An mHealth Trial to Promote the Use of Postpartum Contraception

Status Not yet recruiting

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Contraception Behavior

Clinical Trial Details

NCT number	NCT03612518
Study type	Interventional
Source	Marie Stopes Society
Contact	Ishaque Sheikh, MSc
Phone	+92-111-538-538
Email	ishaque.sheikh@mariestopes.org.pk
Status	Not yet recruiting
Phase	N/A
Start date	September 15, 2018
Completion date	August 1, 2019

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05889689` - Evaluation of an Adolescent Pregnancy Prevention Program; Relationship Smarts+ With Lessons From Mind Matters	N/A
Withdrawn	`NCT03725358` - A Cluster-RCT to Increase the Uptake of LARCs Among Adolescent Females and Young Women in Cameroon.	N/A
Completed	`NCT02234271` - Plan A Birth Control: Randomized Controlled Trial of a Mobile Health Application for Contraception Information	N/A
Recruiting	`NCT05216003` - Pregnancy at a Time That Is Happy and Healthy for You
Completed	`NCT04136613` - Utility of Immediate Post Placental Insertion of Intrauterine Device During Cesarean Delivery	N/A
Completed	`NCT03366636` - Project Legacy Impact Evaluation Study	N/A
Recruiting	`NCT06100679` - Responsible Engaged and Loving (REAL) Fathers Intervention Evaluation	N/A
Completed	`NCT03775642` - Debunking Myths About Contraceptive Safety Among Women in Kingston, Jamaica	N/A
Completed	`NCT03571932` - Assessment of Family Planning and Immunization Service Integration in Liberia
Completed	`NCT03165838` - Effectiveness of Shortened Time Interval to Postpartum Visit in Improving Postpartum Attendance	N/A
Completed	`NCT04120376` - Reducing Adolescent Pregnancy	N/A
Completed	`NCT03400410` - Hormonal Contraceptive Health Education for Adolescent Males	N/A
Not yet recruiting	`NCT05988983` - The Over The Counter Pill National Study
Not yet recruiting	`NCT05362019` - Effects of One-to-one Service on the Continuation and Satisfaction of Contraceptive Use.	N/A
Completed	`NCT01360216` - Cluster, Randomized Trial on Long Acting Reversible Contraception (LARC) Education and Training	N/A
Completed	`NCT03559634` - Contraception Initiation Feasibility in the Pediatric ED	N/A
Enrolling by invitation	`NCT05022134` - Evaluating the Impact of CHOICE-AYA on Contraceptive Use, Continuation and Satisfaction	N/A
Active, not recruiting	`NCT03733678` - A Randomized-Controlled Trial to Increase the Uptake of LARCs in Cameroon	N/A
Completed	`NCT03500978` - Factors Predicting Ineffective Contraception Use	N/A
Recruiting	`NCT06307002` - Evaluating What's My Method? in Barbados	N/A

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

An mHealth Trial to Promote the Use of Postpartum Contraception — PPFP

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms