Self-compassion training to improve sexual quality and marital adjustment in postpartum women
The Effect Of Awareness-Based Self-Compassage Educatıon Gıven To Women Experıenced Sexual Dysfunctıon In The Postpartum Perıod On The Qualıty Of Sexual Lıfe And Partnershıp
This study tests whether self-compassion training can help new moms improve their sexual health and relationships after childbirth.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 108 (estimated) |
| Sex | Female |
| Sponsor | Inonu University Academic / other |
| Locations | 1 site (Gaziantep) |
| Trial ID | NCT06632366 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of self-compassion training on the sexual quality of life and marital adjustment in women experiencing sexual dysfunction after childbirth. It focuses on the postpartum period, which can be challenging due to various physical and emotional changes. The intervention aims to provide support and education to help women navigate their sexual health and relationships during this transitional phase. Participants will be assessed for sexual dysfunction and will undergo training designed to enhance their self-compassion and overall well-being.
Who should consider this trial
Good fit: Ideal candidates are women between 2-6 months postpartum who are experiencing sexual dysfunction and have not yet resumed their menstrual cycle.
Not a fit: Patients who have undergone gynecological surgery during the study or have a current psychiatric illness may not benefit from this intervention.
Why it matters
Potential benefit: If successful, this intervention could significantly improve sexual satisfaction and relationship quality for postpartum women facing sexual dysfunction.
How similar studies have performed: While there is limited research specifically on self-compassion training for postpartum sexual dysfunction, similar approaches in related fields have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Erbal communicator and no literacy disability, * Living with his wife, * Beginning postpartum sexual intercourse, menstrual cycle has not started * Between 2-6 months postpartum, * Having a healthy baby * Menstrual cycle has not started * Women diagnosed with sexual dysfunction (total score ≥19) according to the Arizona * Sexual Experiences Scale will be included in the study. Exclusion Criteria: * Having undergone gynecological surgery during the study, * Have been or are currently diagnosed with a psychiatric illness, * Having attended any awareness-based training at least 6 months ago
Where this trial is running
Gaziantep
- Gaziantep Provincial Directorate of Health — Gaziantep, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Fadime Biçer Şahin, MSc
- Email: fadimebicer42@gmail.com
- Phone: 05522980842
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.