NCT02945423

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

15
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Mar 2020

Typical duration for all trials

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 20, 2016

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 26, 2016

Completed
3.3 years until next milestone

Study Start

First participant enrolled

March 1, 2020

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2021

Completed
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2023

Completed
Last Updated

April 10, 2020

Status Verified

April 1, 2020

Enrollment Period

1.6 years

First QC Date

October 20, 2016

Last Update Submit

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

Age10 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

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

Retention: SAMPLES WITH DNA

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

Autistic DisorderCatatonia

Condition Hierarchy (Ancestors)

Autism Spectrum DisorderChild Development Disorders, PervasiveNeurodevelopmental DisordersMental DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsBehavioral SymptomsBehavior

Study Officials

  • Neera Ghaziuddin, M.D.

    University of Michigan

    PRINCIPAL INVESTIGATOR
0

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