- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01857700
Economic Compensation to Increase Demand for Voluntary Medical Male Circumcision (CTT-VMMC)
Compensation for Transport Costs and Lost Wages Associated With Voluntary Medical Male Circumcision (VMMC) Uptake: an Intervention to Increase VMMC Demand Among Older Men in Nyanza Province
Research questions: What effect does provision of food vouchers have on uptake of voluntary medical male circumcision? What is the amount of food voucher that should be given?
Hypothesis: The percentage of men who are compensated for costs of travel to and lost wages due to VMMC and who undergo VMMC will be higher than the percentage of men who are compensated for lost wages or travel and undergo VMMC, and both of these percentages will be higher than the percentage of men who are not compensated for travel or lost wage costs but undergo VMMC.
Study Overview
Status
Detailed Description
Purpose: Implement a randomized trial to test whether offering compensation to older men conditional on their coming for medical male circumcision can increase uptake of circumcision services.
Participants: 1,500 uncircumcised men of ages 25-49 in Nyando District, 21 men who chose to be circumcised and 21 who did not get circumcised, 10 female partners of men who became circumcised and 10 female partners of men who did not will be interviewed
Procedures (methods): To increase uptake of male circumcision, investigators will offer conditional economic compensation for male circumcision. Randomly selected study participants will be given the opportunity, conditional on undergoing male circumcision, to obtain food vouchers that are intended to offset the cost of accessing the VMMC services and the potential lost work the day of the procedure and in the 2 days following the procedure. The food vouchers will be given after study participants choose to uptake VMMC services at any of the static or outreach sites operated by Impact Research and Development Organization (IRDO). Participants will be randomized to one of three intervention groups or to a control group. Participants in the intervention groups will have the opportunity to receive a food voucher valued at one of three amounts (in KES, Kenyan Shillings) if they choose to get circumcised. Participants in the control group will receive a soda but no food voucher if they choose to get circumcised. The amounts for the intervention groups were selected based on the approximate value of 3 days of work and average transportation costs within the district. The amounts were also chosen so that they are not so large as to be perceived as coercive. Investigators selected food vouchers instead of cash or mobile phone credit because the vouchers were deemed to be more acceptable given the sensitive nature of the intervention and men's concern with feeding their families; it was also considered more logistically feasible to offer vouchers at the health facilities rather than cash. Additional focus group discussions will be held to verify that this form and amount of compensation is acceptable and desirable in study communities and if necessary, the intervention can be changed based on these results.
The food vouchers will be valid at dukas (shops) located within the district. At the beginning of the study, these shops will be visited and informed about ways to receive cash for the vouchers at the central IRDO office in Nyando District. IRDO has previously explored the feasibility of implementing the voucher scheme and found that it can be implemented in the study areas.
Three months after enrollment of study participants, investigators will conduct qualitative research in which there will be in-depth interviews with a small sample of men who did and did not come for circumcision and with their partners. Three topics will be examined in the qualitative interview: men's decision-making, logistics of the intervention, and women's perceptions.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Nyanza
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Kisumu, Nyanza, Kenya
- Impact Research & Development Organization
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Men
- aged 25-49
- living in enumerated locations and sublocations of Nyanza Province
- who intend to remain in their village for the next three months.
Female partners of some of these eligible men are also eligible to be interviewed about their perceptions.
Exclusion Criteria:
Men
- younger than 25,
- older than 49, or
- intending to move away from their village within three months.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Placebo Comparator: Standard of Care
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Consistent with standard of care, participants in this group will be offered a refreshment during their office visit.
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Experimental: Conditional economic compensation
A scratch off card will be used to randomly determine which of the compensations will be offered: compensation for transport cost, compensation for lost wages, or compensation for transport cost and lost wages
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
percentage who undergo voluntary medical male circumcision
Time Frame: 14 weeks
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14 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Qualitative Outcome Measure #1: men's decision-making around circumcision, including how the food voucher affected their decision and communications with their female partners surrounding circumcision.
Time Frame: 14 weeks
|
men's concerns with circumcision (i.e., what man had heard about circumcision prior to enrollment; what man had thought about getting circumcised prior to enrollment; greatest concern with getting circumcised prior to enrollment; degree of financial barrier prior to enrollment), experience with how food voucher was explained (i.e., what man was told about voucher amount, what man was told about reason for voucher, what man was told about how it could be redeemed, whether anything was unclear, whether questions were answered satisfactorily), what was discussed with a female partner (i.e., whether circumcision had ever been discussed; her opinion of it; whether the study and food voucher were discussed and what was discussed; her opinion of the study and food voucher; her opinion of whether man should get circumcision; whether partner's opinions influenced man's decision about whether to go for circumcision)
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14 weeks
|
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Qualitative Outcome Measure #2: impact of food voucher intervention on man
Time Frame: 14 weeks
|
the effect of the food voucher on the man (i.e., whether it was volunteered as the biggest reason for deciding to get circumcised; whether it had changed his mind about getting circumcised; whether the value of the food voucher made it easier or more difficult to decide about getting circumcised)
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14 weeks
|
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Qualitative Outcome Measure #3: impact of intervention logistics on man
Time Frame: 14 weeks
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use of food voucher (i.e., whether redeeming it with 30 days was a constraint; whether there were any problems with redeeming it) and transportation & time away from work (i.e., distance between residence and nearest circumcision clinic; transportation to clinic and its total cost, number of days missed from work and lost wages because of missed work; whether the food voucher offset the costs of transportation and lost wages).
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14 weeks
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Qualitative Outcome Measure #4: couple's decision-making around circumcision (including how the food voucher affected their decision and communications with male partners surrounding circumcision) as reported by female partner
Time Frame: 14 weeks
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woman's concerns with circumcision (i.e., what woman had heard about circumcision prior to partner's enrollment; what woman had thought about getting circumcised prior to partner's enrollment; greatest concern with partner getting circumcised prior to his enrollment; degree of financial barrier prior to enrollment), experience with how food voucher was explained (i.e., what woman was told about voucher amount, what woman was told about reason for voucher, what woman was told about how it could be redeemed, whether anything was unclear, whether questions were answered satisfactorily), what was discussed with a partner (i.e., whether circumcision had ever been discussed; her opinion of it; whether the study and food voucher were discussed and what was discussed; partner's opinion of the study and food voucher; his opinion of whether he should get circumcision; whether her opinions influenced man's decision about whether to go for circumcision)
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14 weeks
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Qualitative Outcome Measure #5: impact of food voucher intervention on couple, as reported by female partner
Time Frame: 14 weeks
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the effect of the food voucher on the couple (i.e., whether it was volunteered as the biggest reason for deciding that man would get circumcised; whether it had changed couple's mind about getting circumcised; whether the value of the food voucher made it easier or more difficult for couple to decide about getting circumcised)
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14 weeks
|
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Qualitative Outcome Measure #6: impact of intervention logistics on couple, as reported by female partner
Time Frame: 14 weeks
|
use of food voucher (i.e., whether redeeming it with 30 days was a constraint for the couple; whether there were any problems for the couple with redeeming it) and transportation & time away from work (i.e., distance between residence and nearest circumcision clinic; transportation to clinic and its total cost, number of days missed from work and lost wages because of missed work; whether the food voucher offset the costs of transportation and lost wages).
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14 weeks
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Collaborators and Investigators
Investigators
- Principal Investigator: Harsha Thirumurthy, PhD, UNC-Chapel Hill, CPC and SPH-HPM
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 12-1961
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