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Clinical Trial Summary

The purpose of this study is to determine the feasibility of administering auricular acupressure for patients with interstitial cystitis/bladder pain syndrome (IC/BPS), and evaluating the efficacy of auricular acupressure to reduce pain scores and decrease pain medication usage over time.


Clinical Trial Description

Eligible participants will be asked to complete baseline questionnaires. After completion, a study interventionist will place 10 adhesive acupressure pads/seeds on the participant's ears (5 on each ear). Each seed will be placed on a specific site on the ear believed to help with pain and overall well-being. Over the course of 5 days, participants will be asked to apply a small amount of manual pressure with their fingers to each of the ear pads and answer daily study questionnaires. This feasibility trial is being conducted in collaboration with the Battlefield Auricular Acupressure (BAApress) Training and Intervention Fidelity study (IRB00084011). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05857020
Study type Interventional
Source Wake Forest University Health Sciences
Contact Stephen Walker, PhD
Phone 336-713-7272
Email swalker@wakehealth.edu
Status Not yet recruiting
Phase N/A
Start date July 2024
Completion date October 2025

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