- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06011642
Reliability and Validity of a Digital Version of a Structured Interview for Children and Adolescents (Kinder-eDIPS)
June 3, 2025 updated by: Ruth von Brachel, Ruhr University of Bochum
Reliability, Validity and Acceptance of the Kinder-eDIPS (Diagnostisches Interview Bei Psychischen Störungen im Kindes- Und Jugendalter)
The Kinder-eDIPS is a digital version of the Kinder-DIPS (Diagnostisches Interview bei Psychischen Störungen im Kindes- und Jugendalter), a structured interview to assess a variety of the most frequent psychological disorders in children and adolescents.
In this study, the reliability, validity and acceptance of the Kinder-eDIPS will be tested in both a clinical and a non-clinical sample.
Study Overview
Status
Completed
Conditions
Detailed Description
The Kinder-eDIPS is a digital version of the Kinder-DIPS (Diagnostisches Interview bei Psychischen Störungen im Kindes- und Jugendalter), a structured interview to assess a variety of the most frequent psychological disorders in children and adolescents.
The interview is administered by trained clinicians with children/adolescents and one of their primary carers.
The reliability, validity and acceptance of former versions of the Kinder-DIPS (Kinder-DIPS for DSM-IV (Diagnostic and Statistical Manual of Mental Disorders) and DSM-III) have been studied.
The aim of the present study is to test the reliability, validity and acceptance of the newly developed digital version of the Kinder-DIPS, the Kinder-eDIPS, in both a clinical and a non-clinical sample.
Study Type
Observational
Enrollment (Actual)
205
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
North-Rhine Westphalia
-
Bochum, North-Rhine Westphalia, Germany, 44780
- Ruhr-University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
All families with children in the according age group who are willing to complete the structured interview and the questionnaires of the online-survey are allowed to take part in the study.
Description
Inclusion Criteria:
- sufficient knowledge of the German language
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Clinical sample
Participants will be recruited from families in Bochum who receive treatment or wait for the treatment to begin at the Forschungs- und Behandlungszentrum (FBZ; outpatient treatment center).
|
The Kinder-eDIPS is a digital, structured interviews which assesses the most frequent psychological disorders.
It exists in a parent and a child version.
It can be delivered by trained clinicians and takes between 60 and 120 minutes.
|
|
Nonclinical sample
Participants will be recruited from families in Bochum who take part in experiments and studies at the Department of Clinical Child and Adolescent Psychology at the Ruhr-University.
The Department of Clinical Child and Adolescent Psychology maintains a database of families interested in participating in research.
|
The Kinder-eDIPS is a digital, structured interviews which assesses the most frequent psychological disorders.
It exists in a parent and a child version.
It can be delivered by trained clinicians and takes between 60 and 120 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Kinder-eDIPS
Time Frame: within 1 week of the other measures
|
digital, structured interview for children, adolescents and their parents/primary carers
|
within 1 week of the other measures
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Strengths and Difficulties Questionnaire (SDQ)
Time Frame: within 1 week of the other measures
|
Questionnaire assessing emotional symptoms,conduct problems, hyperactivity/inattention, peer relationship problems and prosocial behaviour in 4-17 year olds (child and parent version)
|
within 1 week of the other measures
|
|
Spence Children's Anxiety Scale (SCAS)
Time Frame: within 1 week of the other measures
|
Questionnaire assessing anxiety symptoms in 7-17 year olds (child and parent version)
|
within 1 week of the other measures
|
|
Short Mood and Feelings Questionnaire (SMFQ)
Time Frame: within 1 week of the other measures
|
Questionnaire assessing depressive symptomology in 6-17 year olds (child and parent version)
|
within 1 week of the other measures
|
|
Child and Adolescent Trauma Screening (CATS)
Time Frame: within 1 week of the other measures
|
Questionnaire assessing potentially traumatic events and posttraumatic stress symptoms in 7-17 year olds (child and parent version)
|
within 1 week of the other measures
|
|
Short form of the Eating Disorder Examination-Questionnaire adapted for children (ChEDE-Q8)
Time Frame: within 1 week of the other measures
|
Questionnaire assessing eating disorder psychopathology in 7-18 year olds (only child version)
|
within 1 week of the other measures
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acceptance of the Interview
Time Frame: within 1 week of the other measures
|
Questionnaire assessing children's/adolescent's and parent's perception of the interview
|
within 1 week of the other measures
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Silvia Schneider, Prof., Ruhr-University
- Principal Investigator: Ruth von Brachel, Dr., Ruhr-University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 3, 2021
Primary Completion (Actual)
May 6, 2024
Study Completion (Actual)
May 6, 2024
Study Registration Dates
First Submitted
August 21, 2023
First Submitted That Met QC Criteria
August 21, 2023
First Posted (Actual)
August 25, 2023
Study Record Updates
Last Update Posted (Actual)
June 6, 2025
Last Update Submitted That Met QC Criteria
June 3, 2025
Last Verified
June 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 737
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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