MedPath

The impact of cognitive-behavioral therapy on sexual function, sexual satisfaction and self- efficiency in pregnant wome

Not Applicable
Conditions
Disorder of sexual function.
lack or disorder of sexual function
Registration Number
IRCT2016111230850N1
Lead Sponsor
Vice chancellor for research, Ahvaz JundiShapur University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
32
Inclusion Criteria

have at least read and write, aged 18 to 35 years; first pregnancy; gestational age 14 to 16 weeks
Exclusion criteria: having a history of miscarriage; pregnancy complications (placenta previa threatened abortion? gestational hypertension); sexual disorder before pregnancy; use alcohol and cigarettes; drugs that affect sexual desire (such as antihypertensive drugs of antidepressants); having chronic physical and mental illnesses

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sexual self-efficacy index. Timepoint: Before the intervention, two weeks and four weeks after the intervention. Method of measurement: Schwartz sexual self-efficacy questionnaire.;Female Sexual Function Index(FSFI). Timepoint: Before the intervention, two weeks and four weeks after the intervention. Method of measurement: Female Sexual Function Questionnaire.;Sexual Satisfaction Index(ISS). Timepoint: Before the intervention, two weeks and four weeks after the intervention. Method of measurement: Larson Sexual satisfaction questionnaire.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath