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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01083823
Other study ID # 364-2007
Secondary ID
Status Completed
Phase N/A
First received March 8, 2010
Last updated April 19, 2012
Start date March 2010
Est. completion date April 2012

Study information

Verified date April 2012
Source Sunnybrook Health Sciences Centre
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

We will modify our existing VMQ/VADIS mood telemetry software to run on a Motorola platform, and enhance it to collect information on both mood symptoms (currently covered by the VMQ/VADIS) as well as daily life stressors (currently outside the VMQ/VADIS' scope). By doing so, we will be able us to examine the role of daily stressors in the lives of teens with and without mood swings, to identify how changes in mood triggered by stressful events are similar to or different from mood changes linked to the bipolar disorder, borderline personality disorder, or other forms of affective instability.


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date April 2012
Est. primary completion date April 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 14 Years to 20 Years
Eligibility Inclusion Criteria:

- Age 14-20yrs,

- Either (i) self-reported healthy with no past / present history of substance use problems OR (ii) self-reported severe mood swings interfering with daily life.

- Fluent in English.

Exclusion Criteria:

- Inability to be trained successfully on the MHT software or to complete questionnaires without assistance.

- Unwillingness to sign / maintain a contract with a cell phone service provider.

- Lack of parental assent / willingness to act as guarantor for cell phone provider contract

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science


Intervention

Other:
Mental health telemetry (MHT)
Use a cell phone equipped with MHT software to complete a self-report mood symptom questionnaire daily at a fixed time of day, as well as additional discretionary questionnaires following any significantly stressful events.

Locations

Country Name City State
Canada Sunnybrook Health Sciences Centre Toronto Ontario

Sponsors (2)

Lead Sponsor Collaborator
Sunnybrook Health Sciences Centre Motorola Canada Limited

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary usability Assessment of participant drop-out and reporting rates After nine months' enrollment No
Secondary Validity Validate that the data reported by telemetry is valid, by comparing cell phone questionnaire responses with results of standardized clinical ratings collected every-three-month via face-to-face meetings Every three months x 9 months No
Secondary Qualitative feedback Collect human factors engineering feedback from our participants for subsequent development work, by questioning participants at the exit interview about their experience with the cell phone and software After nine months' enrollment No
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