ClinicalTrials.gg
CompletedNCT07220941Updated Oct 20, 2026

Digital Intervention for Adults With Misophonia

An interventional study of Acceptance and commitment therapy in Misophonia, sponsored by Utah State University. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-20.

Sponsored by Utah State University · Not applicable, Interventional, and Treatment

Updated Oct 20, 2026Now CompletedPrimary completion moved+3 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
102
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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?

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.
Read the detailed description

Misophonia, characterized by intense emotional reactions to specific sounds, significantly impacts daily functioning and quality of life. Acceptance and Commitment Therapy (ACT) has shown promise in addressing misophonia symptoms by fostering psychological flexibility. While recent intervention studies demonstrate the efficacy of ACT for misophonia, accessible and scalable treatment options remain scarce. This study aims to address this gap by developing and evaluating a fully automated, online ACT-based digital mental health intervention for misophonia. The investigators will compare the intervention to a delayed treatment group in a sample of 100 adults meeting clinical criteria for misophonia. Outcomes will include misophonia symptoms, quality of life, general distress, and psychological flexibility, assessed at baseline, mid-intervention, post-intervention, and one- and two-month follow-up. Multilevel modeling will test time by condition interactions to examine the efficacy and feasibility of an online ACT-based intervention. This fully automated online intervention aims to provide accessible, evidence-based treatment for individuals with misophonia, laying groundwork for future, larger-scale studies and public dissemination.

02

Conditions studied

  • Misophonia

Keywords

  • Acceptance and commitment therapy (ACT)
  • Digital mental health intervention (DMHI)
03

In context

Lead sponsor

Utah State University is the lead sponsor of 39 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Currently meet clinical impairment for misophonia.
  • At least 18 years old.
  • Fluent English speakers.
  • Currently live or reside in the United States

Exclusion criteria

Exclusion Criteria:

  • 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)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
102 participants (actual)

Study arms

  • Experimental
    ACT online program

    Participants will complete the 8-module fully automated digital intervention based in acceptance and commitment therapy (ACT).

    Behavioral: Acceptance and commitment therapy

  • No intervention
    Waitlist Control

    Waitlist condition; assessment only.

Interventions

  • BehavioralAcceptance and commitment therapy

    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.

    Also known as: ACT

06

What researchers measure

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).

    Time frame: 16 weeks

Secondary outcomes

  1. Misophonia acceptance and action questionnaire (Miso-AAQ; Capel et al., 2025)

    The Miso-AAQ is a 7-item self-report measure of misophonia-specific psychological inflexibility, adapted from the AAQ-III (Ong et al., 2019). Items (e.g., "I'm so afraid of my reactions to sounds that I don't do things I care about" are rated from 1 (never true) to 7 (always true) Likert scale. Total scores range from 7 to 49 with higher scores indicating greater misophonia-specific psychological inflexibility. Preliminary validation from a treatment seeking sample of adults with misophonia suggest good internal consistency and convergent validity (Capel et al., 2025).

    Time frame: 16 weeks

  2. Comprehensive assessment of Acceptance and Commitment Therapy processes (CompACT; Francis et al., 2016)

    The CompACT is a 23-item self-report measure of psychological flexibility. Items (e.g., "I make choices based on what is important to me, even if it is stressful) are rated on a 7-point Likert scale from 0 (strongly disagree) to 6 (strongly agree), with 12 items reverse-scored. Total scores range from 0 to 138 with higher scores indicating greater psychological flexibility. The CompACT demonstrates good internal consistency and convergent validity (Francis et al., 2016).

    Time frame: 16 weeks

  3. Depression Anxiety Stress Scale (DASS-21; Lovibond & Lovibond, 1995)

    The DASS-21 is a 21 item self-report measure of distress comprised of three 7-item subscales: (1) depression, (2) anxiety, and (3) stress. Items are rated from 0 (did not apply to me at all) to 3 (applied to me very much or most of the time), with higher scores indicating greater symptom severity. Subscale scores are summed and multiplied by two, yielding scores ranging from 0-42 for each subscale.

    Time frame: 16 weeks

  4. Mental Health Continuum-Short Form (MHC-SF; Keyes, 2005)

    The MHC-SF is a 14-item self-report measure of well-being. Items assess emotional, social, and psychological well-being, rated on a 6-point Likert scale from 0 (never) to 5 (every day). A total score is calculated from summing all items and ranges from 0 to 70, with higher scores reflecting greater well-being. The MHC-SF has demonstrated strong internal consistency and validity in prior studies (Lamers et al., 2011).

    Time frame: 16 weeks

Other outcomes

  1. Internalized Health-Related Stigma Scale (I-HEARTS; Pearl et al., 2024)

    The I-HEARTS is a 25-item self-report measure assessing internalized health-related stigma, adapted here to reference misophonia specifically. Items (e.g., "I am embarrassed or ashamed that I have misophonia") are rated on a 1 (strongly disagree) to 7 (strongly agree) Likert scale, with higher scores indicating greater internalized stigma. The scale yields a total score and three subscales: (1) perceived and anticipated stigma, (2) stereotype application and self-devaluation, and (3) stigma resistance (reverse-scored). Validation in a large sample of adults with chronic health conditions demonstrated strong internal consistency, test-retest reliability, and convergent validity with related constructs such as shame, loneliness, and depression (Pearl et al., 2024).

    Time frame: 16 weeks

  2. Interpersonal Reactivity Index - Perspective Taking (IRI-PT; Davis, 1980)

    The IRI-PT is a 7-item self-report subscale assessing the tendency to adopt others' psychological perspectives. Items (e.g., "Before criticizing somebody, I try to imagine how I would feel if I were in their place") are rated from 0 (does not describe me well) to 4 (describes me very well). Total scores range from 0 to 28, with higher scores indicating greater perspective-taking propensity. The IRI-PT has demonstrated good internal consistency and validity as a measure of perspective taking (Davis, 1980).

    Time frame: 16 weeks

07

Study locations

1 site
  • Utah State University
    Logan, Utah 84321, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Recruiting→Completed
changed Oct 20, 2026
Primary completion
Oct 2026→Jul 20, 2026 (actual)
Oct 20, 2026
Study completion
Feb 2027→Jul 20, 2026 (actual)
Oct 20, 2026
Enrollment
100 (estimated)→102 (actual)
Oct 20, 2026
Title
Digital Intervention for Adults With Misophonia: A Randomized Controlled Trial
Oct 20, 2026
Show all 1 update
  1. Oct 20, 2026
    Recruiting→Completed
    Primary completion Oct 2026→Jul 20, 2026 (now actual)
    Study completion Feb 2027→Jul 20, 2026 (now actual)
    Enrollment 100 (estimated)→102 (actual)
    Title Digital Intervention for Adults With Misophonia: A Randomized Controlled Trial
    + 3 other changes: description, contact details and site details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07220941
Lead sponsor
Utah State University
Collaborators
Misophonia Research Fund
Responsible party
Sponsor
First posted
Oct 24, 2025
Start date
Oct 16, 2025
Primary completion
Jul 20, 2026
Completion
Jul 20, 2026
Last update
Oct 20, 2026

Study contacts

Emily M Bowers, M.S.
principal investigator · Utah State University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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