Skip to content

The impact of cognitive-behavioral therapy on sexual function, sexual satisfaction and self- efficiency in pregnant women

The impact of cognitive-behavioral therapy on sexual function, sexual satisfaction and self- efficiency in Nulliparous pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016111230850N1
Enrollment
32
Registered
2017-01-24
Start date
2016-12-05
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

Disorder of sexual function. lack or disorder of sexual function

Interventions

Intervention 1: Consultations are done a week for 8 sessions of 45-minute sessions on an individual basis and Each session has a specific structure. Intervention 2: The control group only received pre
Behavior
Consultations are done a week for 8 sessions of 45-minute sessions on an individual basis and Each session has a specific structure

Sponsors

Vice chancellor for research, Ahvaz JundiShapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: have at least read and write, aged 18 to 35 years; first pregnancy; gestational age 14 to 16 weeks Exclusion criteria: having a history of miscarriage; pregnancy complications (placenta previa threatened abortion? gestational hypertension); sexual disorder before pregnancy; use alcohol and cigarettes; drugs that affect sexual desire (such as antihypertensive drugs of antidepressants); having chronic physical and mental illnesses

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sexual self-efficacy index. Timepoint: Before the intervention, two weeks and four weeks after the intervention. Method of measurement: Schwartz sexual self-efficacy questionnaire.;Female Sexual Function Index(FSFI). Timepoint: Before the intervention, two weeks and four weeks after the intervention. Method of measurement: Female Sexual Function Questionnaire.;Sexual Satisfaction Index(ISS). Timepoint: Before the intervention, two weeks and four weeks after the intervention. Method of measurement: Larson Sexual satisfaction questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMina Nezamnia

Ahvaz Jundishapur University of Medical Sciences

Minanezamnia@gmail.com+98 61 3336 7543

Outcome results

None listed

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