ACTRN12619000378123已完成未知
Quasi-experimental pretest-post-test study to determine the number of new users of contraception amongst women 15-49 years old before and after introduction of a community and provider driven social accountability intervention.
Department of Reproductive Health and Research, which includes the the UNDP/UNFPA/UNICEF/WHO/World Bank Special Programme of Research, Development, World Health Organization0 个研究点目标入组 4,700 人开始时间: 2019年3月11日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 4,700
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Educational / counselling / training
入排标准
- 年龄范围
- 15 Years 至 65 Years（—）
- 性别
- All
入选标准
- •For the measurement of changes in contraceptive uptake (facility audit), facilities meeting the following inclusion criteria will be included:
- •Providing family planning
- •In the study catchment area
- •Public and where cost is not a barrier to access at the point of access by the client
- •Agree to participate in the study
- •Recorded family planning service data
- •For measurement of changes in contraceptive use (cohort study), individuals meeting the following inclusion criteria will be included:
- •Women aged 15-49
- •Accessing family planning at a participating study facility
- •First time using contraception in previous 6 months
- •New” users of family planning methods are defined as clients who have:
- •-Never used a family planning method (new acceptors)
- •-Are switching from a traditional to a modern family planning method (additional users)
- •-Are re-starting a family planning method after a period of not using it for at least 6 months (additional users)
- •Willing to/anticipates to stay in the study area/district during the period of the study.
- •Providing consent to participate
- •For evaluating social accountability intermediate outcomes (cross sectional survey), the following inclusion criteria are used:
- •Health professionals:
- •Health professionals working in the intervention facility.
- •Women from the community:
- •Women aged 15 to 49 years
- •Accessing family planning at a participating study facility
- •First time or continuing users of contraception
- •Providing consent to participate
- •For the process evaluation, participants will be purposively and snowball sampled based on criteria including their exposure to the social accountability intervention or their role, such as a health provider or duty bearer.
排除标准
- •For measurement of changes in contraceptive uptake (facility audit), the following exclusion criteria will be used:
- •Facilities:
- •Where fee for service acts as barrier to access
- •Outside the study catchment area
- •Not providing regular family planning services
- •Do not agree to participate
- •Do not record regular family planning service data
- •For measurement of changes in contraceptive use (cohort study), the following exclusion criteria will be used:
- •Women below 15 or over 49
- •Women who desire to/wish to become pregnant
- •Women who have used contraception in the past 6 months
- •Women who are unable or unwilling to provide consent to participate
- •For evaluating social accountability intermediate outcomes (cross sectional survey), the following inclusion criteria are used:
- •Exclusion criteria for health professional:
- •Health professionals who are unable or unwilling to agree to participate
- •Exclusion criteria for women from the community:
- •Women below 15 years
- •Women who are unable or unwilling to provide consent to participate
研究者
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