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RECRUITING
NCT06732089

Digital Interventions for Adults with Treatment-Resistant Depression: a Pilot Study

Sponsor: Unity Health Toronto

View on ClinicalTrials.gov

Summary

The goal of this observational study is to learn about remote mental health monitoring technology for adults with treatment-resistant depression. The main question it aims to answer is: are digital mental health monitoring tools (an electronic data capture platform and wearable device (e.g., smartwatch or smart-ring)) feasible to implement alongside clinical treatment for depression? The secondary aim of this study is to inform preliminary clinical parameters for larger, definitive studies. Participants receiving neuropsychiatric treatment (repetitive transcranial magnetic stimulation, intravenous ketamine, or electroconvulsive therapy) as part of their regular medical care for treatment-resistant depression in the Interventional Psychiatry Program will have their clinical assessment data entered into a digital platform and will wear an accessory-based wearable device for the duration of treatment.

Official title: Determining the Feasibility of Digital Interventions for Adults with Treatment-Resistant Depression

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

200

Start Date

2024-12-16

Completion Date

2026-12

Last Updated

2024-12-13

Healthy Volunteers

No

Locations (1)

St. Michael's Hospital, Unity Health Toronto

Toronto, Ontario, Canada