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Effectiveness of counseling pregnant women on quality of sexual life and sexual satisfaction couples in pregnancy

Phase 2
Conditions
Effectiveness of counseling pregnant women on quality of sexual life and sexual satisfaction couples in pregnancy.
sexual dysfunction, not caused by organic disorder or disease
Registration Number
IRCT2017021324469N3
Lead Sponsor
Mashhad University of Medical Sciences, Vice chancellor for research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
256
Inclusion Criteria

Inclusion criteria
Pregnant woman:
giving a written consent; having literacy; Being Iranian and living in Mashhad; Being 18 to 35 years old; Be a planned pregnancy; Has an alive singleton pregnancy; Be the first, second, third or fourth pregnancy; Does not have medical history; Does not have obstetric complications during her pregnancy or high risk pregnancy; Has’nt sexual dissatisfaction during her pregnancy.
Inclusion criteria
husband
giving a written consent; having literacy; Being Iranian and living in Mashhad; Be a planned pregnancy for her spouse; Does not have medical history; Has’nt sexual dissatisfaction during her pregnancy.
Exclusion criteria at the beginning of the study
Pregnant woman:
Current Pregnancy is after infertility treatment; Tobacco smoking, drug user, alcohol consumption or psychoactive drug; Mental problem history; happening stressful events during the past 6 months; Has experienced abortion; Takes medicine affecting on mental health; Has sexually transmitted disease; Does have vaginal intercourse due to hit in pelvic area or penis deformity.
Exclusion criteria during the study
Pregnant woman:
Lack of tendency of pregnant woman to continue her cooperation; Incomplete questionnaires; Be admitted to the hospital due to problems related to pregnancy during the study; Occur stressful event during the study; Be inaccessible in the second and the fourth week after consultation; Questionnaire is not filled in by the spouse of the pregnant woman.
Exclusion criteria at the beginning of the study
Husband
Tobacco smoking, drug user, alcohol consumption or psychoactive drug; Mental problem history; happening stressful events during the past 6 months; Takes medicine affecting on mental health; Has sexually transmitted disease; Taking medications effecting sexual function; Does have vaginal intercourse due to hit in pelvic area or penis deformity.
Exclusion criteria during the study
Husband
Lack of tendency to continue his cooperation; Incomplete questionnaires; Occur stressful event during the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sexual satisfaction. Timepoint: Before the intervention and 2 and 4 weeks after begining of intervention. Method of measurement: Larson sexual satisfaction questionnaire (LSSQ).;Quality of sexual life. Timepoint: Before the intervention and 2 and 4 weeks after begining of intervention. Method of measurement: Quality of sexual life questionnaire (SQOL).
Secondary Outcome Measures
NameTimeMethod
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