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Evaluation of a new rehabilitation concept for children and adolescents with child and adolescent psychiatric disorders with a focus on participation impairment

Evaluation of a new rehabilitation concept for children and adolescents with child and adolescent psychiatric disorders with a focus on participation impairment

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
DRKS
Registry ID
DRKS00022239
Enrollment
400
Registered
2020-06-18
Start date
2020-08-18
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

F20 F32.1 F33 F40 F41 F42 F43.1 F44 F90 F91 F92 F94.1

Interventions

Group 1: Intervention group - rehabilitation according to a new treatment concept (approx. 4-6 weeks of inpatient rehabilitation, the contents of which were developed age-specifically on S3 guidelines

Sponsors

Institut für rehabilitationsmedizinische Forschung an der Universität Ulm
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 18 Years

Inclusion criteria

Inclusion criteria: Children and adolescents with the following ICD-10 F diagnoses (also possible as secondary diagnosis): - F20 Schizophrenia - F90 ADHD / hyperkinetic disorder - F91 Conduct disorders - F92 Mixed disorders of conduct and emotions - F94.1 ff (Reactive) attachment disorder of childhood - F32.1 ff moderate depressive episodes - F33 recurrent depressive disorder - F40/41 anxiety and phobic disorders - F42 Obsessive-compulsive disorder - F43.1 Post-traumatic stress disorder - F44 Dissociative disorders; Sufficient communication skills in German (patients of at least 11 years are queried via self-survey, patients under 11 years of age are questioned via external survey by their caregiver who needs sufficient knowledge of the German language); Rehabilitation payed by the DRV-BW

Exclusion criteria

Exclusion criteria: Insufficient knowledge of the German language; Children and adolescents with certain other diagnoses that occur in addition to one or more of the above-mentioned ICD-10 F diagnoses: - Dependence syndrome (F1x.2) - Personality disorder from F60 - F63, excluding F63.3 and F63.8 - early childhood developmental disorder (F84.0, F84.2, F84.4, excl. F84.5) and mental retardation; Highly intensive individual therapeutic work, continuous 1:1 care, acute need for treatment as well as acute self- and/or external danger; Control group: Participation in ADHD training from May 2018 during their rehabilitation stay between May and October 2018, as this was already implemented in standardized form from the new treatment concept as a test run.

Design outcomes

Primary

MeasureTime frame
The ability to participate in school as the primary target criterion. Measurement is based on a questionnaire survey (self and/or external survey), in which, among other things, the measuring instruments KINDL and parts of the SDQ are used. Intervention group: - Survey at the beginning of rehabilitation (t1) - Survey at the end of rehabilitation (t2) - Follow-up survey two years after rehabilitation (t3) Control group: - Follow-up survey two years after rehabilitation (t3) In addition, a secondary data evaluation of selected routinely collected case data (e.g. parts of the discharge report) of all participating children and adolescents is carried out.

Secondary

MeasureTime frame
Health status, quality of life and life satisfaction, disease management, expectations of the rehabilitation program, subjective prognosis and treatment success as well as satisfaction with the rehabilitation treatment and the treatment process are to be defined as secondary objectives. These are also collected via questionnaire surveys of the intervention and control group and on the basis of routinely collected case data (see primary endpoint for further details) as well as via qualitative interviews with treating specialists at the rehabilitation clinic.

Countries

Germany

Contacts

Public ContactSarah Leinberger

Institut für rehabilitationsmedizinische Forschung an der Universität Ulm

sarah.leinberger@ifr-ulm.de07582-8005108

Outcome results

None listed

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