Mental Health Engagement Network (MHEN)

Mood Disorder Clinical Trial

— MHEN  

Official title:

Mental Health Engagement Network (MHEN): Connecting Clients With Their Health Team

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01473550
• Other study ID #: 18451
• Status: Completed
• Phase: N/A
• First received: November 14, 2011
• Last updated: March 4, 2016
• Start date: November 2011
• Est. completion date: June 2014

Study information

• Verified date: March 2016
• Source: Lawson Health Research Institute
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Ethics Review Committee
• Study type: Interventional

Clinical Trial Summary

Patients with mood disorder or psychotic disorder will be given handheld devices with personal health records to educate, monitor and deliver customizable healthcare tools based on their personal needs. The use of technology has great potential to deliver care more effectively and efficiently. No actual information is on the handheld device - it is accessed from a secure site behind hospital firewalls.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 400
• Est. completion date: June 2014
• Est. primary completion date: June 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Must be diagnosed with mood disorder or psychotic disorder for a minimum one year

• Able to make informed consent to participate in the study

• Able to understand and speak English to the degree necessary to participate in interviews/focus groups

Exclusion Criteria:

• Younger than 18 or older than 80

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Health Services Research

Related Conditions & MeSH terms

• Disease
• Mental Disorders
• Mood Disorder
• Mood Disorders
• Psychotic Disorder
• Psychotic Disorders

Intervention

Behavioral:
• Access to TELUS Health Space and Smart Phone
Participants will be given their own TELUS Health Space and Smart Phone in order to have access to their personal health records. Specific procedures using the smart phone will depend on the individual care plan for each participant. Prompts and assessments will vary depending on participant needs.

Locations

Country	Name	City	State
Canada	Canadian Mental Health Association (London-Middlesex Branch)	London	Ontario
Canada	London Health Sciences Centre	London	Ontario
Canada	Regional Mental Health Care	London	Ontario
Canada	Western Ontario Therapeutic Community Hostel	London	Ontario

Sponsors (4)

Lead Sponsor	Collaborator
Lawson Health Research Institute	Canadian Mental Health Association, London Health Sciences Centre, St. Joseph's Health Care London

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Lehman Quality of Life - Brief Version		Every 6 months for total of 18 months	No