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Efficacy and implementation potential of an online CBT-based counseling program for HIV-positive MSM patients: A randomized controlled trial of iESTEEM

Efficacy and implementation potential of an online CBT-based counseling program for HIV-positive MSM patients: A randomized controlled trial of iESTEEM

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080263
Enrollment
Unknown
Registered
2024-01-24
Start date
2024-07-29
Completion date
Unknown
Last updated
2025-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV/AIDS

Interventions

Intervention group:an online CBT-based counseling program (iESTEEM program)
weekly monitoring
Control group:weekly monitoring

Sponsors

Xiangya School of Nursing Central South University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 53 Years

Inclusion criteria

Inclusion criteria: 1) be 18 years old or above; 2) report having sex with men in their lifetime; 3) be diagnosed with HIV; 4) have started ART for at least one month; 5) report anxiety and/or depression symptoms (score of 5 to 14 on the Chinese-validated GAD-7 or the Chinese-validated PHQ-9); 6) not using mental health services in past 3 months (>2 visits/mo); 7) last month’s ART adherence < 95%; 8) frequently using WeChat in smartphone.

Exclusion criteria

Exclusion criteria: Participants who exhibit active mania, psychosis, or suicidality, as assessed by the SCID-Psych Screen, or are hospitalized will be excluded and referred to local mental health services.

Design outcomes

Primary

MeasureTime frame
Depression;Anxiety;Quality of life;Medication adherence;

Secondary

MeasureTime frame
Sexual orientation concealment;Internalized homophobia;HIV stigma;HIV related stress;HIV social support;CD4 counts;VL;

Countries

China

Contacts

Public ContactXianhong Li

Xiangya School of Nursing Central South University

xianhong_li@csu.edu.cn+86 135 0848 9466

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026