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AI and surveys aim to unlock family planning secrets in pakistan

NCT ID NCT06733831

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study surveys over 9,000 married women in Pakistan to understand why many who want modern contraceptives are not using them. Researchers will use AI and interviews to identify barriers like access, cost, or social norms. The goal is to help local programs better support women in making their own family planning choices.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this research could help design better family planning programs that address real barriers women face, potentially increasing voluntary contraceptive use.
What could go wrong
This is an observational study, not a treatment trial. It gathers information but does not test any intervention, so it cannot directly change outcomes. Results may not apply to other regions.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 9,230 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jul 2024

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population for this research focuses on Married Women of Reproductive Age (MWRA) between the ages of 15 and 49 residing in Sindh, Pakistan.

Ages

15 to 49 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Married women aged 15-49 * Married women providing written informed consent to participate in the study * One married woman from each selected household Exclusion Criteria: * Women below 15 years and above 49 years are not eligible to participate * Women aged 15-18 will be excluded unless a parent, guardian, or spouse consents to her participation in the study, * Participants who do not speak the languages in which the surveys and interviews are conducted may be excluded to ensure accurate communication and understanding of the study materials. * Individuals with severe cognitive impairments or intellectual disabilities that could affect their ability to comprehend the study objectives or provide meaningful responses may be excluded. * Participants who are unable or unwilling to provide informed consent for participation in the study will be excluded to uphold ethical standards and protect participant rights.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Aga Khan University

    Karachi, Sindh, 74800, Pakistan