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Efficacy of Cognitive Behavior Therapy on Sexual function and satisfaction among post-menopausal women

Efficacy of Cognitive Behavior Therapy on Sexual function and satisfaction among post-menopausal women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015100324322N1
Enrollment
4
Registered
2016-07-08
Start date
2015-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Menopause sexual dysfunction. Other specified menopausal and perimenopausal disorders

Interventions

Behavior
Single case( multiple baseline), intervention will be held 8 sessions of 90 minutes according to researcher-made protocol based on cognitive behavioral therapy for every four participants held weekly.

Sponsors

Research Committee, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: menopausal women aged between 45- 60 year old (at least one year after amenorrea); married with stable life with her husband; first married; natural menopause; monogamy; FSFI<26; ISS<75; minimum education: diploma and accessible for 6 months. Exclusion criteria: not having sex during the study; vaginal/ cervical/ pelvic infection( by examination); diagnosed psychological illness; history of sexual abuse or sexual harassment; addiction ( alcohol, drugs and other psychotropic drugs); occurrence of mishap events ( death, accidents with disabilities, treason, etc.) during the last 6 months; chronic diseases affect sexuality for menopausal women or her husband such as diabetes, cardiovascular disease, hypertension, cancer, vascular damage caused by accidents, thyroid disorders, spinal disorders, parkinson's disease, MS; the use of hormone replacement therapy (HRT) or topical estrogen for last 6 months.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Menopausal sexual function. Timepoint: Before intervention, during intervention, two months after intervention. Method of measurement: Female sexual function index (FSFI).;Menopausal sexual satisfaction. Timepoint: Before intervention, during intervention, two months after intervention. Method of measurement: Female sexual function index (FSFI).;Menopausal sexual distress. Timepoint: Before intervention, during intervention, two months after intervention. Method of measurement: Female sexual function index (FSFI).

Secondary

MeasureTime frame
Sexual desire in menopausal wemon. Timepoint: Before intervention, during intervention, two months after intervention. Method of measurement: Female Sexual Function Index.;Sexual arousal in menopausal wemon. Timepoint: Before intervention, during intervention, two months after intervention. Method of measurement: Female Sexual Function Index.;Sexual lubrication in menopausal wemon. Timepoint: Before intervention, during intervention, two months after intervention. Method of measurement: Female Sexual Function Index.;Orgasm in menopausal wemon. Timepoint: Before intervention, during intervention, two months after intervention. Method of measurement: Female Sexual Function Index.;Sexual satisfaction in menopausal wemon. Timepoint: Before intervention, during intervention, two months after intervention. Method of measurement: Female Sexual Function Index.;Sexual pain in menopausal wemon. Timepoint: Before intervention, during intervention, two months after intervention. Method of measurement: Female Sexual Function Index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHajar Haghighi

Ahwaz Jundishapur University of Medical Sciences

haghighi.h@ajums.ac.ir; negar8606@yahoo.com+98 611336754360

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026