Behavioural Insights to Improve Take up of SRH Services (Uganda)
2017年6月9日 更新者:Marie Stopes International
Applying Behavioural Insights to Improve Take up of Sexual and Reproductive Health Services
This is a randomised controlled trial to test the impact of a modified e-coupon service, delivered through SMS, on uptake of sexual and reproductive health services among women calling a free hotline in Uganda.
研究概览
详细说明
The overall goal of the proposed research project is to increase uptake of sexual and reproductive health (SRH) services among clients who call into Marie Stopes Uganda's free hotline.
The study seeks to achieve this goal by using behavioural economics to design interventions to increase redemptions of e-coupons distributed to hotline clients.
The intervention will include modifying the text message sent to e-coupon recipients as well as sending follow-up texts reminding clients to use their coupons.
The impact of the intervention will be evaluated using a randomized controlled trial (RCT).
The intervention will be implemented and data will be collected regularly over a period of approximately 12 months.
Strict confidentiality procedures in line with Marie Stopes International's best practices will be put into place to ensure that information made public or otherwise distributed outside the principle investigators and other key personnel cannot be linked to any individual respondents.
Results from the study will be published in a report, among other outputs, and the outcomes will be shared within MSI as well as with the wider SRH community.
研究类型
介入性
注册 (预期的)
2000
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Olivia Nuccio, MSc
- 邮箱:olivia.nuccio@mariestopes.org
研究联系人备份
- 姓名:Kathryn Church, PhD
- 邮箱:kathryn.church@mariestopes.org
学习地点
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Kampala、乌干达
- 招聘中
- Marie Stopes Uganda call centre
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接触:
- Lianne Hawkins, MSc
- 电话号码:+256 393 263318
- 邮箱:lianne.hawkins@mariestopes.or.ug
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 及以上 (成人、年长者)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- Callers to the call centre who are over the age of 18, receive an e-coupon, and consent to participate in the research.
Exclusion Criteria:
- Callers who are below the age of 18, non-recipients of e-coupons, and those who receive e-coupons but do not consent to participate in the study.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Treatment group (modified text)
The treatment group will receive a modified text of the current e-coupon.
They will also receive notification that they have been enrolled in the study via a second text.
They will also receive a series of text message reminders to redeem their e-coupons at intervals of 6, 13 and 18 days after coupon origination.
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The treatment group will receive a modified text of the current e-coupon.
They will also receive notification that they have been enrolled in the study via a second text.
They will also receive a series of text message reminders to redeem their e-coupons at intervals of 6, 13 and 18 days after coupon origination.
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假比较器:Control group (standard text)
Participants receive control text (SMS) message, which contains a numeric coupon code and no additional text to the standard coupon.
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Participants receive control text (SMS) message, which contains a numeric coupon code and no additional text to the standard coupon.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
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Increase in e-coupon redemption in MSU centres
大体时间:6 months
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Increase in proportion of e-coupons redemmed in MSU centres within 6 months of intervention
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6 months
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Increase in SRH service uptake in MSU centres
大体时间:6 months
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Increase in the proportion of participants taking up an SRH service (of any kind) in an MSU centre within 6 months
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6 months
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
合作者
调查人员
- 首席研究员:Karina Lorenzana、Ideas42
- 首席研究员:Patricia Aujo、Marie Stopes International
- 首席研究员:Andrew Fertig, PhD、Ideas42
- 首席研究员:Andrew Gidudu, MSc、Marie Stopes International
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2016年3月1日
初级完成 (预期的)
2017年7月1日
研究完成 (预期的)
2017年9月1日
研究注册日期
首次提交
2016年7月18日
首先提交符合 QC 标准的
2017年5月22日
首次发布 (实际的)
2017年5月23日
研究记录更新
最后更新发布 (实际的)
2017年6月12日
上次提交的符合 QC 标准的更新
2017年6月9日
最后验证
2017年6月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.
健康行为的临床试验
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University of Colorado, DenverEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD); National... 和其他合作者主动,不招人