跳至主要内容
临床试验/NCT03213028
NCT03213028已完成不适用

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 Pennsylvania1 个研究点 分布在 1 个国家目标入组 248 人开始时间: 2017年8月18日最近更新:
适应症
干预措施

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

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

Other

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

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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