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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02139176
Other study ID # 13-3707
Secondary ID
Status Recruiting
Phase N/A
First received May 13, 2014
Last updated November 14, 2014
Start date March 2014
Est. completion date January 2015

Study information

Verified date November 2014
Source University of North Carolina, Chapel Hill
Contact Nora E Rosenberg, PhD
Phone +265 (0)99 109 0676
Email Nora_Rosenberg@unc.edu
Is FDA regulated No
Health authority Malawi: National Health Sciences Research CommitteeUnited States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

In sub-Saharan Africa, engaging men in HIV prevention, care, and treatment has proven challenging. Along all steps of the HIV care-seeking cascade, men exhibit worse care-seeking behaviors than women. They are less likely to be tested for HIV, initiate combination antiretroviral therapy (cART), and be retained in cART care. Additionally, men rarely engage in the care of their female sex partners, even though couple care-seeking is associated with marked improvements in condom use within HIV-discordant couples. Option B+, Malawi's program for providing immediate, lifelong combination antiretroviral therapy (cART) to all HIV-infected pregnant women at the time of diagnosis, is an important entry-point for involving male partners in care.

This is a pilot randomized controlled trial (N=200 women) comparing two strategies of male partner involvement within the Option B+ program. In both arms (patient referral and contract referral) women will be encouraged to invite their male partners to accompany them to the clinic for couple HIV counseling and testing. In the contract referral arm, if the couple does not present within one week, the male partner will receive a home visit encouraging them to present to the clinic. We will compare the two arms for 1) uptake of couple HIV counseling and testing (cHCT), 2) uptake of cART for women, and 3) linkage to care for HIV-infected men. Results are expected to inform a larger trial and ultimately improve care-seeking in Malawi's HIV program.

Objective 1: Determine acceptability of male partner recruitment for cHTC within an Option B+ context. We will assess acceptability of eligible females to participate in this pilot RCT and reasons for non-participation.

Objective 2: Assess whether study arm (patient referral versus contract referral) is associated with cHTC uptake. We will conduct a pilot randomized controlled trial (RCT) of male partner recruitment. This study will contain two arms: patient referral and contract referral for uptake of cHTC (primary outcome).


Recruitment information / eligibility

Status Recruiting
Enrollment 330
Est. completion date January 2015
Est. primary completion date December 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 16 Years and older
Eligibility Inclusion Criteria:

- 18 years old or 16-17 years old and married

- Pregnant

- Received a positive HIV-test within the last day

- Will be in Lilongwe for the next month

- Able and willing to give locator information for >1 male partner in the Bwaila District Hospital catchment area (either a mobile number, a physical address, or both)

Exclusion Criteria:

- Enrolled/enrolling in the PROMISE study

- Initially Presenting with a male sex partner

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
contract referral
A female partner signs a contract saying it is permissible for a community worker to trace a male sex partner in the community.
patient referral
A patient agrees to recruit their partner using the invitation.

Locations

Country Name City State
Malawi Bwaila District Hospital Antenatal Unit Lilongwe Central District

Sponsors (1)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill

Country where clinical trial is conducted

Malawi, 

Outcome

Type Measure Description Time frame Safety issue
Primary Uptake of couple HIV counseling and testing It will be assessed whether the female partner brings her male partner to the antenatal clinic for couple HIV counseling and testing (as recorded on study case report forms). We will compare time to couple HIV counseling and testing between groups using the Kaplan Meier method and a log rank test. three months No
Secondary Female first Option B+ follow-up visit It will be assessed whether the female participants return for their first Option B+ visit (using the clinic's routine Option B+ records). Time to first visit will be assessed using a Kaplan Meier curve and a log rank test. three months No
Secondary Male linkage to care It will be assessed whether HIV-infected male partners are linked to care within one month of learning their HIV positive result with their partner. This will be assessed from abstraction of routine clinic records at Martin Preuss Center. We will use the Kaplan Meier method to plot outcomes and a log rank test to compare time to linkage to care between arms. one month No
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