Evaluation Study: Obsessive-compulsive Disorders in Childhood and Young Adulthood
NCT ID: NCT04723485
Last Updated: 2025-05-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
625 participants
OBSERVATIONAL
2020-05-01
2026-03-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Short and Intensive Treatment of Children and Adolescents With Obsessive-Compulsive Disorder
NCT04730011
Characterization of Childhood-Onset Obsessive-Compulsive Disorder
NCT00044239
Cognitive Behavioral Group Treatment for Obsessive-compulsive Disorder in Youth
NCT04891367
A Controlled Trial of Daily Cognitive-Behavioral Therapy for Pediatric Obsessive-Compulsive Disorder
NCT00369642
Internet-delivered CBT for Adolescents With Obsessive-Compulsive Disorder - a Pilot Study
NCT01809990
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Good German language speaking skills
* IQ \> 75
* All study participants or their legal representative have given written permission for their experiences to be documented in the study.
Exclusion Criteria
* Missing data
* Data sets without confirmed diagnosis
* Purely consultaive patient interview (no therapy intervention prescribed)
4 Years
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Susanne Walitza
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Susanne Walitza
Head of the Department of Child and Adolescent Psychiatry
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Susanne Walitza, Prof. Dr. med. Dipl.-Psych.
Role: PRINCIPAL_INVESTIGATOR
Sponsor-Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Psychiatric University Clinics, Department of Child and Adolescent Psychiatry
Zurich, Canton of Zurich, Switzerland
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
KJPP 2019-00230
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.