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N/A N=76 Randomized Prevention

A Pilot Intervention to Improve Coping With Discrimination and Adherence Among HIV-Positive Latino MSM

HIV

Enrolled (actual)
76
Serious AEs
0.0%
Results posted
Feb 2021
Primary outcome: Primary: Continuous Adherence (MEMS) — 86.7; 79.0; 85.5; 79.7 % of doses taken, past month — p=0.06

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Siempre Seguiré (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
Male
Sponsor
RAND
Primary completion
Sep 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Continuous Adherence (MEMS)
86.7; 79.0; 85.5; 79.7 0.06
PRIMARY
Continuous Adherence (Self-report)
97.48; 94.57; 99.17; 92.91 0.02 sig
SECONDARY
Functional Coping Strategies
2.75; 2.68; 2.82; 2.74 0.39
SECONDARY
Positive Religious Coping Strategies
1.84; 2.08; 1.72; 2.08 0.54
SECONDARY
Dysfunctional Coping Strategies
2.05; 2.09; 2.06; 2.09 0.81
SECONDARY
Negative Religious Coping Strategies
0.17; 0.34; 0.22; 0.30 0.06
SECONDARY
Medical Mistrust (General)
2.34; 2.78; 2.28; 2.88 0.16
SECONDARY
Medical Mistrust (HIV Conspiracy Beliefs)
1.81; 2.26; 1.90; 2.40 0.02 sig
SECONDARY
Internalized Stigma (Sexual Orientation)
1.53; 1.59; 1.68; 1.59 0.71
SECONDARY
Internalized Stigma (HIV)
2.38; 2.38; 2.14; 2.65 0.10

Summary

R34-funded study to pilot test an intervention to improve coping with discrimination and adherence among Latino men who have sex with men (MSM) living with HIV. The proposed research aims to modify and refine Siempre Seguiré, a culturally congruent cognitive behavior therapy group intervention for HIV-positive Latino men who have sex with men (LMSM), to include strategies for ART adherence and retention in HIV care; and to conduct a small randomized pilot of Siempre Seguiré to examine feasibility and acceptability, as well as to explore preliminary effects on coping responses to discrimination and antiretroviral treatment adherence among LMSM living with HIV.

Eligibility Criteria

Inclusion Criteria

  • Age 18 years-old or older, HIV-positive, biologically male at birth and continue to identify as male, identify as Latino, report having sex with men in the past 12 months, and prescribed ART.

Exclusion Criteria

  • Being unwilling or unable to provide informed consent; having mental health problems that require immediate treatment (e.g., psychotic symptoms) or a diagnosed mental disorder that would limit ability to participate (e.g., dementia); and cognitive impairments that result in limited ability to provide informed consent.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03432819). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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