- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00292058
Comparing Telepsychiatry and In-person Outcomes
September 23, 2019 updated by: Lawson Health Research Institute
Comparing Patient Outcomes and Cost of Psychiatric Care Provided Through Videoconferencing With Psychiatric Care Provided In-person.
Psychiatric consultation and short-term follow-up will produce equivalent clinical outcomes and be less costly when provided via videoconferencing (telepsychiatry) than when provided in-person.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
We predict that patients referred by their family physician for a psychiatric consultation and, if needed, short-term follow-up will have equivalent clinical outcomes when seen via telepsychiatry as compared to those patients seen in-person.
We also predicted that telepsychiatry will be cheaper than in-person care.Study Design: a single-centre equivalence trial.We will use a sample size calculation and analytical methods that are specifically tailored for equivalence trials.
Study Type
Interventional
Enrollment
495
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Thunder Bay, Ontario, Canada
- Thunder Bay Regional Health Science Centre
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- patients referred by their family physicians for psychiatric consultation
- scores in the dysfunctional range on the Brief Symptom Inventory
Exclusion Criteria:
- patients incapable of consenting to the research
- patients referred for medico-legal or insurance reports
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
Brief Symptom Inventory
|
Cost of providing the psychiatric services
|
Secondary Outcome Measures
Outcome Measure |
---|
Quality of Life Inventory
|
Client Satisfaction Questionnaire
|
Hospital Utilization
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Richard L O'Reilly, M.B., Lawson Health Research Institute
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2001
Study Completion
August 1, 2004
Study Registration Dates
First Submitted
February 14, 2006
First Submitted That Met QC Criteria
February 14, 2006
First Posted (Estimate)
February 15, 2006
Study Record Updates
Last Update Posted (Actual)
September 25, 2019
Last Update Submitted That Met QC Criteria
September 23, 2019
Last Verified
February 1, 2006
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 07911E
- 7764101
- R2354A01
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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