Family Planning Service Delivery Integration For HIV Positive And At-Risk Women In Botswana: A Hybrid Type 2 Clinical Intervention And Implementation Strategy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 248
- 试验地点
- 1
- 主要终点
- Provider rating of feasibility
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 45 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •English or Setswana speaking
- •Receiving CCP services at the clinic
- •18-45 years of age
- •Able to give informed consent to study procedures, as determined by research/clinic staff
排除标准
- 未提供
研究组 & 干预措施
Full group
Our goal is to assess the feasibility and acceptability of incorporating family planning (FP) service delivery, using a program validated by the World Health Organization (WHO), into the established Cervical Cancer Prevention (CCP) programs of Botswana.
干预措施: WHO Decision-Making Tool for Family Planning Clients and Providers (Other)
结局指标
主要结局
Provider rating of feasibility
时间窗: 6 months
Likert scale 1-5, rating feasibility of offering family planning in this clinical setting
Provider report of adoption of the intervention
时间窗: 6 months
Comparing number of family planning methods offered by a provider pre- and post-intervention
Provider acceptability rating
时间窗: 6 months
Likert scale 1-5, rating acceptability of offering family planning in this clinical setting.
次要结局
未报告次要终点
