Condition: Nightmare · Suicidal Ideation · Children, Only · Sponsor: University of Oklahoma
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-NC efficacy for improving nightmare distress and frequency in youth with chronic nightmares by comparing the treatment and waitlist group. Aim 2: Examine whether improvements in nightmares relate to fewer mental health problems for youth by determining by comparing the treatment and waitlist group.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
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| University of Tulsa | Tulsa, Oklahoma, United States | — |
| University of Oklahoma School of Community Medicine | Tulsa, Oklahoma, United States | — |
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