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CompletedNCT06324773Updated Jan 28, 2025

Prevalence of Postpartum Family Planning and Its Association With Spousal Joint Decision-Making in Family Planning

An observational study in Postpartum Family Planning, sponsored by Aga Khan University. Completed at 1 site in Pakistan. Open to participants aged 15 Years to 49 Years. Per ClinicalTrials.gov, last updated 2025-01-28.

Sponsored by Aga Khan University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
524
Ages
15 Years to 49 Years
Sex
All
01

Study summary

This community-based cross-sectional study investigates the prevalence of postpartum family planning (PPFP) uptake and its association with joint spousal family planning decision-making among married women in rural Sindh, Pakistan. The study, conducted in Thatta District with a population of approximately 0.98 million people, addresses sociodemographic challenges including high fertility rates, maternal and newborn mortality, and low contemporary contraception use. Targeting married women aged 18-49 who gave birth within the past year, the research utilizes data from the Global Network's Maternal and Newborn Health Registry. Data collection involves a pretested questionnaire administered by trained female data collectors. Statistical analysis includes descriptive statistics and logistic regression using STATA 17. The study aims to fill knowledge gaps regarding factors influencing PPFP uptake, particularly the role of joint decision-making in family planning. Findings could inform targeted interventions to enhance maternal and child health, contribute to existing knowledge, and guide policymakers and healthcare providers in addressing the unmet need for family planning in rural Pakistan.

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Conditions studied

  • Postpartum Family Planning
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In context

Lead sponsor

Aga Khan University is the lead sponsor of 290 studies on the registry; 44 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
15 Years to 49 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Married women of reproductive age (18-49) who gave birth a year ago and registered in the Maternal and Newborn Health Registry in Thatta District Sindh, Pakistan.

Inclusion criteria

  • Women who are married and gave birth a year ago
  • Living within the Maternal Neonatal Health Registry catchment area for at least one year.
  • Women who will give their consent.

Exclusion criteria

Exclusion Criteria:

  • Pregnant women.
  • Women who are critically ill and who face significant cognitive barriers that hinder their understanding and participation in the study.
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Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
524 participants (actual)
Target follow-up
3 Days
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. Prevalence of Postpartum Family Planning Uptake

    Number of women who utilized postpartum family planning.

    Time frame: In past one year

  2. Frequency of spousal joint decision making for uptake of postpartum family planning

    The outcome measures the frequency at which spouses make joint decisions regarding the uptake of postpartum family planning methods

    Time frame: In past one year

  3. Comparison between spousal joint decision making is using postpartum family planning method and non-users.

    Compare spousal joint decision-making in couples using postpartum family planning methods versus those not using them.

    Time frame: in past one year

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Study locations

1 site
  • Thatta
    Thatta, Sindh, Pakistan
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 28, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06324773
Lead sponsor
Aga Khan University
Responsible party
Shiyam Sunder, MBBS, MSc (Principal Investigator, Aga Khan University) — Principal investigator
First posted
Mar 22, 2024
Start date
Apr 1, 2024
Primary completion
Jul 30, 2024
Completion
Jul 30, 2024
Last update
Jan 28, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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