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Clinical Trials/NCT03594305
NCT03594305
Completed
N/A

From Obstacles to Opportunities for Family Planning in Tanzania

Weill Medical College of Cornell University1 site in 1 country24 target enrollmentAugust 20, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Contraception Behavior
Sponsor
Weill Medical College of Cornell University
Enrollment
24
Locations
1
Primary Endpoint
Uptake of family planning at village dispensaries
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The investigators will conduct a cluster randomized trial to determine the effectiveness of an educational intervention for religious leaders in promoting uptake of family planning in Tanzania.

Detailed Description

In this community randomized trial, the investigators will randomize 12 rural villages to receive an educational seminar for their religious leaders about family planning. The investigators will compare these uptake of family planning in these 12 villages with 12 matched villages whose religious leaders do not attend an educational seminar about family planning. The investigators will also determine women's reasons for seeking family planning at the village dispensaries.. Prior to the start of the trial, the study team will ensure that dispensaries in all villages in the trial will have a reliable supply of contraceptive options. To mitigate the effect of economic barriers and medication shortages on access to contraception, a dedicated medication supply team will make certain that all dispensaries remain well-stocked with standard contraceptives that are free from the Tanzanian Ministry of Health. These include oral contraceptive pills, implants, injections, copper intrauterine devices, and condoms. Villages will be paired by proximity (within 50 kilometers of one another). Within the pair, one village will be randomly assigned, using a computer-generated algorithm, to receive the intervention of religiously- and culturally-informed teaching intervention about family planning for religious leaders. The other village will be the control village. Each intervention village will be followed, and its religious leaders mentored in groups, for 12 months after the start of the intervention. Mentorship groups of 25 leaders, led by the study team, will meet for 1 hour per month. The investigators will also conduct focus groups in both intervention and control villages to understand community perceptions of family planning.

Registry
clinicaltrials.gov
Start Date
August 20, 2018
End Date
June 2, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Rural villages in northwest Tanzania with populations between 8,000 and 20,000
  • Village dispensaries present to measure uptake of family planning
  • Located in close proximity (50 km or less) to another eligible village with which it can be paired

Exclusion Criteria

  • Private dispensaries at which family planning uptake would be missed

Outcomes

Primary Outcomes

Uptake of family planning at village dispensaries

Time Frame: 12 months

The investigators will measure the percent of the population seeking modern contraception.

Secondary Outcomes

  • Pregnancy rates(12 months)
  • Couple-years of protection(12 months)
  • Reasons for seeking family planning(12 months)

Study Sites (1)

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