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

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.

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

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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