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

NCT06732089 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2024-12-13

No results posted yet for this study

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.

Conditions

Sponsors & Collaborators

  • University of Toronto

    collaborator OTHER

  • Toronto Metropolitan University

    collaborator OTHER

  • Unity Health Toronto

    lead OTHER

Principal Investigators

  • Dr. Srihar Krishnan, Ph.D., Peng., F.C.A.E. · Toronto Metropolitan University

  • Dr. Wendy Lou, Ph.D. · Dalla Lana School of Public Health, University of Toronto

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-12-16
Primary Completion
2026-10-31
Completion
2026-12-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06732089 on ClinicalTrials.gov