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Efficacy of Cognitive Behavioral Therapy on women with vaginismus

Efficacy of Cognitive Behavioral Therapy on women with vaginismus: A Replicated Single-Case Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015110724922N1
Enrollment
4
Registered
2016-06-20
Start date
2015-06-05
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

vaginismus. psychogenic vaginismus

Interventions

The present study is a replicated single-case design which evaluates the effect of CBT for lifelong vaginismus. Participants are 4 women with vaginismus that completed a demographic and multidimension
Behavior

Sponsors

Vice Chancellor for Research of Ahvaz Jundishapur University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Lifelong vaginismus (unconsummated marriage) 2.the ability of reading and writing at least 3.women between 18 to 35 years old exclusion criteria: 1.Patient with physical causes of vaginismus according to the gynecologist or midwife's diagnosis 2. Acute or chronic physical disease 3. Mental illness confirmed by psychiatric 4.Addiction to drugs or alcohol 5- have a Partner with any kind of sexual dysfunction

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Penetration. Timepoint: End intervention. Method of measurement: Report person.

Secondary

MeasureTime frame
Genital conflict. Timepoint: Before intervention, second session, fourth session, sixth session, eighth session,three follow up two months after intervention with twenty day interval. Method of measurement: Multi dimensional vaginal penetration Questionnaire.;Terrible thoughts and contraction. Timepoint: Before intervention, second session, fourth session, sixth session, eighth session,three follow up two months after intervention with twenty day interval. Method of measurement: Multi dimensional vaginal penetration Questionnaire.;Helplessness. Timepoint: Before intervention, second session, fourth session, sixth session, eighth session,three follow up two months after intervention with twenty day interval. Method of measurement: Multi dimensional vaginal penetration Questionnaire.;Marital adjustment. Timepoint: Before intervention, second session, fourth session, sixth session, eighth session,three follow up two months after intervention with twenty day interval. Method of measurement: Multi dimensional vaginal penetration Questionnaire.;Shirk. Timepoint: Before intervention, second session, fourth session, sixth session, eighth session,three follow up two months after intervention with twenty day interval. Method of measurement: Multi dimensional vaginal penetration Questionnaire.;Impetus. Timepoint: Before intervention, second session, fourth session, sixth session, eighth session,three follow up two months after intervention with twenty day interval. Method of measurement: Mult idimensiona lvaginal penetration Questionnaire.;Sexual Information. Timepoint: Before intervention, second session, fourth session, sixth session, eighth session,three follow up two months after intervention with twenty day interval. Method of measurement: Multi dimensional vaginal penetration Questionnaire.;Hypervigilant. Timepoint: Before intervention, second session, fourth session, sixth session, eighth session,three follow up two months after intervention with twenty day interval. Me

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArezoo Rezaei KheyrAbady

Ahvaz Jundyshapur University of Medical Sciences

arezoo.rezaei66@gmail.com , rezaei.a@ajums.ac.ir+98 61 3373 8071

Outcome results

None listed

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