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Efficacy of Internet Based Parent Management Training in the Treatment of Afective Dysregulation and Coexisting Conditions in Children

Efficacy of Internet Based Parent Management Training in the Treatment of Afective Dysregulation and Coexisting Conditions in Children - ADOPT online

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00014963
Enrollment
200
Registered
2018-06-27
Start date
2018-07-09
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

mood dysregulation as transdiagnostic dimension F34.8

Interventions

Group 1: Intervention group: online parent training at least one hour weekly for 12 weeks Group 2: Treatment as usual: Parents of this group are advised to search for a psychosocial support if wanted

Sponsors

Universität zu Köln Humanwissenschaftliche Fakultät Psychologie und Psychotherapie in Heilpädagogik und Rehabilitation
Lead Sponsor

Eligibility

Sex/Gender
All
Age
107 Months to 155 Months

Inclusion criteria

Inclusion criteria: - Age 8;0 to 12;11 yrs. - Resident with at least one natural or adoptive parent - Clinician-rated Outcome Measure for AD (DADYS interview, DADYS questionnaire) > cut-off. The cut-off will be determined by a clinical overall rating of AD at the end of the structured clinical parent interview. - Willingness and ability of parents to participate in the online intervention (existence of an informed consent of the guardians and an assent of the child) - Sufficient knowledge of German language

Exclusion criteria

Exclusion criteria: - Intelligence <80 (visit to a special school for mental development or to a regular school with funding priority mental development) - Resident without natural or adoptive parents (e.g. foster parents, grandparents) - mental disorder other than Coexisting Conditions (CoCo) is primary disorder and main cause of AD (e.g. autism spectrum disorder) - current or planned intensive behavioral therapy on a weekly/biweekly basis

Design outcomes

Secondary

MeasureTime frame
(1) psychosocial impairment of the child due to AD symptoms based on patient and parent interview (DADYS interview/DADYS questionnaire) (2) patient- and parent-rated AD symptoms of the child (DADYS questionnaire) (3) patient- and parent-rated symptoms of ADHD and ODD/CD (SBB-ADHS/-SSV, FBB-ADHS/-SSV) (4) other comorbid conditions (e.g., anxiety, depression) assessed by parent-ratings (CBCL 6-18R) (5) psychological well-being in patient- and parent-rating (KIDSCREEN-27) (6) parental satisfaction with the treatment (self-developed questionnaire) (1)-(5) will be collected at T1-T4; (6) will be collected at T2

Primary

MeasureTime frame
Blinded clinician-rated AD (=Affective Dysregulation) symptom score of the child, assessed with a newly developed outcome measure for AD (DADYS interview) based on patient and parent interview at T1-T4

Countries

Germany

Contacts

Public ContactAnne Ritschel

Universität zu Köln Humanwissenschaftliche Fakultät Psychologie und Psychotherapie in Heilpädagogik und Rehabilitation

adopt-studie@uni-koeln.de022147076181

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 2, 2026