An mHealth, Multi-Centre Randomized Controlled Trial to Promote Use of Postpartum Contraception Amongst Rural Women in Punjab, Pakistan
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 970
- 试验地点
- 4
- 主要终点
- Postpartum Contraceptive Uptake
研究概览
简要总结
Multiple encounters of pregnant women with the health care system during the late antenatal and immediate postpartum period provide a gateway for postpartum family planning counselling. Counselling on family planning services during this time is considered effective and cost-efficient for promoting healthy timing and spacing of pregnancies. This research aims to test the effectiveness of mobile phone-based interventions in promoting use of postpartum contraception.
详细描述
The study will be a three-arm, 10-month, multicentre, parallel-group, randomized controlled trial which will be conducted at 15 Suraj social franchise(SF) health facilities in Punjab province of Pakistan. Pregnant women aged 15-44 years who are in their first or second trimester and have a mobile phone for their own use will be eligible to participate in this study. The participants will be randomly allocated to one of three study arms: a) voice and text messages; b) interactive telephone-based counselling; or c) control arm (no additional phone-based support). The intervention counselling module will be developed based on the Integrated Behaviour Model which was recently adapted, and tested for the family planning context in Pakistan. It will broadly cover birth-preparedness, birth spacing and contraception, and postnatal care. The phone-based intervention aims to improve women's ability to use contraception by providing them with information about a range of methods, access to family planning methods through outlets such as Suraj SF providers, connecting them with MSS field health educators to help them reach the centres, motivation by re-enforcing the benefits of contraceptive use on women's quality of life, and dispelling myths and misconceptions about modern contraceptive methods. Risk differences will be used as the measure of effect of the intervention on the outcomes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 15 Years 至 44 Years(Child, Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Pregnant women with gestational age up to 20 weeks
- •15-44 years old throughout duration of study
- •Access to a cellphone
- •Living in the study's catchment area
排除标准
- •Not up to 20 weeks pregnant
- •Not between 15-44 years old for the study duration
- •Illiterate
- •Does not have regular access to a cellphone
- •Not residing within the catchment area
- •Does not provide consent to participate
研究组 & 干预措施
Text and Voice Messages
Participants will receive text messages and voice messages
干预措施: Text and Voice Messages (Behavioral)
Interactive Phone Call
Participants will receive interactive phone calls
干预措施: Interactive Phone Call (Behavioral)
Control
Participants in this arm will not be exposed to any intervention.
结局指标
主要结局
Postpartum Contraceptive Uptake
时间窗: Through study completion, an average of six months
Proportion of subjects enrolled in each of the three groups who adopt any modern family planning method to delay next pregnancy
Immunisation
时间窗: Through study completion, an average of six months
Proportion of women reported to immunise the newborn at birth
Skilled Birth
时间窗: Through study completion, an average of six months
Proportion of women who gave birth in a health facility or through a skilled birth professional
次要结局
- Intention to Adopt Modern Contraception(Through study completion, an average of six months)
研究者
Junaid-ur-Rehman Siddiqui
Principal Investigator
Marie Stopes Society
