Intimate Partner Study
- Conditions
- HIV/AIDSvoluntary male medical circumcision
- Registration Number
- PACTR201711002631294
- Lead Sponsor
- Impact Research and Development Organization
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 1800
Aged 20 and 49 years;
Uncircumcised;
Has a live-in/regular intimate partner with whom he intends to continue having sex
Able & willing to consent to join the study
Resident of study sub-locations
Not planning to relocate post-enrollment for at least six months
Outside 20 and 49 years age bracket
Circumcised
No live-in/regular sexual partner
Unable to or decline to provide consent
Non-residents of study Sub-locations
Intending to relocate within six months.
For Intervention 2, men will be excluded if the female partner declines to participate in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of men who come for VMMC services in the four study arms, within three months of intervention delivery
- Secondary Outcome Measures
Name Time Method Proportion reporting resuming sex before 6 weeks post-surgery, and for those who do, the time (days) they took to resume sex from date of circumcision;Proportion of participants between the intervention arms who advance from one stage to the next in the transtheoretical model;Proportion of men and women in the baseline interview who believe that female partners are shareholders in the man¿s decision to be circumcised; also compare participants¿ views in supporting women¿s involvement in VMMC programs