Sexual dysfunction. Sexual dysfunction, not caused by organic disorder or disease
Conditions
Interventions
Intervention 1: The experimental group-A: will receive consultation based on PLISSIT model (Permission-limited Information-Specific Suggestion-Intensive Therapy) by a trained midwife during 4 weeks t
Behavior
The experimental group-A: will receive consultation based on PLISSIT model (Permission-limited Information-Specific Suggestion-Intensive Therapy) by a trained midwife during 4 weeks that in each week
The control group: will receive routine sexual consultation.
The experimental groups-B: will receive personal consultation during 4 weeks that in each week one session will be conducted.
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Inclusion criteria: women who are married, do not suffer from any other chronic disease, and have sexual problems (FSFI score<28). they should have sexual relationship with their husband. Exclusion criteria: If a woman does not want to continue take parting in this study or becomes pregnant or does not come to all sessions of intervention, she will be omitted.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual function. Timepoint: Before the intervention; two monthes and three monthes after intervention. Method of measurement: Female Sexual Function Index questionnare. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life. Timepoint: Two monthes and three monthes after intervention. Method of measurement: SF36 questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Daneshfar
Tehran University of Medical Sciences
Outcome results
None listed