal to Participate - psychology ; Research Subjects - psychology ; Risk Assessment ; Sexually Transmitted Diseases - psychology ; Socioeconomic Factors ; Therapeutic Human Experimentation - ethics ; Uganda ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids</subject><ispartof>AIDS (London), 2007-11, Vol.21 (18), p.2493-2501</ispartof><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-11e9bea99f3f27f0262c9007147abe0b5f9a44f0aa298e2ad15d7fb6f680dd693</citedby><cites>FETCH-LOGICAL-c412t-11e9bea99f3f27f0262c9007147abe0b5f9a44f0aa298e2ad15d7fb6f680dd693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19942183$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18025886$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>THIESSEN, Carrie</creatorcontrib><creatorcontrib>SSEKUBUGU, Robert</creatorcontrib><creatorcontrib>WAGMAN, Jennifer</creatorcontrib><creatorcontrib>KIDDUGAVU, Mohammed</creatorcontrib><creatorcontrib>WAWER, Maria J</creatorcontrib><creatorcontrib>EMANUEL, Ezekiel</creatorcontrib><creatorcontrib>GRAY, Ronald</creatorcontrib><creatorcontrib>SERWADDA, David</creatorcontrib><creatorcontrib>GRADY, Christine</creatorcontrib><title>Personal and community benefits and harms of research : views from Rakai, Uganda</title><title>AIDS (London)</title><addtitle>AIDS</addtitle><description>To assess what individuals in low-income countries perceive as benefits and harms of population-based HIV/STD research.
A total of 811 research participants, research decliners, and community opinion leaders in the Rakai District, Uganda were surveyed. Types of personal and community benefits and harms, as well as rates of reporting great personal and community benefit were assessed.
Using logistic regression, demographic characteristics, participant and opinion leader status, use of Rakai Health Sciences Program (RHSP) services, and perceived research effects were entered as predictors of reported great personal and great community benefit.
Most respondents thought that RHSP research was of great personal (85%) and community (88%) benefit. The perception that the RHSP was a great personal benefit was correlated with female sex, post-secondary education, frequent use of RHSP-sponsored medical services, health knowledge gains, and increased hope for future health improvements. Persons of non-Baganda ethnicity and 30-39 year-olds were less likely to believe research was personally beneficial. Regarding research as a great community benefit was associated with reported health knowledge gains, greater hope for Rakai residents' future health, and local economic benefit. Decliners were the most likely to report a personal harm, while community opinion leaders identified community harms at the highest rates.
The majority of Rakai residents report that HIV/STD research has enhanced their own and their communities' welfare. Different factors were associated with the belief that research is a personal versus community benefit. Variations in participant, decliner, and community opinion leader perceptions highlight inadequacies of current community consultation mechanisms.</description><subject>Adult</subject><subject>AIDS/HIV</subject><subject>Attitude to Health</subject><subject>Biological and medical sciences</subject><subject>Developing Countries</subject><subject>Ethics, Research</subject><subject>Female</subject><subject>Health Knowledge, Attitudes, Practice</subject><subject>HIV Infections - psychology</subject><subject>HIV Infections - therapy</subject><subject>Human immunodeficiency virus</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Refusal to Participate - psychology</subject><subject>Research Subjects - psychology</subject><subject>Risk Assessment</subject><subject>Sexually Transmitted Diseases - psychology</subject><subject>Socioeconomic Factors</subject><subject>Therapeutic Human Experimentation - ethics</subject><subject>Uganda</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><issn>0269-9370</issn><issn>1473-5571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLAzEUhYMotj7-gUg2unL0JpnMJO5KfULBB3Y93Jm5saPzqEmr-O8dtVBw4-rC5TuHw8fYgYBTATY9exhdnEIOQpGSRjqQtlQbbCjiVEVap2KTDUEmNrIqhQHbCeEFADQYs80GwoDUxiRDdn9PPnQt1hzbkhdd0yzbavHJc2rJVYvw856hbwLvHPcUCH0x4-f8vaKPwJ3vGv6Ir1id8Olzz-Ie23JYB9pf3V02vbp8Gt9Ek7vr2_FoEhWxkItICLI5obVOOZn26xNZWIC0n485Qa6dxTh2gCitIYml0GXq8sQlBsoysWqXHf_2zn33tqSwyJoqFFTX2FK3DFlitBRaqn9BKUAnvZYejH_BwncheHLZ3FcN-s9MQPatPOuVZ3-V97HDVf8yb6hch1aOe-BoBWAosHYe26IKa87aWAqj1Bc6TonT</recordid><startdate>20071130</startdate><enddate>20071130</enddate><creator>THIESSEN, Carrie</creator><creator>SSEKUBUGU, Robert</creator><creator>WAGMAN, Jennifer</creator><creator>KIDDUGAVU, Mohammed</creator><creator>WAWER, Maria J</creator><creator>EMANUEL, Ezekiel</creator><creator>GRAY, Ronald</creator><creator>SERWADDA, David</creator><creator>GRADY, Christine</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20071130</creationdate><title>Personal and