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

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

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017021324469N3
Enrollment
256
Registered
2017-03-08
Start date
2016-07-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

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

Interventions

Intervention 1: Before intervention, Quality of sexual life (SQOL-F) and sexual satisfaction questionnaire(LSSQ) will be filled in by intervention group. two sessions (60 to 90 minutes) will be held b
Behavior
Routine care consultation will be provided for control group
Before intervention, Quality of sexual life (SQOL-F) and sexual satisfaction questionnaire(LSSQ) will be filled in by intervention group. two sessions (60 to 90 minutes) will be held by a midwife rese

Sponsors

Mashhad University of Medical Sciences, Vice chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNajmeh Dehlari

School of Nursing and Midwifery

dehlarin921@mums.ac.ir+95 5138477339

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026