- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05471232
Mental Health Crises in Youth With IDDs
Understanding Mental Health Crises in Youth With Intellectual and Developmental Disabilities
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Aaron Besterman, MD
- Phone Number: 221633 858-576-1700
- Email: abesterman@health.ucsd.edu
Study Contact Backup
- Name: Corrine Blucher, BS
- Phone Number: 221632 858-576-1700
- Email: cblucher@rchsd.org
Study Locations
-
-
California
-
San Diego, California, United States, 92123
- Recruiting
- Rady Children's Hospital San Diego
-
Contact:
- Aaron Besterman, MD, MD
- Phone Number: 858-494-2429
- Email: abesterman@health.ucsd.edu
-
Contact:
- Corrine Blucher, BS
- Phone Number: 221632 8585761700
- Email: cblucher@rchsd.org
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Child/adolescents admitted to the RCHSD ED with an IDD presenting in a MHC that includes, but is not limited to:
- Aggression towards others
- Severe agitation
- Self-injury
- Elopement
OR
Biological parents of child/adolescent enrolled in this study for the purposes of reflex testing. (Family members are eligible for participation in this study if they presumed genetically related to a participant).
Exclusion Criteria:
Child/Adolescents participants who do not meet any of the inclusion criteria, or those who:
- Already received any prior whole genome sequencing or exome sequencing
- Unable to approach the family or patient for enrollment
- Unable to obtain informed consent
- family members are ineligible for participation in this study if they are known to not be genetically related to the child/adolescent participant and/or if they are a member of a protected research population.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Enrollees
These participants will be subject to whole genome sequencing to identify genetic changes and a EHR-Based network model to predict psychiatric outcomes in youth with IDDs.
|
Genomic sequencing results may be used for diagnosis and treatment of participants.
Other Names:
EHR-based network will be created to predict psychiatric outcomes in youth with IDDs
|
|
Historical Control Group
A historical control group from public databases will be used to compare against enrollees.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Extract from Rady EHR demographic, biomedical, socioeconomic, and service use data for 150 youth with IDDs presenting to the ED for MHCs
Time Frame: 4 years
|
Area under the receiver operating characteristic curve for a network model that predicts psychiatric outcomes for youth with intellectual and developmental disabilities.
Area under the receiver operating characteristic curve has a minimum value of 0.5 and a maximum value of 1, where higher scores represent more accurate predictions of psychiatric outcomes.
|
4 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adjusted Relative Risk of Neuropsychiatric Polygenic Scores
Time Frame: 4 years
|
The adjusted relative risk of neuropsychiatric polygenic scores in youth with intellectual and developmental disabilities and mental health crises compared to youth with intellectual and developmental disabilities without mental health crises.
A relative risk of 1 represents equal risk between groups.
A relative risk <1 represents a lower risk in the mental health crisis group and a relative risk of >1 represents a higher risk in the mental health crisis group.
|
4 years
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Diagnostic Rate
Time Frame: 4 years
|
A diagnostic rate of whole genome sequencing will be compared between our primary cohort and two comparator cohorts
|
4 years
|
Collaborators and Investigators
Investigators
- Principal Investigator: Aaron Besterman, MD, MD, Rady Children's Institute for Genomic Medicine
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 801938
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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