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Clinical Trial Summary

Given the high rates and associated impairment of sexual concerns during the menopausal transition, and specifically during perimenopause, our team has developed a CBT protocol specifically designed to target these prevalent and distressing sexual concerns. The broad aim of the proposed study is to validate this new protocol in a clinic that provides empirically-supported assessment and intervention services for women with menopause-related symptoms. The primary objective of this study is to evaluate the efficacy of a four-week individual CBT protocol in improving sexual satisfaction and reducing distress during perimenopause. The secondary objective of this study is to evaluate the efficacy of this CBT protocol to improve sexual functioning (e.g., desire, arousal), relationship satisfaction, and body image. Exploratory analyses will examine the impact on this CBT protocol on vasomotor symptoms, depression, and anxiety.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04922385
Study type Interventional
Source St. Joseph's Healthcare Hamilton
Contact Sheryl M Green, PhD, CPsych
Phone 905-522-1155
Email sgreen@stjoes.ca
Status Recruiting
Phase N/A
Start date January 1, 2021
Completion date March 31, 2023

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