Efficacy of a multimodal group-training for children with insomnia - a randomized control study with 3 months follow-up

Not Applicable

• Conditions: F51.0; F51.5; Nonorganic insomnia; Nightmares

• Registration Number: DRKS00007482
• Lead Sponsor: Bielefeld University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-07-19
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 117

Inclusion Criteria

insomnia, nightmares

Exclusion Criteria

intellectual retardation

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
a) Reduction of sleep onset latency 3 months after treatment (based on actigraphy)<br>b) insomnia symptoms 3 months after treatment.<br>Methods:<br>Schlaf-diary<br>Children Sleep Habits Questionnaire<br>Sleep Self Report<br>Children Sleep Comic<br>Aktigraphy<br>

Secondary Outcome Measures

Name	Time	Method
3 months after treatment:<br>A) remission rate regarding sleep disorder (insomnia/nightmares) based on ICSD-3 criteria.<br>B) significant improvement of mental health measured by Child Behavior Checklist.<br>C) parents suffer significant less from mental stress (SCL-90)<br>