- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00274365
Consultations in Psychiatry Through Videoconference
January 28, 2009 updated by: Sha'ar Menashe Mental Health Center
Consultations in Psychiatry Given to GP's Through Videoconference
Online consulatations through videoconference in the field of psychiatry given to general practitioners will reduce costs of medical treatment and improve service.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
CLINICAL STATE, SATISFACTION AND COST EFFECTIVENESS WILL BE CHECKED DURING 1 YEAR OF ONLINE VIDEO CONFERENCE CONSULTATION TO GENERAL PRACTITIONERS.
BPRS, HAMILTON ANXIETY AND DEPRESSION AND CGI SCALES WILL BE COMPLETED.COSTS OF MEDICATIONS, NUMBER OF VISITS, LAB AND OTHER EXAMINATIONS, HOSPITALIZATIONS, MISSING WORKING DAYS WILL BE EVALUATED.
Study Type
Interventional
Enrollment
250
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
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Hadera, Israel
- Regional clinic of General Health Services
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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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
Referral by general practitioner Age: >18 - Speaking Hebrew or Russion
Exclusion Criteria:
CGI>4 Dementia Drug or alcohol addiction -
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
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Satisfaction
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CGI
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Expenditures on medications
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No. of visits
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Loss of work days
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Expenditure on lab tests
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Hamilton
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Somatisation
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GHQ11
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Q-LES-Q-18
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No. of consultations
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Study Director: Ilan Modai, MD, MHA, Ruth and Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel
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
November 1, 2005
Study Completion (Actual)
February 1, 2007
Study Registration Dates
First Submitted
January 9, 2006
First Submitted That Met QC Criteria
January 9, 2006
First Posted (Estimate)
January 10, 2006
Study Record Updates
Last Update Posted (Estimate)
January 29, 2009
Last Update Submitted That Met QC Criteria
January 28, 2009
Last Verified
April 1, 2007
More Information
Terms related to this study
Other Study ID Numbers
- 4669ctil
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.