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Clinical Trials/NCT06921187
NCT06921187Not yet recruitingNot Applicable

Etude de la Perception Auditive après Exposition PROgressive Aux Sons Aversifs Chez Des Personnes MISophonEs

Institut Pasteur2 sites in 1 country110 target enrollmentStarted: June 1, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
110
Locations
2
Primary Endpoint
score on a visual analogue scale from 0 (pleasant sound) to 10 (unpleasant sound)

Study Overview

Brief Summary

The primary objective of the project is to characterise and measure the auditory perception of subjects with misophonia compared with the auditory perception of control subjects.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •For all participants
  • •Obtain oral consent from the participant after receiving information about the study,
  • •Be 18 years or older on the day of inclusion,
  • •Be fluent in French (spoken and written),
  • •Have no known hearing loss, verified by pure tone audiometry.
  • •Declare that they do not have tinnitus,
  • •Declare that they do not have hyperacusis, verified by measuring discomfort thresholds.
  • •Be affiliated to the social security or equivalent scheme.
  • •For participants with misophonia:
  • •Declare discomfort, reduced tolerance to specific sounds (mouth noises, throat clearing, breathing, etc.).

Exclusion Criteria

  • •Bear the after-effects of an ear infection and/or have a history of an ENT disease that permanently affects hearing or balance (vestibular schwannoma, Ménière's disease, sudden or fluctuating deafness, congenital hypoacusis),
  • •Be under guardianship,
  • •deprived of liberty by judicial or administrative decision, or subject to legal protection.

Arms & Interventions

Control group

Active Comparator

Intervention: Psychoacoustic test (Behavioral)

Control group

Active Comparator

Intervention: semi-structured interviews (Other)

Misophonia group

Experimental

Intervention: Psychoacoustic test (Behavioral)

Misophonia group

Experimental

Intervention: semi-structured interviews (Other)

Misophonia group

Experimental

Intervention: Exposure to unpleasant sounds (Other)

Outcomes

Primary Outcomes

score on a visual analogue scale from 0 (pleasant sound) to 10 (unpleasant sound)

Time Frame: 1 week after enrollment

sounds will be presented at different decibels and the subject will be asked to rate the pleasantness/unpleasantness of the sound on a visual analogue scale

score on a visual analogue scale from 0 (very low intensity) to 10 (extremely intense)

Time Frame: 1 week after enrollment

sounds will be presented at different decibels and the subject will be asked to rate the intensity of the sound on a visual analogue scale

Secondary Outcomes

  • Measuring the consistency of the psychoacoustic test(1 week after enrollement)
  • the number of redundant themes in the semi-structured interviews(1 month after enrollment)
  • score on a visual analogue scale from 0 (very little discomfort) to 10 (extreme discomfort)(1 month after enrollment and 2 months after enrollment)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (2)

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