female sexual dysfunction. other sexual dysfunction, not caused by organic disorder or disease
Conditions
Interventions
Intervention 1: Treatment with 50 mg sildenafil orally one hour before intercourse. Intervention 2: Cognitive-behavioral therapy weekly for 8 sessions was conducted by a female therapist with a PhD in
Treatment - Drugs
Behavior
Treatment with 50 mg sildenafil orally one hour before intercourse
Cognitive-behavioral therapy weekly for 8 sessions was conducted by a female therapist with a PhD in clinical psychology according to the following protocol: from the first to the third session: Intro
Sponsors
Vice Chancellor for research, Kashan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 45 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Being in a monogamous relationship with only one guy for at least 6 months prior to participation in the study; The presence of sexual functioning disorders diagnosed by a psychiatrist. Exclusion criteria: symptomatic heart diseases; untreated psychiatric disorders; spinal cord injuries; uncontrolled diabetes mellitus; history of drug abuse; alcohol use; stroke during at least the six previous months; heart attack during at least the six previous months; physical problems of female reproductive tract diagnosed by the gynecologist; those who do not have the willingness to have sex due to familial conflicts
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual desire. Timepoint: before the intervention/4weeks after the intervention/8weeks after the intervention/12weeks after the intervention(end of intervention). Method of measurement: FSFI standardized questionnaire.;Sexual excitment. Timepoint: before the intervention/4weeks after the intervention/8weeks after the intervention/12weeks after the intervention(end of intervention). Method of measurement: FSFI standardized questionnaire.;Vaginal lubrication. Timepoint: before the intervention/4weeks after the intervention/8weeks after the intervention/12weeks after the intervention(end of intervention). Method of measurement: FSFI standardized questionnaire.;Orgasm. Timepoint: before the intervention/4weeks after the intervention/8weeks after the intervention/12weeks after the intervention(end of intervention). Method of measurement: FSFI standardized questionnaire.;Sexual satisfaction. Timepoint: before the intervention/4weeks after the intervention/8weeks after the intervention/12weeks after the intervention(end of intervention). Method of measurement: FSFI standardized questionnaire.;Dysparonia. Timepoint: before the intervention/4weeks after the intervention/8weeks after the intervention/12weeks after the intervention(end of intervention). Method of measurement: FSFI standardized questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr.Fatemeh Mehrzad
Kashan University of Medical Sciences
Outcome results
None listed