Factors Influencing Selective Mutism

NCT ID: NCT04233905

Last Updated: 2020-01-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

92 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-08-01

Study Completion Date

2019-07-31

Brief Summary

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The study's goal is to check and verify basic assumptions of a new selective mutism developmental model from Melfsen and Walitza through standardized and routinely used patient questionnaires. The primary emphasis is the question of a connection between selective mutism and high sensitivity, dissociation, emotional regulation, family structure, social anxiety and self-esteem.

Detailed Description

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Conditions

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Selective Mutism

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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mute children

mute children and their mothers

Psychometric questionnaire study

Intervention Type BEHAVIORAL

Four groups participate in the psychometric questionnaire study. A group of mute children and their mothers (EG:A), as well as a normal, healthy control group (KG:A) with roughly the same age and sex characteristics fill out one-time questionnaires about current daily life experiences. In addition, another group of formerly mute adults (EG:B) as well as a comparable age/sex normal control group will be retrospectively questioned using the same specifically tailored questionnaire.

healthy children

healthy children control group

Psychometric questionnaire study

Intervention Type BEHAVIORAL

Four groups participate in the psychometric questionnaire study. A group of mute children and their mothers (EG:A), as well as a normal, healthy control group (KG:A) with roughly the same age and sex characteristics fill out one-time questionnaires about current daily life experiences. In addition, another group of formerly mute adults (EG:B) as well as a comparable age/sex normal control group will be retrospectively questioned using the same specifically tailored questionnaire.

mute adults

formerly mute adults

Psychometric questionnaire study

Intervention Type BEHAVIORAL

Four groups participate in the psychometric questionnaire study. A group of mute children and their mothers (EG:A), as well as a normal, healthy control group (KG:A) with roughly the same age and sex characteristics fill out one-time questionnaires about current daily life experiences. In addition, another group of formerly mute adults (EG:B) as well as a comparable age/sex normal control group will be retrospectively questioned using the same specifically tailored questionnaire.

healthy adults

healthy adults control group

Psychometric questionnaire study

Intervention Type BEHAVIORAL

Four groups participate in the psychometric questionnaire study. A group of mute children and their mothers (EG:A), as well as a normal, healthy control group (KG:A) with roughly the same age and sex characteristics fill out one-time questionnaires about current daily life experiences. In addition, another group of formerly mute adults (EG:B) as well as a comparable age/sex normal control group will be retrospectively questioned using the same specifically tailored questionnaire.

Interventions

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Psychometric questionnaire study

Four groups participate in the psychometric questionnaire study. A group of mute children and their mothers (EG:A), as well as a normal, healthy control group (KG:A) with roughly the same age and sex characteristics fill out one-time questionnaires about current daily life experiences. In addition, another group of formerly mute adults (EG:B) as well as a comparable age/sex normal control group will be retrospectively questioned using the same specifically tailored questionnaire.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Children and young people from 8-18 years of age who fulfill the international classification of diseases tenth edition (ICD-10) for selective mutism
* Adults who suffered selective mutism when they were children or adolescents
* All study participants or their legal representative have given written permission for their experiences to be documented in the study.

Exclusion Criteria

* Temporary mutism, e.g. from emotional disturbances or separation anxiety (F93.0), or depression
* Profound developmental disturbances (F84.2) like early childhood autism (F84.0), atypical autism (F84.1), Rett Syndrome (F84.2), alternative disintegrative childhood disturbances (F84.3), hyperactivity disturbance with decrease of intelligence and movement stereotypes (F84.5), or Asperger's Syndrome.
* Schizophrenia (F20)
* Profound mental retardation
* Delineated development disturbances of speech and language (F80)
* Organic brain disease with loss of language or disturbance of speech development
Minimum Eligible Age

8 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Susanne Walitza

OTHER

Sponsor Role lead

Responsible Party

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Susanne Walitza

Head of the Department of Child and Adolescent Psychiatry

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Susanne Walitza, Prof. Dr. med. Dipl.-Psych.

Role: PRINCIPAL_INVESTIGATOR

Sponsor-Investigator

Locations

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Psychiatric University Clinics, Department of Child and Adolescent Psychiatry

Zurich, Canton of Zurich, Switzerland

Site Status

Countries

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Switzerland

References

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Melfsen S, Jans T, Romanos M, Walitza S. Emotion regulation in selective mutism: A comparison group study in children and adolescents with selective mutism. J Psychiatr Res. 2022 Jul;151:710-715. doi: 10.1016/j.jpsychires.2022.05.040. Epub 2022 May 24.

Reference Type DERIVED
PMID: 35690008 (View on PubMed)

Melfsen S, Romanos M, Jans T, Walitza S. Betrayed by the nervous system: a comparison group study to investigate the 'unsafe world' model of selective mutism. J Neural Transm (Vienna). 2021 Sep;128(9):1433-1443. doi: 10.1007/s00702-021-02404-1. Epub 2021 Aug 14.

Reference Type DERIVED
PMID: 34390394 (View on PubMed)

Other Identifiers

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KJPP 2017-00679

Identifier Type: -

Identifier Source: org_study_id

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