sexual function. Sexual dysfunction, not caused by organic disorder or disease
Conditions
Interventions
Intervention 1: Direct counseling group:
In the intervention group, the sexual function questionnaire will be completed by participates and the sexual function score will be calculated. For consulting
Direct counseling group:
In the intervention group, the sexual function questionnaire will be completed by participates and the sexual function score will be calculated. For consulting, PLISSIT model
indirect counseling group:
In this intervention group, counseling will be done by phone and using the booklet. Before starting intervention sexual function score will be calculated. Participants will
Control group :
Before starting intervention sexual function score will be calculated.
In this group, not any counseling and special training given to individuals and only they receive routine care.
Sponsors
Vice Chancellor for Research and Technology, Kermanshah University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Inclusion criteria: infertility confirmed by specialists (both primary and secondary); having the phone (whether fixed or mobile); Having literacy; FSFI total score of sexual function by using the index as much as 26 or less; The desire to participate in the study; Availability during the next month; Having no history of abuse and use of psychotropic drugs; Lack of drug addiction; Lack of known physical and mental illness. Exclusion criteria: Not having sex during the study; Intense marital conflict (with mention of her statements); Noted abuse or sexual harassment; The occurrence of adverse event (death of loved ones, accidents with disabilities, etc.) During the last 6 months; Not wanting to continue to participate in the intervention; Inaccessibility of researcher to the samples in order to follow; Failure to respond to the questionnaire according to the person.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual function. Timepoint: Before the intervention, immediately after the intervention and four weeks after that. Method of measurement: FSFI Standard questionnaire.;Desire. Timepoint: Before the intervention, immediately after the intervention and four weeks after that. Method of measurement: FSFI Standard questionnaire.;Orgasm. Timepoint: Before the intervention, immediately after the intervention and four weeks after that. Method of measurement: FSFI Standard questionnaire.;Lubrication. Timepoint: Before the intervention, immediately after the intervention and four weeks after that. Method of measurement: FSFI Standard questionnaire.;Pain. Timepoint: Before the intervention, immediately after the intervention and four weeks after that. Method of measurement: FSFI Standard questionnaire.;Satisfaction. Timepoint: Before the intervention, immediately after the intervention and four weeks after that. Method of measurement: FSFI Standard questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSara Daeichin
Nursing & midwifery school, Kermanshah University of medical sciences.
Outcome results
None listed