Strengthening Families Living With HIV in Kenya

Sponsor
The University of Texas Medical Branch, Galveston (Other)
Overall Status
Recruiting
CT.gov ID
NCT04588883
Collaborator
(none)
810
1
1
40.9
19.8

Study Details

Study Description

Brief Summary

This study seeks to use a group-based microfinance/internal lending model to develop social capital among people with HIV in Kenya. This will create a context to deliver validated curriculum targeting intimate partner violence, positive parenting, agriculture, small business entrepreneurship, group-interpersonal therapy, and other determinants of well-being and ART adherence among people with HIV. The primary outcomes are viral suppression, ART adherence, and common mental disorders.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Kuja Pamoja - HIV
N/A

Detailed Description

It is anticipated that involvement in an internal savings and lending program will create social capital among people with HIV and their guardians (in case of adolescents w HIV). This social capital accrual will be leveraged to support and disseminate social skills (i.e. positive parenting, conflict resolution), economic skills (i.e. entrepreneurship, farming), and health skills (i.e. ART adherence, retention in care to produce viral suppression). The overall outcome is improved social, health, and economic well-being.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
810 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Strengthening Families Living With HIV in Kenya
Actual Study Start Date :
Sep 28, 2021
Anticipated Primary Completion Date :
Feb 25, 2025
Anticipated Study Completion Date :
Feb 25, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Arm

Patients, adults and adolescents, will be recruited from patient registries at 7 government operated HIV clinics in Meru County, Kenya. Patients will complete validated questionnaires at baseline, 1.5 year and 3 years into a novel adaptation of a community empowerment program. The program utilizes savings- and internal-lending/group-based microfinance process to facilitate exchange of savings amongst patients and adolescent guardians. A byproduct of this process is the development of social capital, which will be used to facilitate education, peer learning, and collective problem solving to improve determinants of well-being and clinical adherence among participants. Expected outcomes include improved viral suppression, ART adherence, clinical attendance, and mental health.

Behavioral: Kuja Pamoja - HIV
Information has been provided in the treatment arm description.

Outcome Measures

Primary Outcome Measures

  1. Viral Suppression [Change from baseline to 3 years]

    Viral suppression is measured as an undetectable viral load using standard clinic procedures.

  2. Anti-retroviral therapy Adherence [Change from baseline to 3 years]

    Anti-retroviral therapy (ART) adherence will be measured by patient report using the adherence portions of the AIDS Clinical Trial Group (ACTG) Adherence tool and by refill history.

  3. Depression [Change from baseline to 3 years]

    Depression will be measured using the Beck's Depression Inventory. Higher scores mean more depressive symptoms present.

  4. Anxiety [Change from baseline to 3 years]

    Anxiety will be measured using the Generalized Anxiety Disorder (GAD7) instrument. Higher score means more anxiety symptoms present.

  5. Post-Traumatic Stress Disorder [Change from baseline to 3 years]

    Post-traumatic stress disorder (PTSD) will be measured using the PTSD symptom scale. Higher scores mean more PTSD symptoms present.

Secondary Outcome Measures

  1. Group entitativity [Change from baseline to 3 years]

    Social cohesion (operationalized as group entitativity) will be measured using the Generalized Entitativity Measure (GEM). Higher score on this visual analogue scale means higher group entitativity.

  2. Intimate partner violence [Change from baseline to 3 years]

    Family violence will be measured using the Conflict Tactics Scale (CTS-2). Higher scale scores mean more conflict present; higher violence/coercive subscale scores mean more violence and coercion present.

  3. Food insecurity [Change from baseline to 3 years]

    Food security will be measured using the Household Food Insecurity Scale instrument. Higher scale scores mean higher food insecurity.

  4. Social trust [Change from baseline to 3 years]

    Social trust will be measured using a single validated item. This is a binary outcome with 1=presence of trust between respondent and other similar aged people with HIV.

  5. Expectations of mutual support [Change from baseline to 3 years.]

    Expectation of mutual support will be measured using the a single validated item. Higher score means higher expectation of mutual support between respondent and other similar-aged people with HIV.

  6. Child-guardian conflict [Change from baseline to 3 years.]

    Child-guardian conflict will be measured using the Conflict Tactics Scale for children (CTS2-pc). Higher scale score means more conflict present; higher violence subscale scores mean more violent conflicts used.

Eligibility Criteria

Criteria

Ages Eligible for Study:
13 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
Criteria for inclusion of subjects include:
  • testing positive for HIV, confirmed by the Ministry of Health clinics

  • being at or older than 13 years of age

  • initiating care at a qualified Ministry of Health clinic in the catchment area, or intending to initiate care at such a clinic (see below for definition)

  • Any gender, age (13+ years), and comorbid disease states

  • Provide informed consent if adult, emancipated minor or mature minor

  • Provide assent if minor with guardian, who must provide informed consent

Qualified clinical locations include

  • those with accessible and usable public land to convene weekly meetings,

  • no current program targeting families with HIV known to the Ministry of Health

Exclusion Criteria:
  • Refusal to participate

  • Current participation in a similar program

  • Residing in a location with a similar program targeting patients with HIV

  • Not covered by inclusion criteria.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Meru County Department of Health Maua Meru County Kenya

Sponsors and Collaborators

  • The University of Texas Medical Branch, Galveston

Investigators

  • Principal Investigator: Michael L Goodman, DrPH, The University of Texas Medical Branch, Galveston
  • Study Director: Stanley Gitari, MPH, Sodzo Kenya

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
The University of Texas Medical Branch, Galveston
ClinicalTrials.gov Identifier:
NCT04588883
Other Study ID Numbers:
  • 19-0241
First Posted:
Oct 19, 2020
Last Update Posted:
Sep 29, 2021
Last Verified:
Jul 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 29, 2021