Actively Recruiting
Digital Intervention for Adults With Misophonia: A Randomized Controlled Trial
Led by Utah State University · Updated on 2025-10-24
100
Participants Needed
1
Research Sites
69 weeks
Total Duration
On this page
Sponsors
U
Utah State University
Lead Sponsor
M
Misophonia Research Fund
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to test an online intervention for adults with misophonia. The main questions it aims to answer are: 1. Is the online intervention effective, compared to a waitlist control condition? 2. Is the online intervention acceptable to use? Participants will be randomized into either the online intervention or waitlist control condition: 1. Participants in the intervention condition will be asked to complete an 8 module acceptance and commitment therapy (ACT) program for misophonia and 5 surveys over 4 months. 2. Participants in the waitlist condition will be asked to complete 5 surveys over 4 months, and will receive access to the intervention once the study is complete.
CONDITIONS
Official Title
Digital Intervention for Adults With Misophonia: A Randomized Controlled Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Currently meet clinical impairment for misophonia.
- At least 18 years old.
- Fluent English speakers.
- Currently live or reside in the United States
You will not qualify if you...
- Currently receiving alternative psychotherapy for misophonia.
- Currently modifying or starting psychotropic medication (within 30 days of starting the study).
- Any psychological and/or neurological impairments that would preclude someone from participating in the study (e.g., active self-harm or psychosis)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Utah State University
Logan, Utah, United States, 84321
Actively Recruiting
Research Team
E
Emily M Bowers, M.S.
CONTACT
M
Michael P Twohig, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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