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Mental Health Engagement Network (MHEN)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified November 2011 by Lawson Health Research Institute.
Recruitment status was  Not yet recruiting
Sponsor:
Collaborators:
London Health Sciences Centre
Canadian Mental Health Association
St. Joseph's Health Care London
Information provided by (Responsible Party):
Cheryl Forchuk, Lawson Health Research Institute
ClinicalTrials.gov Identifier:
NCT01473550
First received: November 14, 2011
Last updated: NA
Last verified: November 2011
History: No changes posted

November 14, 2011
November 14, 2011
November 2011
December 2013   (final data collection date for primary outcome measure)
Lehman Quality of Life - Brief Version [ Time Frame: Every 6 months for total of 18 months ] [ Designated as safety issue: No ]
Same as current
No Changes Posted
Not Provided
Not Provided
Not Provided
Not Provided
 
Mental Health Engagement Network (MHEN)
Mental Health Engagement Network (MHEN): Connecting Clients With Their Health Team

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.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Health Services Research
  • Mood Disorder
  • Psychotic Disorder
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.
  • Experimental: Early Intervention
    At Phase 1 (first 3 months of project), the 200 participants in Group 1 will be provided with a Personal Health Record (PHR) through TELUS Health Space, as well as they will be introduced to smart phone technology to ready them for deployment of the prompts and reminders. Two months later, they will be provided with a smart phone.
    Intervention: Behavioral: Access to TELUS Health Space and Smart Phone
  • Experimental: Later Intervention
    A delayed implementation plan will be used (but will have no effect on the standard of care for the remaining 200 participants), so the remaining 200 participants in Group 2 will initially act as a control group, but at Phase 2 (six months later - approximately June 2012) the remaining 200 participants will be introduced to the technology in the same order (PHR -> Smart Phone). Group 2 will have the benefit of any enhancements made during Phase 1 of the project.
    Intervention: Behavioral: Access to TELUS Health Space and Smart Phone
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Not yet recruiting
450
December 2013
December 2013   (final data collection date for primary outcome measure)

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
Both
18 Years to 80 Years
Yes
Contact: Meaghan McKillop, MA 519-685-8500 ext 77098 Meaghan.McKillop@LawsonResearch.com
Contact: Amanda Kurtz, BA 519-685-8500 ext 75896 Amanda.Kurtz@lhsc.on.ca
Canada
 
NCT01473550
18451
No
Cheryl Forchuk, Lawson Health Research Institute
Lawson Health Research Institute
  • London Health Sciences Centre
  • Canadian Mental Health Association
  • St. Joseph's Health Care London
Principal Investigator: Cheryl Forchuk, PhD Lawson Health Research Institute; University of Western Ontario
Lawson Health Research Institute
November 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP