Participant Rights and Protections in Non-Profit Research: Safeguarding Welfare, Vulnerable Groups, and Community Engagement

Protecting participant rights is a cornerstone of ethical non-profit research, particularly when engaging with vulnerable and marginalized communities. This article examines strategies for safeguarding welfare through risk assessments, confidentiality agreements, and ongoing monitoring, while highlighting protections for children, elderly participants, and marginalized groups. It also explores mechanisms for addressing participant concerns and stresses the importance of cultural sensitivity and inclusivity. Beyond safeguarding, the article emphasizes community empowerment through advisory boards, active involvement, and co-ownership of research outcomes. By linking international ethical principles with practical strategies, it provides a roadmap for ensuring participant dignity, accountability, and trust-based research relationships.

Authors

Publication Details

Published
2025-01-01
DOI
https://doi.org/10.64357/neya-gjnps-rsc-eth-dt-07
Citations
2
Primary Topic
Ethics in Clinical Research
Type
article
Field-Weighted Citation Impact
3.76
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article

Participant Rights and Protections in Non-Profit Research: Safeguarding Welfare, Vulnerable Groups, and Community Engagement

Anna Neya Kazanskaia
2 citations
Ethics in Clinical Research
3.76
article

Participant Rights and Protections in Non-Profit Research: Safeguarding Welfare, Vulnerable Groups, and Community Engagement

Anna Neya Kazanskaia
article en
2 citations

Abstract

Protecting participant rights is a cornerstone of ethical non-profit research, particularly when engaging with vulnerable and marginalized communities. This article examines strategies for safeguarding welfare through risk assessments, confidentiality agreements, and ongoing monitoring, while highlighting protections for children, elderly participants, and marginalized groups. It also explores mechanisms for addressing participant concerns and stresses the importance of cultural sensitivity and inclusivity. Beyond safeguarding, the article emphasizes community empowerment through advisory boards, active involvement, and co-ownership of research outcomes. By linking international ethical principles with practical strategies, it provides a roadmap for ensuring participant dignity, accountability, and trust-based research relationships.

Openalex Percentile: Top 6%
Ethics in Clinical Research
3.76
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