A Comparative study of direct and indirect counseling on sexual function of infertile women referring to infertility clinic of Kermanshah Motazedi hospital

Not Applicable

• Conditions: sexual function.; Sexual dysfunction, not caused by organic disorder or disease

• Registration Number: IRCT2016052928162N1
• Lead Sponsor: Vice Chancellor for Research and Technology, Kermanshah University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 60

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

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.