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

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

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00007482

Enrollment

Registered

2018-07-19

Start date

2014-11-15

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

F51.0 F51.5

Interventions

Group 1: Experimental-Condition: Group-intervention for children and their parents. Children 5-11 years suffering from insomnia and/or nightmares are included. The group-treatment is manualized, based

Eligibility

Sex/Gender

All

Age

5 Years to 11 Years

Inclusion criteria

Inclusion criteria: insomnia, nightmares

Exclusion criteria

Exclusion criteria: intellectual retardation

Design outcomes

Primary

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

Secondary

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

Countries

Germany

Contacts

Public ContactAngelika Schlarb

Bielefeld University

angelika.schlarb@uni-bielefeld.de+49 521 106-4320

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026