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NCT Number: NCT05967208

Confidential Social Network Referrals for HIV Testing

Despite worldwide efforts to promote HIV testing, rates of testing remain low. The purpose of this study is to evaluate the acceptability, efficacy, and cost-effectiveness of confidential SMS-based social network referrals for HIV testing as a means of reaching high-risk individuals and prompting them to test for HIV. To accomplish this purpose, the study has 5 specific aims:

Aim 1 will conduct qualitative, formative work to identify desirable provider- and client-side characteristics of a confidential SMS-based HIV testing referral system.

Aim 2 will adapt an existing mHealth system (mParis) to add CONSORT functionality.

Aim 3 will pilot-test the CONSORT system to collect preliminary data on the system's acceptability, performance, and potential efficacy.

Aim 4 will evaluate the acceptability and efficacy of CONSORT in a randomized controlled trial.

Aim 5 will evaluate the incremental cost-effectiveness of CONSORT vs. other referral options.

If CONSORT is shown to be acceptable, effective, and cost-effective, such mobile-phone supported, chain-referral methods could greatly improve the cost-effectiveness of HIV testing efforts.

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Key information

Conditions

HIV

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

No additional detail available

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • at least 18 years old
  • live, work, or regularly receive care in Moshi, Tanzania
  • literate

Exclusion criteria

  • under age 18 years
  • does not live, work, or regularly receive care in Moshi, Tanzania
  • illiterate

Treatment and study plan

CONSORT referrals

Behavioral

Participants will be offered SMS-based confidential social network referrals for HIV testing ("CONSORT referrals") to extend to any of their social and sexual network contacts.

Card referrals

Behavioral

Participants will be offered physical invitation cards ("card referrals") to extend to any of their social and sexual network contacts.

Primary outcomes

  1. Uptake of HIV testing

    Time frame: Within 30 days of the time of the testing offer

    The number of referred clients presenting for HIV testing at participating study sites within 30 days of the testing offer, per 100 index clients.

Study contacts

Contact information is provided by the study sponsor or research team.

Jan Ostermann, PhD

CONTACT

[email protected]

+1-803-777-8747

Sponsors and collaborators

Lead sponsor

University of South Carolina

Other

Collaborators

  • Duke University
  • Kilimanjaro Christian Medical Centre, Tanzania

Registry information

Acronym: CONSORT

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Aug 1, 2023
Registry last updated
Aug 1, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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