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The effect of mindfulness-based sex therapy on female sexual desire disorder, distress self-disclosure and sexual function

The effect of mindfulness-based sex therapy on female sexual desire disorder, distress self-disclosure and sexual function

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160808029255N4
Enrollment
70
Registered
2018-09-17
Start date
2018-05-15
Completion date
Unknown
Last updated
2021-06-21

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

Conditions

Condition 1: Sexual desire. Condition 2: sexual disstress. Condition 3: Sexual self-discloser. Condition 4: Sexual function. Hypoactive sexual desire disorder Other sexual dysfunction, not caused by organic disorder or disease

Interventions

Intervention 1: Intervention group: The intervention group will be receive four-weekly sessions for 90 to 120 minutes. intervention including sex education, mind-boggling exercises, behavioral therapy

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Age of 15-49 years have been married being sexually active having alive spouse not being pregnant not being in lactation period do not use contraceptive drugs that has an effect on sexual desire lack of spouse's sexual dysfunction having at least high school education having marital and interpersonal relationships satisfaction not having other sexual disorders except sexual desire disorder

Exclusion criteria

Exclusion criteria: having or positive history of well-known psycho-somatic diseases that interfere with marital relationships daily activities using sexually-suppressive drugs (such as low blood pressure, H2 blockers, Antihistamines, barbiturates, tri-cyclic antidepressants, SSRIs, etc.) using alcohol and drugs taking Simultaneous herbal medicines that affect sexual desire not willing to participate in any phase of research or not attending in more than one of the intervention sessions

Design outcomes

Primary

MeasureTime frame
Sexual desire. Timepoint: Before the intervention, immediately, 4 and 12 weeks post-intervention. Method of measurement: Persian version of the Holbert Sexuality Questionnaire (HSID).;Sexual distress. Timepoint: Before the intervention, immediately, 4 and 12 weeks post-intervention. Method of measurement: Female Sexual Distress Scale- Revised (FSDS-R).;Sexual self-disclosure. Timepoint: Before the intervention, immediately, 4 and 12 weeks post-intervention. Method of measurement: Researcher-made questionnaire.;Sexual function. Timepoint: Before the intervention, immediately, 4 and 12 weeks post-intervention. Method of measurement: Persian version of Female Sexual Function Index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRaziyeh Maasoumi

Tehran University of Medical Sciences

r_masoumi@sina.tima.ac.ir+98 21 6105 4214

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 13, 2026