Family Planning
Conditions
Brief summary
The goal of this pilot study is to assess both implementation outcomes (acceptability, feasibility and adoption) and clinical efficacy (contraceptive method uptake by women wishing to avoid pregnancy) using a Hybrid Type 2 study design of a family planning program being piloted by the Cervical Cancer Prevention Program in Gabarone, Botswana.
Interventions
OTHERWHO Decision-Making Tool for Family Planning Clients and Providers
Contraception decision-making tool
Sponsors
National Institute of Allergy and Infectious Diseases (NIAID)
University of Botswana
University of Pennsylvania
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No
Inclusion criteria
1. Female 2. English or Setswana speaking 3. Receiving CCP services at the clinic 4. 18-45 years of age 5. Able to give informed consent to study procedures, as determined by research/clinic staff
Exclusion criteria
1\. Pregnant
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Provider acceptability rating | 6 months | Likert scale 1-5, rating acceptability of offering family planning in this clinical setting. |
| Provider rating of feasibility | 6 months | Likert scale 1-5, rating feasibility of offering family planning in this clinical setting |
| Provider report of adoption of the intervention | 6 months | Comparing number of family planning methods offered by a provider pre- and post-intervention |
Countries
Botswana
Outcome results
None listed