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The BC Psychosis Program Biobank and Database for Genetic Polymorphisms and Their Associations With Psychosis Disorder

BC Psychosis Program Biobank and Database for Investigating Genetic Polymorphisms of Brain-derived Neurotrophic Factor and Catechol-o-methyl Transferase and Their Associations With Psychosis Disorder

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02322918
Acronym
BCPP BIODA
Enrollment
200
Registered
2014-12-23
Start date
2014-07-31
Completion date
2018-07-31
Last updated
2016-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psychosis, Schizophrenia

Brief summary

The purpose of this study is to determine if candidate polymorphisms in brain-derived neurotrophic factor (BDNF) and catechol-o-methyl transferase (COMT) are predictive of psychosis disorder severity, symptomology, and resolution in patients at BCPP. A secondary objective will be to form a biorepository of blood and saliva samples from patients at BCPP so that further genetic, proteonomic and pharmacogenomic studies may be done to gain insight into the genetic basis of differences in psychosis disorder presentation and manifestation, and differences in response to antipsychotic drug treatment.

Detailed description

This is a population-based, genetic-association, candidate polymorphism study. It will involve a prospective and a retrospective component. A blood draw or saliva sample will be performed during the participant's admission to BCPP, which may occur at any point during the participant's length of stay. When a participant has been deemed 'Ready for Discharge' by his/her attending psychiatrist at BCPP, a full phenotype will be obtained via retrospective chart review. Genetic analyses and determination of protein levels will be performed after chart review. Following fulfillment of the primary study objective, the remaining blood and saliva samples will be stored in the biobank over the long-term.

Interventions

Participant will receive one blood draw whereby two samples will be extracted. If the participant wishes to participate in the study but is fearful of needles, they may be given the option to provide a saliva sample. A retrospective medical chart review will be performed after participant is discharged from BCPP in order to obtain a full phenotype. Genotyping of BDNF and COMT will be performed. Protein levels of BDNF will be determined. The remaining blood or saliva samples will be stored over the long-term in a biorepository at the BC Mental Health and Addictions Research Institute. A retrospective medical chart review will be completed after the participant is discharged.

Sponsors

Vancouver Coastal Health
CollaboratorOTHER_GOV
University of British Columbia
Lead SponsorOTHER

Study design

Observational model
COHORT

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Admission to BCPP. * Has provided written informed consent.

Exclusion criteria

* None.

Design outcomes

Primary

MeasureTime frameDescription
Creation of biorepository of blood samples for future genetic, proteonomic and pharmacogenomic studies.One visit during participant's stay at BCPP, an expected average of 6 monthsA biobank of stored samples will be used to determine the genetic variability in psychosis disorder.

Secondary

MeasureTime frameDescription
Identification of single-nucleotide polymorphisms (SNPs) in the BDNF and COMT genesOne visit during participant's stay at BCPP, an expected average of 6 monthsWe will determine if specific genetic variants in BDNF and COMT genes are associated with psychosis disorder severity, symptomology and resolution.
Medical Chart ReviewOne visit during participant's stay at BCPP, an expected average of 6 monthsA medical chart review will be done on hard-copy medical charts at BCPP.

Countries

Canada

Contacts

Primary ContactDelrae Fawcett, M.Sc.
delrae.fawcett@ubc.ca604-875-2000
Backup ContactHeidi Boyda, Ph.D.
heidi.boyda@ubc.ca604-875-2000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026