Skip to main content
Clinical Trials/NL-OMON52247
NL-OMON52247
Completed
Not Applicable

Innovative diagnostics and treatment of misophonia in children and adolescents: a new psychiatric disorder - Diagnostics and treatment of misophonia in youth.

Academisch Medisch Centrum0 sites322 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Academisch Medisch Centrum
Enrollment
322
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Eligible for participation in the healthy control group for the validation
  • study are: children between the ages of 8 and 18 years old, without
  • psychopathological symptoms of misophonia, not having received treatment for
  • misophonia in the past year. Children and their parents should have provided
  • written informed consent.
  • Eligible for participation in the patient group of the validation study and the
  • RCT study of treatment effectivity are: children between the ages of 8 and 18
  • years old, referred to the Amsterdam UMC / Levvel for diagnosis and treatment
  • of misophonia, with treatment being indicated according to clinician, parents
  • and / or child. Children and their parents should have provided written

Exclusion Criteria

  • Validation study (healthy control group): meeting the criteria for misophonia
  • on a psychopathological level, needing treatment; having had the diagnosis of
  • misophonia and / or treatment for misophonia in the past year; mental
  • retardation (estimated IQ below 85 in children and / or parents); inability to
  • read / write or understand Dutch.
  • Validation study (patient group) and RCT study of treatment effectivity: not
  • meeting the inclusion criteria; does not have misophonia as primary problem
  • domain; having psychiatric comorbid symptoms or diagnosis that hinder group
  • functioning or require change of treatment protocol\*; family problems that
  • hinder participation or adherence to treatment protocol\*; having had cognitive

Outcomes

Primary Outcomes

Not specified

Similar Trials