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Examining the Effectiveness of a Group Cognitive-behavioural Treatment Program for Persistent Genital Arousal Disorder

Persistent Genital Arousal Disorder

This study seeks to provide information regarding the effectiveness of a virtual, synchronous cognitive behavioural therapy (CBT) group program for women with Persistent Genital Arousal Disorder/Genitopelvic Dysesthesia (PGAD/GPD). The program consists of 8 weekly sessions of two hours each, which focus on education and understanding, and learning skills and strategies to manage PGAD/GPD symptoms, and related mental health and lifestyle impacts, as well as structured opportunities for discussion and shared reflection. The group therapy program involves elements based in Cognitive Behavioural Therapy (CBT), Acceptance and Commitment Therapy (ACT), and Dialectical Behaviour Therapy (DBT). Participants in the present study will provide responses to online surveys (before, during, and immediately after treatment, also 3 and 6 months after treatment) regarding their PGAD/GPD symptoms, mental health symptoms, and sexual wellness (sexual pleasure and distress).

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Participation Requirements

  • Sex:

    ALL

  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* at least 18 years of age
* fluent in English
* have a physician-based diagnosis of PGAD/GPD
* reside in Ontario, Canada
* be comfortable answering questions about their health (mental and physical) and sexuality in online surveys
* be comfortable discussing their mental and physical health and PGAD/GPD symptoms in group online therapy sessions with video on

Exclusion Criteria:

* under the age of 18 years
* nonfluent in English
* lack of physician based diagnosis of PGAD/GPD
* not comfortable with answering questions about mental, physical, sexual health
* not comfortable with discussing mental and physical health and PGAD/GPD symptoms in group online therapy sessions with video on
* mental or physical health conditions that preclude involvement in group therapy

Study Location

Sexual Health Research Laboratory, Department of Psychology, Queen's University
Sexual Health Research Laboratory, Department of Psychology, Queen's University
Kingston, Ontario
Canada

Contact Study Team

Backup Contact

Shannon Coyle, MA

[email protected]
613 533 3276
Primary Contact

Caroline Pukall, PhD

[email protected]
613 533 3200
Study Sponsored By
Queen's University
Participants Required
More Information
Study ID: NCT05919784