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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
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03612518
Acronym
PPFP
Enrollment
970
Registered
2018-08-02
Start date
2018-09-15
Completion date
2019-08-01
Last updated
2018-08-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Contraception Behavior

Keywords

postpartum family planning, RCT, mhealth

Brief 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.

Interventions

BEHAVIORALText and Voice Messages

Participants 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 Call

Participants 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.

Sponsors

Junaid-ur-Rehman Siddiqui
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 44 Years
Healthy volunteers
No

Inclusion criteria

* Married * Pregnant women with gestational age up to 20 weeks * 15-44 years old throughout duration of study * Literate * Access to a cellphone * Living in the study's catchment area

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Postpartum Contraceptive UptakeThrough study completion, an average of six monthsProportion of subjects enrolled in each of the three groups who adopt any modern family planning method to delay next pregnancy
Skilled BirthThrough study completion, an average of six monthsProportion of women who gave birth in a health facility or through a skilled birth professional
ImmunisationThrough study completion, an average of six monthsProportion of women reported to immunise the newborn at birth

Secondary

MeasureTime frameDescription
Intention to Adopt Modern ContraceptionThrough study completion, an average of six monthsThe proportion of subjects enrolled in the program who state that they intend to adopt any modern family planning method to delay their next birth by 24 months (by type contraceptive method and time within 42 days of postpartum period)

Countries

Pakistan

Contacts

Primary ContactIshaque Sheikh, MSc
ishaque.sheikh@mariestopes.org.pk+92-111-538-538
Backup ContactJunaid-ur-Rehman Siddiqui, BBA
junaidrehman1994@hotmail.com+92-111-538-538

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026