Psychiatric Consultation Through Videoconference in a Primary Care Setting
Recruitment status was Not yet recruiting
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Purpose
In our study we will aim to examine the issues of cost analysis, quality of life, clinical efficacy and satisfaction of psychiatric consultations through videoconference in a primary care setting in comparison with in-person psychiatric treatment and primary care only. The main hypotheses of the study are: Satisfaction of the patients will increase, the use of telepsychiatry will reduce the costs for the primary and mental health care centers as well as for the patients, the treatment will be as effective as in-person treatment, the number of patients referred to mental health treatment will be higher than that of the previous year, quality of life will improve and that there will be a stigma reduction of mental illness.
| Condition | Intervention |
|---|---|
|
Remote Consultation Community Psychiatry |
Device: Videoconference equipment FALCON/IP |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Telepsychiatry: Cost Analysis, Quality of Life, Satisfaction and Effectiveness of Psychiatric Consultation Through Videoconference in a Primary Care Setting |
- Brief Psychiatric Rating Scale (BPRS) at 0 months, 6 months and 12 months.
- Clinical Global Impression Scale (CGI) at 0 months, 6 months and 12 months.
- Hamilton Anxiety Rating Scale (HAM-A) at 0 months, 6 months and 12 months.
- Hamilton Depression Rating Scale (HAM-D) at 0 months, 6 months and 12 months.
- Global satisfaction questionnaire at 0 months, 6 months and 12 months.
- General Health Questionnaire 11 (GHQ11) at 0 months, 6 months and 12 months.
- Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q-18) at 0 months, 6 months and 12 months.
- Costs: Travel expenses, extra consultations, hospitalizations, Medication, loss of work days, medical visitations, ancillary tests such as ECG, lab tests and others at 0 months, 6 months and 12 months.
| Estimated Enrollment: | 160 |
| Study Start Date: | May 2006 |
| Estimated Study Completion Date: | November 2007 |
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Patients referred by the primary care physician.
- Age 18 and over.
- Speak Hebrew.
Exclusion Criteria:
- Patients that suffer from severe dementia.
- Patients suffering from addiction to drugs or alcohol.
- Patients who are deaf, dumb or blind.
- Patients who have a legal guardian.
Contacts and Locations| Contact: Mahmud Jabarin, MD | +972-4-6278110 | jabarin@shaar-menashe.org.il |
| Contact: Ehud Susser, MD | +972-4-6278946 | udiwudi@yahoo.com |
| Israel | |
| Sha'ar Menashe Mental Health Center Ambulatory Clinic | Recruiting |
| Hadera, Israel, 38814 | |
| Contact: Mahmud Jabarin, MD +972-4-6278110 jabarin@shaar-menashe.org.il | |
| Contact: Ehud Susser, MD +972-4-6278946 udiwudi@yahoo.com | |
| Principal Investigator: Mahmud Jabarin, MD | |
| Principal Investigator: | Mahmud Jabarin, MD | Sha'ar Menashe Mental Health Center, Israel |
| Study Chair: | Ilan Modai, MD, MHA | Sha'ar Menashe Mental Health Center, Israel |
| Study Chair: | Ehud Susser, MD | Sha'ar Menashe Mental Health Center, Israel |
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00298961 History of Changes |
| Other Study ID Numbers: | TelepsychiatryCTIL |
| Study First Received: | March 2, 2006 |
| Last Updated: | May 20, 2008 |
| Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
ClinicalTrials.gov processed this record on June 17, 2013