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UnknownNCT03612518

An mHealth Trial to Promote the Use of Postpartum Contraception

An mHealth, Multi-Centre Randomized Controlled Trial to Promote Use of Postpartum Contraception Amongst Rural Women in Punjab, Pakistan

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
970 (estimated)
Sponsor
Junaid-ur-Rehman Siddiqui · Academic / Other
Sex
Female
Age
15 Years – 44 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALText and Voice MessagesParticipants in this study arm will periodically receive information regarding antenatal- and postnatal care and family planning services through text and voice messages from the fifth gestational month until the post-partum period of 42 days.
BEHAVIORALInteractive Phone CallParticipants in this study arm will receive information regarding antenatal- and postnatal care and family planning services through periodic interactive phone calls from the fifth gestational month until the post-partum period.

Timeline

Start date
2018-09-15
Primary completion
2019-08-01
Completion
2019-08-01
First posted
2018-08-02
Last updated
2018-08-02

Locations

4 sites across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT03612518. Inclusion in this directory is not an endorsement.