Ireland
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Recruiting Not applicable

The Effect of Self-Compassion Training on Sexual Life Quality and Marital Adjustment in Women With Sexual Dysfunction

NCT06632366 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-02-05
Last updated
2024-10-09

Condition(s) studied

Postpartum Sexual Dysfunction

Investigational drug(s) / intervention(s)

Sexual Dysfunction in the Postpartum Period

Sexual Dysfunction in the Postpartum Period: The experimental group will receive mindfulness-based self-compassion training. The control group will not receive any intervention.

Study summary

Sexual function in the postpartum period, the gateway to newness and change, can be affected by problems such as caring for a new baby, breastfeeding, fatigue, anxiety about pain during sexual intercourse, postpartum depression, pelvic floor dysfunction, urinary symptoms and body image. Changes in sexual function are common in the postpartum period. Pregnancy and childbirth is a period in a woman's life that causes hormonal and physical changes and has an impact on the parents' quality of life.

Postpartum sexual function is an important issue for couples, as the first sexual intercourse after childbirth is an important step for couples to establish intimate relationships. Many factors affect postpartum sexual dysfunction, including number of births, breastfeeding, mode of delivery, episiotomy, physical and psychological dysfunction, including fatigue and postpartum depression. Without adequate information and counseling on sexual life by health professionals in the postpartum period, most women may remain silent about their sexual concerns and anxieties, preferring instead to share their problems with friends. More holistic and multidisciplinary approaches are needed to treat female sexual dysfunctions. The use of mindfulness-based therapies has recently become widespread in the treatment of women diagnosed with sexual dysfunction.Thanks to mindfulness practices, it has been observed that women perceive stimuli better and are able to notice clues that they did not notice before. The Compassion Focused Therapy program is one of these practices. It is known to integrate well with existing approaches to therapy and offers some useful ways of reducing sexual problems to provide a coherent rationale for treatment strategies.

Eligibility

Sex
FEMALE
Min age
—
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

  • Arizona Sexual Experiences Scale- Female (ASES-F) — ten weeks
    The female form includes questions investigating sexual drive, psychological arousal, physiological arousal (vaginal lubrication), the capacity to reach orgasm and the feeling of satisfaction after orgasm. Each question in the scale is scored from 1 to 6, and the minimum score that can be obtained from the total score is 5 and the maximum is 30. A total score of 19 and above from the scale, a score of 5 or 6 for any item or a score of 4 for three or more items indicates the presence of sexual dysfunction. While low scores represent that the sexual response is effective, comfortable and satisfying, high scores indicate the presence of sexual dysfunction. The total internal consistency coefficient of the scale is 0.89 and the Cronbach alpha reliability coefficient is 0.90.

Trial sites (1)

FacilityCityRegionStatus
Gaziantep Provincial Directorate of Health Gaziantep Turkey (Türkiye) Recruiting
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 NCT06632366 on ClinicalTrials.gov ↗ ← All trials in Turkey