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NCT Number: NCT07663812

THE EFFECT OF MOTIVATIONAL INTERVENTIONS LED PREGNANCY ON STRESS AND ALEXITHYMIA IN COUPLES

The aim of this study is to examine the effect of midwife-led motivational interviewing during pregnancy on couples' stress and alexithymia levels.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Yozgat City Hospital

Yozgat, Center, Turkey (Türkiye)

Location status: Recruiting

Location contact

ESMA KIR

CONTACT

[email protected]

05550617545

About this study

This study aims to evaluate the effect of midwife-led motivational interviewing during pregnancy on couples' stress coping skills and levels of alexithymia. Designed as a randomized controlled trial, the study includes healthy pregnant women in their second trimester and their partners. The intervention group receives midwife-led motivational interviewing, while the control group receives routine care. Data are collected using the Demographic Information Form, the Coping Styles Scale, and the Toronto Alexithymia Scale. The study results will determine whether midwife-led motivational interviews are an effective intervention for supporting psychological well-being during pregnancy through a couple-centered approach.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

a group where motivational sessions are held for pregnant women and their partners

Other

a group where motivational sessions are held for pregnant women and their partners

Primary outcomes

  1. 1. Stress Coping Styles Scale (SCSS):

    Time frame: 24 weeks

    Couples' stress coping skills are being assessed. The assessment is administered twice: as a pre-test (at the beginning) and a post-test (after the intervention). Both the total scale score and the subscale scores are used.

  2. 1. Stress Coping Styles Scale (SCSS): This scale assesses couples' stress coping skills. It is administered twice: at the pre-test (baseline) and post-test (post-intervention). Both the total scale score and the subscale scores are used.

    Time frame: 24 weeks

Secondary outcomes

  1. 2. Toronto Alexithymia Scale (TAS):

    Time frame: 24 weeks

    Couples' levels of alexithymia are being assessed. The assessment is administered twice: as a pre-test (at the beginning) and a post-test (after the intervention). Both the total scale score and the subscale scores are used.

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Tokat Gaziosmanpasa University

Other

Registry information

Official study title

THE EFFECT OF MOTIVATIONAL INTERVENTIONS LED BY MIDWIVES DURING PREGNANCY ON STRESS AND ALEXITHYMIA IN COUPLES

Acronym: ALEXITHYMIA

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 23, 2026
Registry last updated
Jun 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.