Digital Intervention for Adults With Misophonia: A Randomized Controlled Trial
Efficacy and Feasibility of an Online Acceptance Based Intervention for Misophonia: A Randomized Controlled Trial
1 other identifier
interventional
100
1 country
1
Brief Summary
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?
- 3.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.
- 4.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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2025
CompletedFirst Submitted
Initial submission to the registry
October 21, 2025
CompletedFirst Posted
Study publicly available on registry
October 24, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 1, 2027
October 24, 2025
October 1, 2025
1 year
October 21, 2025
October 21, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Selective Sound Sensitivity Syndrome Scale (S-Five; Vitoratou et al., 2021)
The S-Five is a 25-item self-report measure of misophonia severity. Items (e.g., "I feel trapped if I cannot get away from certain noises") are rated on a 0 (not at all true) to 10 (completely true) ordinal scale with total scores ranging from 0 to 250. The S-Five consists of five latent factors: (1) externalizing appraisals (e.g., blaming others for making sounds), (2) internalizing appraisals (e.g., negative self-judgments triggered by misophonia), (3) impact on functioning (e.g., social and occupational impact), (4) outburst (e.g., experiences of aggression or fear of losing control), and (5) threat (e.g., feeling trapped or helpless). The S-Five demonstrates good internal consistency and convergent validity with other misophonia measures (Vitoratou et al., 2023).
16 weeks
Secondary Outcomes (4)
Misophonia acceptance and action questionnaire (Miso-AAQ; Capel et al., 2025)
16 weeks
Comprehensive assessment of Acceptance and Commitment Therapy processes (CompACT; Francis et al., 2016)
16 weeks
Depression Anxiety Stress Scale (DASS-21; Lovibond & Lovibond, 1995)
16 weeks
Mental Health Continuum-Short Form (MHC-SF; Keyes, 2005)
16 weeks
Other Outcomes (2)
Internalized Health-Related Stigma Scale (I-HEARTS; Pearl et al., 2024)
16 weeks
Interpersonal Reactivity Index - Perspective Taking (IRI-PT; Davis, 1980)
16 weeks
Study Arms (2)
ACT online program
EXPERIMENTALParticipants will complete the 8-module fully automated digital intervention based in acceptance and commitment therapy (ACT).
Waitlist Control
NO INTERVENTIONWaitlist condition; assessment only.
Interventions
Participants will complete the 8-module fully automated digital intervention based in acceptance and commitment therapy (ACT). The digital program is based off of an ACT protocol developed in a prior randomized controlled trial and adapted for digital self-help use (Bowers et al., 2024). Modules focus on focus on acceptance, cognitive defusion, present moment awareness, values clarification, and functional adaptations.
Eligibility Criteria
You may qualify if:
- Currently meet clinical impairment for misophonia.
- At least 18 years old.
- Fluent English speakers.
- Currently live or reside in the United States
You may not qualify if:
- 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)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Utah State Universitylead
- Misophonia Research Fundcollaborator
Study Sites (1)
Utah State University
Logan, Utah, 84321, United States
MeSH Terms
Conditions
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Emily M Bowers, M.S.
Utah State University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 21, 2025
First Posted
October 24, 2025
Study Start
October 1, 2025
Primary Completion (Estimated)
October 1, 2026
Study Completion (Estimated)
February 1, 2027
Last Updated
October 24, 2025
Record last verified: 2025-10
Data Sharing
- IPD Sharing
- Will not share