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A pilot randomized control trial to determine the feasibility of a hypnosis intervention for the treatment of bladder pain syndrome/interstitial cystitis.

A pilot randomized control trial to determine the feasibility of a hypnosis intervention for the treatment of bladder pain syndrome/interstitial cystitis.

Enrolling By Invitation
18-80 years
All
Phase N/A
The expected duration of your involvement in this research study will be up to 3 months from the time of enrollment. The intervention for this study will be 3 in person hypnosis sessions over 3 weeks plus a mobile web application for use of at least 2 times per week between the in-person hypnosis sessions. The mobile hypnosis application will be continued for 3 months after the in-person intervention. A follow up questionnaire will be administered at one month and two months after the first in-person hypnosis session. For those subjects randomized to the hypnosis group, a magnetic resonance imaging (MRI) study will be performed between the 1 month and 3 month follow up visits. The total duration of the study is 24 months. The total number of subjects in this study will be 30 patients with bladder pain syndrome.
Study details
    cystitis
    bladder

TX6320

19 February 2024

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