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Supporting peer researchers: recommendations from our lived experience/expertise in community-based research in Canada
by
Watson, James R.
, Tavares, James
, Ibáñez-Carrasco, Francisco
in
Acquired immune deficiency syndrome
/ Advocacy
/ AIDS
/ Best practices
/ Best practices for support
/ Commentary
/ Community action
/ Community-based research
/ Compensation
/ Disclosure of information
/ Emotions
/ Handicapped accessibility
/ Harm reduction
/ Health Promotion and Disease Prevention
/ Health Psychology
/ HIV
/ HIV patients
/ Human immunodeficiency virus
/ Lived experience of HIV
/ Management
/ Medicine
/ Medicine & Public Health
/ Peer researchers
/ Peer review
/ Peers
/ Public awareness
/ Public health
/ Researchers
/ Role models
/ Sexually transmitted disease research
/ Social aspects
/ Social Policy
/ Social Work
/ Stigma
/ The Involvement and Engagement of Peers in Research
2019
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Supporting peer researchers: recommendations from our lived experience/expertise in community-based research in Canada
by
Watson, James R.
, Tavares, James
, Ibáñez-Carrasco, Francisco
in
Acquired immune deficiency syndrome
/ Advocacy
/ AIDS
/ Best practices
/ Best practices for support
/ Commentary
/ Community action
/ Community-based research
/ Compensation
/ Disclosure of information
/ Emotions
/ Handicapped accessibility
/ Harm reduction
/ Health Promotion and Disease Prevention
/ Health Psychology
/ HIV
/ HIV patients
/ Human immunodeficiency virus
/ Lived experience of HIV
/ Management
/ Medicine
/ Medicine & Public Health
/ Peer researchers
/ Peer review
/ Peers
/ Public awareness
/ Public health
/ Researchers
/ Role models
/ Sexually transmitted disease research
/ Social aspects
/ Social Policy
/ Social Work
/ Stigma
/ The Involvement and Engagement of Peers in Research
2019
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Do you wish to request the book?
Supporting peer researchers: recommendations from our lived experience/expertise in community-based research in Canada
by
Watson, James R.
, Tavares, James
, Ibáñez-Carrasco, Francisco
in
Acquired immune deficiency syndrome
/ Advocacy
/ AIDS
/ Best practices
/ Best practices for support
/ Commentary
/ Community action
/ Community-based research
/ Compensation
/ Disclosure of information
/ Emotions
/ Handicapped accessibility
/ Harm reduction
/ Health Promotion and Disease Prevention
/ Health Psychology
/ HIV
/ HIV patients
/ Human immunodeficiency virus
/ Lived experience of HIV
/ Management
/ Medicine
/ Medicine & Public Health
/ Peer researchers
/ Peer review
/ Peers
/ Public awareness
/ Public health
/ Researchers
/ Role models
/ Sexually transmitted disease research
/ Social aspects
/ Social Policy
/ Social Work
/ Stigma
/ The Involvement and Engagement of Peers in Research
2019
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Supporting peer researchers: recommendations from our lived experience/expertise in community-based research in Canada
Journal Article
Supporting peer researchers: recommendations from our lived experience/expertise in community-based research in Canada
2019
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Overview
Community-based research in HIV in Canada is a complex undertaking. Including peer researchers living with HIV meaningfully is intricate and costly. However, this inclusion guarantees results that translate to community action, policy-making, and public awareness. Including HIV+ peer researchers expedites the path from research to intervention. However, we must constantly review our support in light of three implicit tasks performed by peer researchers: constant disclosure, emotional labor, and advocating for meaningful participation. Our team offers four pillars of support to reduce harm and strengthen the self-determination, confidence, advocacy, and impact for HIV+ peer researchers. The provision of emotional, instrumental, educational, and cultural/spiritual support might seldom be standardized within a study, but to successfully engage in community-based research, study teams must articulate what support can be offered in each area.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
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