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Optimizing the Efficiency and Implementation of Cash Transfers to Improve Adherence to Antiretroviral Therapy

University of California (UC), Berkeley logo

University of California (UC), Berkeley

Status

Completed

Conditions

Adherence, Medication
Adherence, Patient
HIV/AIDS

Treatments

Behavioral: Active Arm 2
Behavioral: Active Arm 1

Study type

Interventional

Funder types

Other
Industry
NIH

Identifiers

NCT03351556
R01MH112432-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

  1. Determine the "dose-response" relationship between a cash transfer amount and HIV viral suppression at 6 months
  2. Identify the most effective cash transfer size to increase the proportion of people living with HIV infection (PLHIV) retained in care and with suppressed viral load (<1000 copies/ml) after 6 months. (This amount will be further evaluated in a cluster randomized trial in Phase 2).

Full description

Participants in the control group will receive the standard HIV primary care services according to Tanzania's National Guidelines for the Management of HIV and AIDS.

The study has two active intervention arms:

  1. The opportunity to earn 10,000 TZS/month (~$4.50) for up to 6 months conditional on visit attendance, and
  2. The opportunity to earn 22,500 TZS/month (~$10.00) for up to 6 months conditional on visit attendance

In both intervention arms, cash transfers will be delivered a maximum of once monthly, spaced ≥28 days apart, for up to six months and delivered via an automatic mobile money system linked to a biometric identification system.

Enrollment

530 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≥18 years
  • Living with HIV infection
  • Initiated antiretroviral therapy ≤1 month prior to enrollment in the study

Exclusion criteria

  • Participants who do no provide informed consent

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

530 participants in 3 patient groups

Comparison Arm
No Intervention group
Description:
Participants in the comparison group will receive the standard HIV primary care services according to Tanzania's National Guidelines for the Management of HIV and AIDS.
Active Intervention 1
Experimental group
Description:
Participants will receive the standard HIV primary care services according to Tanzania's National Guidelines for the Management of HIV and AIDS plus the opportunity to earn 10,000 TZS/month (\~$4.50) for up to 6 months conditional on visit attendance.
Treatment:
Behavioral: Active Arm 1
Active Intervention 2
Experimental group
Description:
Participants will receive the standard HIV primary care services according to Tanzania's National Guidelines for the Management of HIV and AIDS plus the opportunity to earn 22,500 TZS/month (\~$10.00) for up to 6 months conditional on visit attendance.
Treatment:
Behavioral: Active Arm 2

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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