Family Planning Service Delivery Integration For HIV Positive And At-Risk Women In Botswana: A Hybrid Type 2 Clinical Intervention And Implementation Strategy

University of Pennsylvania248 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Enrollment

248

Conditions

Family Planning

Interventions

WHO Decision-Making Tool for Family Planning Clients and ProvidersOTHER

Contraception decision-making tool

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 45 Years

Medical Language ↔ Plain English

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

Locations (1)

Princess Marina Hospital

Gabarone, Botswana

Outcomes

Primary Outcomes

Provider acceptability rating

Likert scale 1-5, rating acceptability of offering family planning in this clinical setting.

Time frame: 6 months

Provider rating of feasibility

Likert scale 1-5, rating feasibility of offering family planning in this clinical setting

Time frame: 6 months

Provider report of adoption of the intervention

Comparing number of family planning methods offered by a provider pre- and post-intervention

Time frame: 6 months

Data from ClinicalTrials.gov

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