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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201505246582N14
Enrollment
70
Registered
2017-06-26
Start date
2017-04-21
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

Pregnancy-related condition, unspecified. Pregnancy-related condition, unspecified

Interventions

Intervention 1: In the intervention group, sex counseling based on PLISSIT model will be given singularly during meetings with 45-60 min duration, once a week for consecutive weeks according to part
Behavior
In the intervention group, sex counseling based on PLISSIT model will be given singularly during meetings with 45-60 min duration, once a week for consecutive weeks according to participants needs.
control group: will receive routine prenatal care.

Sponsors

Vice chancellor for research, university of Tabriz medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

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).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sexual Performance. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Sexual performance questionnaire (FSFI).

Secondary

MeasureTime frame
Sexual satisfaction. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Sexual satisfaction questionnaire (LSSQ).

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmahin kamalifard

Tabriz University Of Medical Sciences

kamalifardm@tbzmed.ac.ir+98 41 3479 6770

Outcome results

None listed

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