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NCT01724684 Clinical Trial

Feasibility and Effectiveness of Telehealth in Patients With Chronic Obstructive Pulmonary Disease in Taiwan

Chronic Obstructive Pulmonary Disease Clinical Trial

Official title:
Feasibility and Effectiveness of Telehealth in Patients With Chronic Obstructive Pulmonary Disease in Taiwan

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01724684
Other study ID # 201106097RB
Secondary ID
Status Recruiting
Phase N/A
First received January 2, 2012
Last updated November 7, 2012
Start date December 2011

Study information
Verified date November 2012
Source National Taiwan University Hospital
Contact Chun-Ta Huang, MD
Email huangct@ntu.edu.tw
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Interventional

Clinical Trial Summary

Recent studies have demonstrated the promising potential that telehealth has in management of chronic disease. For COPD patients, implementation of telehealth reduced readmissions, emergency room visits, and exacerbations and was cost-effective. Telehealth as a method of delivering healthcare to remote, resource-deprived areas is not lacking in evidence of benefit; however, the situation about its more widespread use for monitoring purposes is much less clear. To date, most of the studies dealing with telehealth in COPD were conducted in countries covering vast territories. Therefore, it needs to be investigated whether telehealth conveys similar advantages for COPD patients in a small island country.

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Admissions for chronic obstructive pulmonary disease

- Age 20 or more

Exclusion Criteria:

- Discharge against medical advice

- Enrolled in other trials

- Not being discharged to home

- Unconsciousness

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research

Related Conditions & MeSH terms

Intervention

Other:
• Telehealth program

• Usual care

Locations
Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)
Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of Participants with Hospital Readmission at 6 months 6 months No
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