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War's hidden toll: new study to examine reproductive decisions and mental health in ukrainian women

NCT ID NCT07551934

Knowledge-focused Sponsor: Taras Shevchenko National University of Kyiv Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 12, 2026 · Updated 2 times

Summary

This observational study will survey over 300 Ukrainian women to understand how war influences their decisions about pregnancy and childbirth, and their mental health during the perinatal period. Participants will complete questionnaires about their well-being, reproductive choices, and experiences of war. The goal is to build a model that explains the factors affecting reproductive behavior and mental health in wartime.

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 study could provide a better understanding of how war impacts women's reproductive choices and mental health, potentially guiding future support programs.
What could go wrong
This is an observational study, not a treatment trial. It cannot prove cause and effect, and results may not apply to other populations or conflict settings.

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 328 people

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

Started

Jul 2026

Expected to finish

Nov 2028

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

Women will be recruited in Ukraine from healthcare settings providing reproductive, gynecological, pregnancy-planning, antenatal, childbirth, and postpartum care. The source population includes women across the reproductive continuum, including those not currently planning pregnancy, those planning pregnancy, those with an ongoing pregnancy, and those within 12 months after childbirth. Where feasible, consenting partners of enrolled women will also be included.

Ages

18 years and older

Sex

Anyone

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: * able and willing to provide informed consent; * aged 18 years or older. Exclusion Criteria: * younger than 18 years; * unable to provide informed consent; * do not have sufficient language proficiency to complete the study procedures; * at the time of recruitment, they have an acute medical or psychological condition that would make participation unsafe, inappropriate, or unduly burdensome (e.g., obstetric emergencies, immediate postoperative or critical care status, or severe acute distress requiring urgent clinical care); * participation or the handling of personal data could reasonably pose a risk to the safety of the participant or their family.

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Conditions

The condition(s) this trial relates to.

post-traumatic stress disorder postpartum depression Psychological Trauma Psychological Well-Being Reproductive Behavior

As listed by the trial registrant

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

Cohort studies Perinatal mental health Reproductive behavior Women

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Taras Shevchenko National University of Kyiv

    RECRUITING

    Kyiv, Ukraine

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