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

NCT ID: NCT00489801

Last Updated: 2009-11-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

115 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-01-31

Study Completion Date

2009-07-31

Brief Summary

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

Detailed Description

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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.

Conditions

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Coronary Heart Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Exercise intervention

Exercise intervention and lifestyle counseling at centre or exercise intervention at home

Group Type OTHER

Exercise

Intervention Type OTHER

Exercise intervention and lifestyle counseling at centre or exercise intervention at home

Interventions

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Exercise

Exercise intervention and lifestyle counseling at centre or exercise intervention at home

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Velux Fonden

OTHER

Sponsor Role collaborator

Bispebjerg Hospital

OTHER

Sponsor Role lead

Responsible Party

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Bispebjerg University Hospital

Principal Investigators

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Bodil Oerkild, MD, ph.d fellow

Role: PRINCIPAL_INVESTIGATOR

Locations

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Bispebjeg Hospital

Copenhagen, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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KF 11 2006-4305

Identifier Type: -

Identifier Source: org_study_id

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