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NOT YET RECRUITING
NCT07656870

Exploring the Genetics of Schizophrenia in Manitoba

Sponsor: University of Manitoba

View on ClinicalTrials.gov

Summary

Schizophrenia is a serious mental illness that affects about 1 in 100 Canadians, shortens life expectancy, and places a large burden on individuals, families, and the healthcare system. Genetics are known to play a major role, but current research explains only part of the inherited risk because most studies have looked at only a small portion of the genome and have mainly focused on people outside Canada. This project will create the first large-scale Manitoba-based schizophrenia whole-genome sequencing database by studying 1,500 Manitobans with and without schizophrenia using both short-read and advanced long-read genome sequencing technologies. Researchers will combine genetic data with lifelong provincial health records to better understand rare genetic variants linked to schizophrenia and how genetic differences influence medication response, side effects, hospitalizations, and treatment outcomes. The study aims to fill important gaps in schizophrenia research in Canada, improve understanding of the disorder's biology, and support the development of more personalized and effective treatments for people living with schizophrenia.

Official title: Uncovering Schizophrenia Genetics Through Whole Genome Sequencing Across Manitoba

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

1500

Start Date

2026-08

Completion Date

2031-04

Last Updated

2026-06-18

Healthy Volunteers

Yes

Locations (1)

University of Manitoba

Winnipeg, Manitoba, Canada