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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07663812
Acronym
ALEXITHYMIA
Enrollment
140
Registered
2026-06-23
Start date
2026-01-28
Completion date
2026-10-30
Last updated
2026-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Levels of Alexithymia During Pregnancy, Stress Levels During Pregnancy

Keywords

Levels of Alexithymia,, Levels of Stress,, Motivational Interviewing, Pregnant

Brief summary

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

Detailed description

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.

Interventions

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

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

Sponsors

Tokat Gaziosmanpasa University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Intervention model description

There are two parallel groups (experimental and control). The experimental group receives four sessions of motivational interviewing led by a midwife, while the control group receives routine prenatal education. Both groups undergo assessments before the intervention (pre-test) and after the intervention (post-test).

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
1. Stress Coping Styles Scale (SCSS):24 weeksCouples' 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.
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.24 weeks

Secondary

MeasureTime frameDescription
2. Toronto Alexithymia Scale (TAS):24 weeksCouples' 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.

Countries

Turkey (Türkiye)

Contacts

CONTACTESMA KIR
esma.kir@bozok.edu.tr+905550617545

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 27, 2026