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N/A N=100 Randomized Supportive Care

Estamos Juntos (We Are Together): Improving HIV Care Delivery by Capacitating Health Care Providers

Hiv

Enrolled (actual)
100
Serious AEs
0.0%
Results posted
Sep 2025
Primary outcome: Primary: Burnout — -2.0; -5.9; -5.3; -3.9 units on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
behavioral therapy and education (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Vanderbilt University Medical Center
Primary completion
Feb 2025

Outcome Measures

OutcomeResultp-value
PRIMARY
Burnout
-2.0; -5.9; -5.3; -3.9

Summary

Health care workers' negative behavior towards patients (likely a reflection of low job satisfaction, frustration with delivering HIV care and treatment in extremely resource-limited settings, and burnout) is one of the primary reasons people living with HIV abandon treatment in Mozambique. The purpose of this proposal is to test the impact and implementation of a provider resilience intervention and an anti-stigma intervention, individually and in combination, using a randomized controlled trial design at four health facilities. This potentially high-impact intervention offers the opportunity to test a low-cost, provider-focused approach to improving HIV treatment that, if proven effective at increasing adherence and retention in care, could be tested in a fully powered R01 trial in Mozambique.

Eligibility Criteria

Provider Criteria

Inclusion Criteria

  • Adult individuals, 18 years of age or older;
  • working as physicians, nurses, medical technicians, health counselors, community health care workers, or other clinical and non-clinical staff (e.g., receptionists, data entry clerk) who provide health services to adults living with HIV at one of the four study sites;
  • willing to be followed as a study participant during the 6-month study period, and does not intend to transfer to another health facility (HF) during the study period (per investigator's assessment at time of recruitment), as self-reported.
  • Be able to read and write in Portuguese, as self-reported.

Exclusion Criteria

  • Those who are not permanent members of the health facility staff (i.e., floating providers that work at multiple sites in a given week);
  • Any clinical or mental condition, including the influence of drugs or alcohol at the time of study recruitment, that as per the investigator's opinion/assessment, would preclude the provision of informed consent or make study participation unsafe or unethical;
  • Individuals working in the health facility but from the following cadres: drivers, security personnel, and workers with no patient-facing roles.

Patient Criteria

Inclusion:

  • Adult individuals, 18 years of age or older
  • Active in care (i.e., not in default)
  • Receiving HIV care and treatment at one of the four study sites.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05938621). 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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