- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01247519
The Effects of Post-hospitalization Telehealth Care in the Patients Who Admitted Via Emergency Department
November 23, 2010 updated by: National Taiwan University Hospital
The investigators will perform and evaluate a post-hospitalization telecare system for compensating the discontinuity from the hospitalist care system.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
At present, Taiwan's population has become an aging society since recent decade.
Those older than 65 years had achieved 10.4% in 2008.
Meanwhile, the proportion of hosts with underlying comorbid illness or immunocomprised status is increasing worldwide.
In the trend of aging population, telehealth care will be important to extend the care system in post-hospitalization home care.
In the past, thelehealth care has shown a good executive performance in the patients with congestive heart failure and post-operation follow-up.
However, in dealing the patients with acute illness needing hospitalization, the telehealth system has not implemented yet.
In regard to National health insurance (NHI) of Taiwan, hospitalization costs a lot in overall budget.
Reduction of re-hospitalization in those with/without co-morbidity is a important issue for Taiwan NHI.
Therefore, we plan to conduct the telehealth care system in post-hospitalization course in those admitted from emergency department.
We observe the re-hospitalization rate and analyze the risk factors.
In addition, we hypothesize the telehealth care will decrease the rate of re-hospitalization.
Study Type
Interventional
Enrollment (Anticipated)
500
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
-
-
-
Taipei, Taiwan, 100
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Chin-Chung Shu, MD.
- Phone Number: 62477 88623123456
- Email: stree139@yahoo.com.tw
-
-
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:
- Older than 18 years
- Discharged alive from our hospitalist-care ward to home care
- Match diagnosis of general medicine
Exclusion Criteria:
- Younger than 18 years
- Discharged to care facility other than home
- Died in hospital
- Communication deficits
- No telephone at home
- Patient or family refused
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: Prevention
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
|
Post-hospitalization care included telephone call contact for caring after discharge, for opening for question, and for health education.
|
|
No Intervention: observation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
readmission
Time Frame: within 30 days after discharge
|
within 30 days after discharge
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
vist of emergency department
Time Frame: within 30 days after discharge
|
within 30 days after discharge
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Chin-Chung Shu, M.D., National Taiwan University Hospital
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
December 1, 2009
Primary Completion (Actual)
July 1, 2010
Study Completion (Anticipated)
December 1, 2011
Study Registration Dates
First Submitted
October 5, 2010
First Submitted That Met QC Criteria
November 23, 2010
First Posted (Estimate)
November 24, 2010
Study Record Updates
Last Update Posted (Estimate)
November 24, 2010
Last Update Submitted That Met QC Criteria
November 23, 2010
Last Verified
October 1, 2010
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 200912023R
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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