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Recruiting NCT07376369

NCT07376369 Association of Spousal Support With Parenting Self-Confidence and Depression in Primipar Mothers

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Clinical Trial Summary
NCT ID NCT07376369
Status Recruiting
Phase
Sponsor Istanbul University - Cerrahpasa
Condition Support
Study Type OBSERVATIONAL
Enrollment 193 participants
Start Date 2026-01-30
Primary Completion 2027-01

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 193 participants in total. It began in 2026-01-30 with a primary completion date of 2027-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The transition to motherhood, particularly for first-time (primiparous) women, is a critical life period requiring substantial psychological and social adjustment. Hormonal changes, increased caregiving responsibilities, sleep disturbances, and potential social isolation during pregnancy and the postpartum period may increase vulnerability to stress, anxiety, and depressive symptoms. Postpartum depression (PPD) is a common mental health concern that adversely affects maternal well-being, mother-infant interaction, and infant development, with insufficient social support identified as one of its most significant risk factors. Maternal self-efficacy, defined as a mother's perceived competence in caring for and responding to her infant's needs, is a key indicator of successful adaptation to the parenting role. Evidence suggests that maternal self-efficacy develops primarily within the first months after childbirth and tends to be lower in primiparous women. Low parenting self-efficacy has been associated with increased depressive symptoms, higher parenting stress, impaired mother-infant bonding, and negative developmental outcomes for the infant. Among social support sources, partner support plays a particularly protective role during the transition to parenthood. Emotional, informational, and practical support provided by the partner has been shown to enhance maternal self-efficacy, reduce psychological distress, improve marital adjustment, and lower the risk of postpartum depression. Conversely, low perceived partner support and relationship difficulties are associated with an increased risk of PPD in primiparous mothers. The aim of this study is to examine the relationship between perceived partner support and postpartum parenting self-efficacy and depressive symptoms in primiparous women. Additionally, the study seeks to evaluate the explanatory and protective role of partner support on maternal self-efficacy and postpartum depression during the early postpartum period.

Eligibility Criteria

Inclusionsd Criteria: * Aged 18 years or older * Primiparous mothers (first childbirth) * Between 0 and 12 months postpartum * Living with spouse or partner * Able to read and write Turkish * Having access to the internet * Voluntarily agreeing to participate in the study Exclusion Criteria: * Diagnosed neurological disorder * Diagnosed psychiatric disorder * Visual impairment preventing completion of questionnaires * Cognitive impairment preventing completion of questionnaires

Contact & Investigator

Central Contact

Eslem Altıntaş, MSc

✉ eslem.altintas@acibadem.edu.tr

📞 +90 541 610 54 12

Principal Investigator

Merve Coşkun, Ph.D.

PRINCIPAL INVESTIGATOR

Acibadem University

Frequently Asked Questions

Who can join the NCT07376369 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Support. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07376369 currently recruiting?

Yes, NCT07376369 is actively recruiting participants. Contact the research team at eslem.altintas@acibadem.edu.tr for enrollment information.

Where is the NCT07376369 trial being conducted?

This trial is being conducted at Istanbul, Turkey (Türkiye).

Who is sponsoring the NCT07376369 clinical trial?

NCT07376369 is sponsored by Istanbul University - Cerrahpasa. The principal investigator is Merve Coşkun, Ph.D. at Acibadem University. The trial plans to enroll 193 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology