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Clinical Trials/NCT03610087
NCT03610087
Completed
Not Applicable

Technology-Enabled Collaborative Care for Youth (TECC-Y): A Feasibility Study

Centre for Addiction and Mental Health1 site in 1 country70 target enrollmentJuly 25, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Psychosis
Sponsor
Centre for Addiction and Mental Health
Enrollment
70
Locations
1
Primary Endpoint
Change in patient engagement
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The overall objective is to develop scalable interventions to address the physical health needs of patients affected by early psychosis. The objective of this project is to conduct a feasibility study of a high intensity technology-enabled collaborative care model (CCM) compared to lower intensity self-help modules and email support for early identification and treatment of cardio-metabolic risk factors in youth, ages 16-29, affected by early psychosis.

Registry
clinicaltrials.gov
Start Date
July 25, 2018
End Date
June 30, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Peter Selby

Deputy Physician-in-Chief- Education|Clinician Scientist|Chief, Medicine in Psychiatry Division|CAMH|

Centre for Addiction and Mental Health

Eligibility Criteria

Inclusion Criteria

  • Ages 16 - 29 years
  • Clinician diagnosis of early psychosis (diagnosed in last 5 years)
  • Prescribed psychiatric medication, stable for 4 weeks
  • Access to telephone or internet through computer or mobile

Exclusion Criteria

  • Unable to provide consent
  • Unable to understand English

Outcomes

Primary Outcomes

Change in patient engagement

Time Frame: Baseline, 6-weeks, 12-weeks, and 24-weeks.

The primary outcome is patient engagement will be defined as participant activation in the program measured via self-report levels of perceived benefit from the program.

Secondary Outcomes

  • Healthy Behaviour Change(Baseline, 6-weeks, 12-weeks, and 24-weeks.)

Study Sites (1)

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