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Clinical Trials/NCT01118767
NCT01118767CompletedNot Applicable

Evaluation of a Computer-Based System Using Cell Phones for HIV People in Peru

Universidad Peruana Cayetano Heredia2 sites in 1 country210 target enrollmentStarted: May 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
210
Locations
2
Primary Endpoint
Self-reported medication adherence

Study Overview

Brief Summary

The investigators propose to develop and evaluate a computer-based intervention using cell phones to enhance adherence to antiretroviral treatment (ART) and support of HIV transmission risk-reduction among adult HIV-positive patients in Peru.

Detailed Description

Adherence to ART is critical for treatment success at the individual level and to avoid the onset of resistant strains of HIV. In Peru, where ART has recently been introduced, adherence to HIV treatment has not yet been addressed properly. Innovative approaches using information technologies such as cell phones are needed to increase adherence to ART for people with HIV/AIDS. The specific aims of the study are to: 1) Conduct formative research to assess culturally-specific behavioral messages to be included in the computer-based system; 2) Develop and test an interactive computer-based system using cell phones to enhance adherence to ART and to deliver HIV transmission risk reduction messages; 3) Evaluate the impact of the system on antiretroviral adherence and sexual risk behaviors.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •HIV-positive healthy male or female aged greater than or equal to 18
  • •Currently on ART
  • •Patients with a mobile phone for their personal use (not shared)
  • •Patients who know how to retrieve read text messages on their mobile phone
  • •Signed and dated written informed consent prior to admission to the study

Exclusion Criteria

  • •Patients whose clinical condition might have interfered with the study (e.g., deafness, serious mental illness, mental retardation)
  • •Patients unable to give their informed consent.

Arms & Interventions

Cell phone intervention

Experimental

Participant receives short text messages

Intervention: Cell phone intervention (Other)

Standard of care

No Intervention

Participant receives standard of care support but not short text messages

Outcomes

Primary Outcomes

Self-reported medication adherence

Time Frame: 12 months

HIV-1 viral load

Time Frame: 12 months

Secondary Outcomes

  • CD4(12 months)
  • Self-reported HIV transmission risk behaviors(12 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Walter Curioso Vilchez

Universidad Peruana Cayetano Heredia

Universidad Peruana Cayetano Heredia

Study Sites (2)

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