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Clinical Trials in Turkey / NCT07139704
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The Effect of Mindfulness-Based Sexual Counseling on Body Appreciation, Sexual Distress, and Sexual Self-Confidence in Postpartum Women With Episiotomy

NCT07139704 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-09-20
Last updated
2025-08-24

Condition(s) studied

Postpartum Women

Investigational drug(s) / intervention(s)

Mindfulness-Based Sexual Counseling (MBSR-BA)

Mindfulness-Based Sexual Counseling (MBSR-BA): A MBSR-based sexual counseling program applied to women after episiotomy, 2 sessions per week for 4 weeks, 8 sessions in total.

Study summary

Aim: This study will aim to evaluate the effect of mindfulness-based sexual counseling on body appreciation, sexual distress, and sexual self-confidence in postpartum women with episiotomy.

Method: This randomized controlled experimental study will include participants assigned to intervention and control groups. The intervention group will receive a four-week mindfulness-based sexual counseling program consisting of eight sessions, while the control group will receive routine care. Body Appreciation, Sexual Distress, and Sexual Self-Confidence scales will be administered as pre- and post-tests.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
49 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Having had a vaginal birth and an episiotomy, * Having a follow-up appointment with the Family Health and Medical Center at 8 weeks postpartum, * Being able to read and write in Turkish, * Having a 3rd or 4th degree perineal tear Exclusion Criteria: * • History of pelvic surgery, * Significant psychiatric illness, * Presence of chronic illness that may affect sexual function

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kahramanmaraş Sütçü İmama Universty Kahramanmaraş Kahramanmaraş

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07139704 on ClinicalTrials.gov ↗ ← All trials in Turkey