Study Stopped
funding issues
Improving the Understanding of Catatonia in Autism
A-CAT
1 other identifier
observational
N/A
0 countries
N/A
Brief Summary
Catatonia is a neuropsychiatric syndrome which is frequently missed or misdiagnosed among psychiatric patients. The current project is a systematic examination of catatonia which will characterize the phenotype and identify biological correlates that play a central role in the pathophysiology and effective pharmacological treatment of this condition.
Trial Health
Trial Health Score
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Started Mar 2020
Typical duration for all trials
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 20, 2016
CompletedFirst Posted
Study publicly available on registry
October 26, 2016
CompletedStudy Start
First participant enrolled
March 1, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2023
CompletedApril 10, 2020
April 1, 2020
1.6 years
October 20, 2016
April 8, 2020
Conditions
Outcome Measures
Primary Outcomes (1)
Psychiatric, cognitive and biological identification of catatonia in psychiatric illness
Psychiatric, medical, neuropsychological and biological testing will be completed in approximately 30 subjects and analyzed and reviewed by PI and Co-PIs to determine parameters of catatonia diagnosis in psychiatric patients.
Three months
Eligibility Criteria
Participants will be determined through University of Michigan medical record screening. Participants will be both male and female, between the ages of 10-30 years old (inclusive) and will have a previous diagnosis of catatonia, not secondary to a medical condition.
You may qualify if:
- Age range = 10 to 30 years.
- Already diagnosed with Catatonia during 2005 to 2015.
- Inclusive of current symptoms or have had symptoms in past (symptom
You may not qualify if:
- \. Onset of catatonia is clearly secondary to general medical condition
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Biospecimen
DNA: one 8ml vial of blood will be drawn and stored for future DNA analysis. DNA will be stored as part of the Heinz C. Prechter Genetics Repository.Once the DNA is extracted and genotyped, researchers will sequence the genetic information for specific variants. All samples and data will be de-identified.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Neera Ghaziuddin, M.D.
University of Michigan
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
October 20, 2016
First Posted
October 26, 2016
Study Start
March 1, 2020
Primary Completion
October 1, 2021
Study Completion
October 1, 2023
Last Updated
April 10, 2020
Record last verified: 2020-04