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The effectiveness of virtual based cognitive behavioral therapy in vaginism

Effect of virtual based cognitive behavioral therapy of vaginism in Iranian women: a randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20161230031662N11
Enrollment
40
Registered
2021-08-29
Start date
2021-08-06
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

vaginismus. Counseling related to sexual attitude, behavior and orientation

Interventions

Intervention 1: The intervention consists of eight sessions composed of modules for psychoeducation, cognitive restructuring, relaxation exercises, sensate focus, attention-focusing for pain-managemen

Sponsors

Research Assistant of Alborz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Diagnosis of vaginismus based on DSM-5 by a sexologist Marital status and living with a spouse Age: 18-40 years No pregnancy Be literate Using the Internet to communicate educational counselingve sufficient Persian skills in reading and writing Have sufficient Persian skills in reading and writing

Exclusion criteria

Exclusion criteria: Psychosis or dissociative symptoms in the past or present Post Traumatic Stress Disorder(PTSD) Traumatization due tosexual abuse in the past or the present, Substance abuse or dependency in the present Moderate or severe depressionor bipolar disorder in the present Currently being treated for vaginismus Patients with physical causes leading to vaginismus Sexual dysfunction in partner Pregnancy Death of a spouse Divorce People who have not participated in the study for 2 sessions or more

Design outcomes

Primary

MeasureTime frame
Penetration. Timepoint: Before the intervention, immediately after the intervention, 4 weeks after the end of the intervention. Method of measurement: Through questionnaires.

Secondary

MeasureTime frame
Sexual function. Timepoint: Before the intervention , Immediately after the intervention, 4 weeks after the end of the intervention. Method of measurement: Rosen's sexual function Questionnaire(FSFI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaedeh Bina

Alborz University of Medical Sciences

maedehbina64@gmail.com+98 26 3419 7685

Outcome results

None listed

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