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NCT00489801 Clinical Trial

Trial Comparing Home-based Cardiac Rehabilitation With Comprehensive Centre-based Cardiac Rehabilitation in Patients Older Than 65 Years With Coronary Heart Disease. The HOMEBASE Trial

Coronary Heart Disease Clinical Trial

— HOME-BASE  

Official title:
RCT Comparing Home-based Cardiac Rehabilitation With Comprehensive Centre-based Cardiac Rehabilitation and Usual Care in Patients Older Than 65 Years With Coronary Heart Disease. The HOMEBASE Trial.

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00489801
Other study ID # KF 11 2006-4305
Secondary ID
Status Active, not recruiting
Phase N/A
First received June 20, 2007
Last updated November 9, 2009
Start date January 2007
Est. completion date July 2009

Study information
Verified date November 2009
Source Bispebjerg Hospital
Contact n/a
Is FDA regulated No
Health authority Denmark: The Danish National Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

Hypothesis: Home-based cardiac rehabilitation is as effective as comprehensive centre-based cardiac rehabilitation in patients older than 65 years.

Description:

Participation in cardiac rehabilitation is known to reduce mortality and morbidity and increase health related quality of life. However, participation rate are low among elderly cardiac patients with coronary heart disease. Home-based cardiac rehabilitation could be an attractive alternative to the centre-based programmes but studies investigating the effect of these programmes are limited and even less is known about the effect among the elderly.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 115
Est. completion date July 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

1. Event of coronary heart disease (new myocardial infarction, CABG or PCI)

Exclusion Criteria:

1. Care home patients.

2. Serious disability incompatible with rehabilitation.

3. Social circumstances incompatible with participation.

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Other:
• Exercise
Exercise intervention and lifestyle counseling at centre or exercise intervention at home

Locations
Country Name City State
Denmark Bispebjeg Hospital Copenhagen

Sponsors (2)
Lead Sponsor Collaborator
Bispebjerg Hospital Velux Fonden

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary Exercise capacity At baseline and after 3,6 and 12 months No
Secondary Blood pressure, cholesterol, body composition, HRQL At baseline and after 3, 6 and 12 months No
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