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Cognitive behavioral therapy for Misophonia, RCT

Cognitive behavioral therapy for Misophonia, RCT - Cognitive behavioral therapy for Misophonia, RCT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON43118
Enrollment
64
Registered
2017-01-23
Start date
2017-02-23
Completion date
Unknown
Last updated
2025-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

anger/disgust of noise Misophonia

Interventions

Cognitive Therapy (CT), attention training and applied relaxation. Subjects will take part in our treatment program, which was especially developed for treating patients with misophonia. The program

Sponsors

AMC Psychiatrie
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Misophonia, Impuls control disorder NOS

Exclusion criteria

Exclusion criteria: Presence of any of the following DSM-IV-TR conditions: -Major depression -Major anxiety disorder -Bipolar disorder -Autism spectrum disorders -Schizophrenia or any other psychotic disorder -Substance related disorder during the past 6 months -Any structural CNS disorder or stroke within the last year

Design outcomes

Primary

MeasureTime frame
Our primary outcome measure will constitute of misophonia symptom severity as measured by the AMisoS-R (Schröder et al. in press).

Secondary

MeasureTime frame
Our secondary study parameters will focus on daily psychosocial functioning and quality of life. The Dutch versions of the following rating scales will be used to asses psychosocial functioning: the Sheehan Disability Scale (SDS, Sheehan, 1983) and the Symptom Checklist-90-R (SCL-90R, Derogatis, 1973). Quality of life will be measured by the Euro Quality of life 6 Dimensions (EQ-6D, The EuroQol Group. (2011)and the WHO Quality of Life-BREF (WHOQOL-BREF, WHOQOL group. Development of the World Health Organization WHOQOL-BREF quality of life assessment. The WHOQOL Group. Psychol Med 1998;28:551-8.)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)