Recruiting

Mood Disorders

Sponsor:

St. Joseph's Healthcare Hamilton

Code:

NCT06408012

Conditions

Mood Disorders

Depressive Disorder

Bipolar and Related Disorders

Eligibility Criteria

Sex: All

Age: 16+

Healthy Volunteers: Accepted

Study Details

Brief summary:

Mood disorders such as depression and bipolar disorder affect over 350 million people around the world. While several effective treatments exist, it is often difficult to match the right treatment to an individual person. Repeated efforts to find the right treatment contribute to poor functioning, low quality of life, and prolongs the time it takes to get well. Most areas of medicine are able to use 'biomarkers' or clinical tests, blood tests, or imaging to help diagnose and treat illness. The search for biomarkers in mood disorders is advancing, but one roadblock to progress is the lack of large, standardized studies of mood disorders that are needed to accurately identify biomarkers. The aim of the ENABLE platform is to provide the Canadian neuroscience community a standardized way of collecting biomarker data from individuals with a range of mood disorders symptoms. In addition, this 'master clinical trial platform' framework will provide a pool of participants who can be recruited into biomarker-based clinical trials.

Conditions

Mood Disorders

Depressive Disorder

Bipolar and Related Disorders

Study ID

NCT06408012

Start date

Oct 17, 2023

Status verified date

Jul, 2026

Completion date

Mar 31, 2029

Anticipated

Primary completion date

Mar 31, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 16+

Healthy Volunteers: Accepted

Inclusion Criteria

Patients:

1. 16 years of age or older.
2. Meet criteria for bipolar or depressive disorders as defined by DSM-5.
3. Fluency in English, sufficient to complete the interviews and self-report questionnaires.

Inclusion Criteria

Healthy Comparison (HC) Participants:

1. 16 years of age or older.
2. No history of psychiatric disorders (according to DSM-5) or significant unstable medical conditions.
3. Fluency in English, sufficient to complete the interviews and self-report questionnaires.

Study Design

Enrollment

2200 participants

Anticipated

Interventions and Outcome Measures

Primary outcome measure

  • Rate of participation in the master trial platform [ Time Frame: 31st March 2026 ]

Central Contacts and Locations

Central contacts

Locations

University of Calgary

Recruiting

Calgary, Alberta, Canada, T2N 4Z6

Contacts

Principal Investigator:

Valerie H Taylor, MD, PhD

University of British Columbia

Recruiting

Vancouver, British Columbia, Canada, V6T 2A1

Contacts

Principal Investigator:

Raymond W Lam, MD

Nova Scotia Health Authority

Recruiting

Halifax, Nova Scotia, Canada, B3H 2E2

Contacts

Principal Investigator:

Rudolf Uher, MD

McMaster University

Recruiting

Hamilton, Ontario, Canada, L8P 3B6

Contacts

Principal Investigator:

Benicio N Frey, MD, PhD

Queen's University

Recruiting

Kingston, Ontario, Canada, K7L4X3

Contacts

Principal Investigator:

Roumen Milev, MD, PhD

University of Ottawa

Recruiting

Ottawa, Ontario, Canada, K1Z 7K4

Contacts

Principal Investigator:

Pierre Blier, MD, PhD

University Health Network

Recruiting

Toronto, Ontario, Canada, M5T 2S8

Contacts

Principal Investigator:

Joshua Rosenblat, MD

Centre for Addiction and Mental Health

Recruiting

Toronto, Ontario, Canada, M6J 1H4

Contacts

Aidan Schottler-Raymond

Aidan.Schottler-Raymond@camh.ca

Principal Investigator:

Lena Quilty, PhD

Ontario Shores Centre for Mental Health Sciences

Recruiting

Whitby, Ontario, Canada, L1N 5S9

Contacts

Principal Investigator:

Daniel Mueller, MD, PhD

More Information

Sponsor

St. Joseph's Healthcare Hamilton

Last update posted

Jul 13, 2026

Last verified

Jul, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by St. Joseph's Healthcare Hamilton on 2026-07-13.