CASA: Community-based Accompaniment With Supervised Antiretrovirals in Lima, Peru

Sponsor
Brigham and Women's Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01070017
Collaborator
National Institute of Mental Health (NIMH) (NIH), Partners in Health (Other), Harvard School of Public Health (HSPH) (Other), Harvard Medical School (HMS and HSDM) (Other)
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Study Details

Study Description

Brief Summary

Using quantitative and qualitative data, this study will assess the impact of community accompaniment with supervised antiretrovirals (CASA) on HIV-positive individuals and community members in Lima, Peru.

Condition or Disease Intervention/Treatment Phase
  • Other: DOT-HAART
Phase 3

Detailed Description

Community-based accompaniment with directly observed antiretroviral therapy (DOT-HAART) may improve adherence and clinical outcomes among impoverished individuals starting HAART in resource-poor settings. Furthermore, the utilization of community health workers may build social capital. This is cluster-randomized trial, with randomization at the level of health centers. Individuals in both intervention and control clusters will receive community-based adherence support (monthly adherence visits) and standard care. In addition, individuals residing in intervention clusters will receive 12 months of community-based DOT-HAART. We will enroll patients as well as community members (health providers, treatment supporters, and community health workers) to assess individual and community-level outcomes.

Study Design

Study Type:
Interventional
Actual Enrollment :
1244 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Cluster randomization of sites assign individuals starting antiretroviral therapy to receive community-based directly observed therapy plus home visits / social support versus home visits / social support alone.Cluster randomization of sites assign individuals starting antiretroviral therapy to receive community-based directly observed therapy plus home visits / social support versus home visits / social support alone.
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Health Services Research
Official Title:
Community-based Accompaniment With Supervised Antiretrovirals in Lima, Peru
Study Start Date :
Feb 1, 2010
Actual Primary Completion Date :
Jul 31, 2012
Actual Study Completion Date :
Aug 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention: DOT-HAART

Intervention group will receive community-based monthly adherence visits, standard care, and DOT-HAART.

Other: DOT-HAART
For 8 months, DOT-HAART of all doses in the participant's home or alternate location. DOT worker ensures that HIV medications are taken as indicated and witnesses ingestion of all medications including other medications prescribed by physician. The worker will be trained to identify, triage and notify providers of any psychosocial and medical problems/complications. Transition to self-administration begins in months 9-12 when DOT will be tapered and greater participation of treatment supporter to prepare patients for self-administration.

No Intervention: No DOT-HAART

Control group receives community-based monthly adherence visits and standard care, but no DOT-HAART.

Outcome Measures

Primary Outcome Measures

  1. Proportion with suppressed HIV viral load after starting HAART among those receiving community-based DOT-HAART versus the control group. [18 and 24 months]

Secondary Outcome Measures

  1. Identify mediating mechanisms of CASA effect on individual outcomes. [24 months]

  2. Identify subgroups who respond best to CASA intervention. [24 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria for Patient Cohort:
  • Age greater than or equal to 18;

  • Diagnosis if HIV and meeting criteria for HAART;

  • Lives in poverty;

  • EITHER: 1) HAART naïve or 2) starting salvage therapy due to virologic failure;

  • Documentation of baseline CD4 cell count and HIV load;

  • Residence and receipt of HIV healthcare within the study catchment area

Exclusion Criteria for Patient Cohort:
  • Imprisoned or cannot give informed consent.
Inclusion Criteria for Community Cohort:
  • Working in a health establishments in study region;

  • If health personnel, contracted employee caring for people living with HIV/AIDS.

Exclusion Criteria for Community Cohort:
  • Cannot give informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Socios En Salud Lima Peru

Sponsors and Collaborators

  • Brigham and Women's Hospital
  • National Institute of Mental Health (NIMH)
  • Partners in Health
  • Harvard School of Public Health (HSPH)
  • Harvard Medical School (HMS and HSDM)

Investigators

  • Principal Investigator: Sonya Shin, MD, MPH, Brigham and Women's Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sonya Sunhi Shin, Dr., Brigham and Women's Hospital
ClinicalTrials.gov Identifier:
NCT01070017
Other Study ID Numbers:
  • 1R01MH083550-01A2
  • 1R01MH083550-01A2
First Posted:
Feb 17, 2010
Last Update Posted:
Oct 25, 2017
Last Verified:
Oct 1, 2017
Keywords provided by Sonya Sunhi Shin, Dr., Brigham and Women's Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 25, 2017