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Talking it out: midwife sessions may ease pregnancy stress for couples

NCT ID NCT07663812

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study tests whether motivational interviews led by midwives can lower stress and alexithymia (trouble identifying feelings) in pregnant women and their partners. About 140 couples will be split into two groups: one gets the motivational sessions, the other does not. Researchers will measure changes using standard stress and emotion scales before and after the intervention.

What this could mean

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

Active substance
motivational interviewing sessions led by midwives
What this could lead to
If it works, this could offer a simple, non-drug way to help pregnant couples cope with stress and emotional challenges.
What could go wrong
This is a small, early-stage study with no blinding or placebo, so results may be influenced by expectations. It only measures short-term changes.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 140 people

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

Started

Jan 2026

Expected to finish

Oct 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.

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: * For pregnant women: * Agreement to participate in the study * Being 18 years of age or older and married * Being in the second trimester * No pregnancy-related risks (such as preeclampsia, diabetes, heart disease, placenta previa, or oligohydramnios), * No issues related to fetal health (such as fetal anomalies or intrauterine growth restriction), * Ability to speak Turkish, * No history of chronic or psychiatric conditions, For partners: * Agreeing to participate in the study, * Accompanying their partner during the second trimester of pregnancy, * Not having a diagnosed psychiatric condition (depression, anxiety disorder, bipolar disorder, etc.), * Being able to speak and understand Turkish, Exclusion Criteria: * • Participants deciding to withdraw from the study at any stage, * Inability to contact the pregnant woman and/or her partner before the data collection process is completed, * The pregnant woman being diagnosed with a high-risk pregnancy during the data collection process.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

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.

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  3. A doctor treating you

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Contacts and locations

Locations

  • Yozgat City Hospital

    RECRUITING

    Yozgat, Center, Turkey (Türkiye)