Examining the effectiveness of an intervention to reduce HIV-related self-stigma in PLHIV

Completed

• Conditions: hiv stigma en psychosociale gezondheid; hiv gerelateerd stigma

• Registration Number: NL-OMON49731
• Lead Sponsor: Open Universiteit

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 9 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 160

Inclusion Criteria

a) having a diagnosis of HIV; b) being 18 years or older; c) being enrolled in
HIV care in the Netherlands; d) able to speak Dutch or English.

Exclusion Criteria

Subjects with a serious medical, psychiatric or cognitive disease that would
interfere with participation (e.g. severe clinical depression with risk of
suicide or people with a serious drug or alcohol problem).

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Primary outcomes of the RCT are the Berger HIV Stigma Scale (HSS), the World<br /><br>Health Organization Quality of Life questionnaire (WHOQOL-BREF), the Rosenberg<br /><br>Self Esteem Scale (RSES), the Empowerment Scale Rogers (ESR), and the Brief<br /><br>Resilient Coping Scale (BRCS). The HSS, WHOQOL-BREF, RSES, ESR, BRCS will be<br /><br>administered at baseline, post intervention and at three-month (post<br /><br>intervention) follow up. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>-</p><br>