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The impact of consulting on satisfaction and sexual function of pregnant wome

Phase 2
Conditions
Consulting relationship to satisfaction and sexual function.
Lack or loss of sexual desire
Registration Number
IRCT2015070713405N11
Lead Sponsor
Vice chancellor for Research and Technology, Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
80
Inclusion Criteria

Inclusion criteria include: The age range 18-35 years; single fetus and gestational age 24-26 weeks; lack of mental disorders according to psychiatrist
; not having gestational diabetes melitus, preeclampcia, bleeding, premature rupture of membranes; not taking sedative drugs; having sexual dysfunction confirmed by a psychiatrist; not having a history of having sexual dysfunction before pregnancy; exclusively female sexual dysfunction confirmed by psychiatrist. Exclusion criteria includes: occuring any problem in pregnancy during study (abruption, fetal abnormal situation, cord prolapse, bleeding, diabetes, hypertension, preterm labor); abnormal pattern of fetal heart rate or decrease of fetal movements that require medical intervention.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sexual satisfaction. Timepoint: Before intervention; 2 weeks after intervention; 4 weeks after intervention. Method of measurement: Lindaberg Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Sextual function. Timepoint: Before intervention; 2 weeks after intervention; 4 weeks after intervention. Method of measurement: FSFI Questionnaire.
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