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Effect of counseling based on PLISSIT model on sexual function and satisfaction in pregnant wome

Not Applicable
Conditions
Pregnancy-related condition, unspecified.
Pregnancy-related condition, unspecified
Registration Number
IRCT201505246582N14
Lead Sponsor
Vice chancellor for research, university of Tabriz medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
70
Inclusion Criteria

Inclusion Criteria:
Married women between 18 to 35 years old; Nulliparous pregnant women with gestational age of 16-20 weeks; Having documents in health-care centers in Ardabil city; Sexual performance score below 28; Literacy of reading and writing; Being monogamy

Exclusion Criteria

Prohibiting sexual activity for medical reasons (multiple pregnancy; threatened abortion; history of recurrent miscarriage; preterm delivery; severe and prolonged contractions of orgasm; incompetent cervix; the existence of placenta prevail; vaginal bleeding; premature rupture of membranes); Having known physical and mental illnesses according to self-reported (deafness or hearing impairment; mental retardation; diabetes; pre-eclampsia); Consumption of drugs affecting sexual relationships (sildenafil; antidepressants; antihistamines; diazepam’s; barbiturates; amphetamines; antihypertensive drugs, cocaine, etc.);Consumption of plant foods for increasing libido in women or men (Ginseng; cinnamon; ginger; etc.); Addiction or habitual consumption of alcohol by women; Participate in other similar studies; Occurrence of unpleasant event during the 3 months before the study (death or serious illness of close relatives).

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sexual Performance. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Sexual performance questionnaire (FSFI).
Secondary Outcome Measures
NameTimeMethod
Sexual satisfaction. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Sexual satisfaction questionnaire (LSSQ).
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