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The goal of this clinical trial is to assess the efficacy of CBT-NC intervention to determine its impact on mental health and suicidality in children ages 6-17. The main aims are: Aim 1: Examine CBT-...
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Lead Sponsor
University of Oklahoma
Collaborators
NCT05988489 · Suicidal Ideation
NCT04794595 · Sepsis, Children, Only
NCT06441864 · Nightmare, Nightmare Disorder With Associated Other Sleep Disorder, and more
NCT07025720 · Major Depressive Disorder (MDD), Suicidal Ideation
NCT06804525 · Major Depressive Episode (MDE), Major Depressive Disorder (MDD), and more
University of Tulsa
Tulsa, Oklahoma
University of Oklahoma School of Community Medicine
Tulsa, Oklahoma
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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