community benefits and harms of research : views from Rakai, Uganda</title><author>THIESSEN, Carrie ; SSEKUBUGU, Robert ; WAGMAN, Jennifer ; KIDDUGAVU, Mohammed ; WAWER, Maria J ; EMANUEL, Ezekiel ; GRAY, Ronald ; SERWADDA, David ; GRADY, Christine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-11e9bea99f3f27f0262c9007147abe0b5f9a44f0aa298e2ad15d7fb6f680dd693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>AIDS/HIV</topic><topic>Attitude to Health</topic><topic>Biological and medical sciences</topic><topic>Developing Countries</topic><topic>Ethics, Research</topic><topic>Female</topic><topic>Health Knowledge, Attitudes, Practice</topic><topic>HIV Infections - psychology</topic><topic>HIV Infections - therapy</topic><topic>Human immunodeficiency virus</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Refusal to Participate - psychology</topic><topic>Research Subjects - psychology</topic><topic>Risk Assessment</topic><topic>Sexually Transmitted Diseases - psychology</topic><topic>Socioeconomic Factors</topic><topic>Therapeutic Human Experimentation - ethics</topic><topic>Uganda</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>THIESSEN, Carrie</creatorcontrib><creatorcontrib>SSEKUBUGU, Robert</creatorcontrib><creatorcontrib>WAGMAN, Jennifer</creatorcontrib><creatorcontrib>KIDDUGAVU, Mohammed</creatorcontrib><creatorcontrib>WAWER, Maria J</creatorcontrib><creatorcontrib>EMANUEL, Ezekiel</creatorcontrib><creatorcontrib>GRAY, Ronald</creatorcontrib><creatorcontrib>SERWADDA, David</creatorcontrib><creatorcontrib>GRADY, Christine</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>AIDS (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>THIESSEN, Carrie</au><au>SSEKUBUGU, Robert</au><au>WAGMAN, Jennifer</au><au>KIDDUGAVU, Mohammed</au><au>WAWER, Maria J</au><au>EMANUEL, Ezekiel</au><au>GRAY, Ronald</au><au>SERWADDA, David</au><au>GRADY, Christine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Personal and community benefits and harms of research : views from Rakai, Uganda</atitle><jtitle>AIDS (London)</jtitle><addtitle>AIDS</addtitle><date>2007-11-30</date><risdate>2007</risdate><volume>21</volume><issue>18</issue><spage>2493</spage><epage>2501</epage><pages>2493-2501</pages><issn>0269-9370</issn><eissn>1473-5571</eissn><abstract>To assess what individuals in low-income countries perceive as benefits and harms of population-based HIV/STD research.
A total of 811 research participants, research decliners, and community opinion leaders in the Rakai District, Uganda were surveyed. Types of personal and community benefits and harms, as well as rates of reporting great personal and community benefit were assessed.
Using logistic regression, demographic characteristics, participant and opinion leader status, use of Rakai Health Sciences Program (RHSP) services, and perceived research effects were entered as predictors of reported great personal and great community benefit.
Most respondents thought that RHSP research was of great personal (85%) and community (88%) benefit. The perception that the RHSP was a great personal benefit was correlated with female sex, post-secondary education, frequent use of RHSP-sponsored medical services, health knowledge gains, and increased hope for future health improvements. Persons of non-Baganda ethnicity and 30-39 year-olds were less likely to believe research was personally beneficial. Regarding research as a great community benefit was associated with reported health knowledge gains, greater hope for Rakai residents' future health, and local economic benefit. Decliners were the most likely to report a personal harm, while community opinion leaders identified community harms at the highest rates.
The majority of Rakai residents report that HIV/STD research has enhanced their own and their communities' welfare. Different factors were associated with the belief that research is a personal versus community benefit. Variations in participant, decliner, and community opinion leader perceptions highlight inadequacies of current community consultation mechanisms.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>18025886</pmid><doi>10.1097/QAD.0b013e3282f029d3</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Complete |
subjects | Adult AIDS/HIV Attitude to Health Biological and medical sciences Developing Countries Ethics, Research Female Health Knowledge, Attitudes, Practice HIV Infections - psychology HIV Infections - therapy Human immunodeficiency virus Human viral diseases Humans Infectious diseases Male Medical sciences Refusal to Participate - psychology Research Subjects - psychology Risk Assessment Sexually Transmitted Diseases - psychology Socioeconomic Factors Therapeutic Human Experimentation - ethics Uganda Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids |
title | Personal and community benefits and harms of research : views from Rakai, Uganda |
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