Talking it out: midwife sessions may ease pregnancy stress for couples
NCT ID NCT07663812
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
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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
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About 140 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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.
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The places running it
1 site. The list below names each one and where it is.
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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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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
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Yozgat City Hospital
RECRUITINGYozgat, Center, Turkey (Türkiye)