Hospital Versus Home Based Exercise in Patients With Chronic Stable Heart Failure

NCT01480921 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2011-11-29

No results posted yet for this study

Summary

The objective of this study is to compare the effect of monitored, home-based exercise versus hospital-based exercise on the quality of life of patients with congestive heart failure. Secondary objectives are to assess the effect of the intervention on exercise capacity and caregiver burden.

The investigators hypothesize that the exercise training in the home-based environment will be superior to hospital based exercise training.

Conditions

  • Congestive Heart Failure

Interventions

BEHAVIORAL

Home-based exercise training

Participants in the home-based group will be advised to exercise, a minimum of 3 times per week, but will be encouraged to exercise a total of 5-7 days per week as per CACR and ACSM guidelines. Prescriptions will include the same elements of those for the hospital group: * 5-10 min warm-up * 30 min aerobic interval training (walking or stationary bicycle) * 10 min cool-down Home-based participants will be asked to record their exercise in an exercise log book and will receive bi-weekly telephone calls from exercise personnel to monitor progress, assess and document adherence, revise the exercise prescription if necessary and provide support and education. Patient safety will be monitored during each call and serious health concerns will be relayed, with the patient's permission, to their primary health provider. Patients in this group will be encouraged to call the exercise specialist or kinesiologist with concerns or questions throughout the study.

BEHAVIORAL

Supervised hospital-based exercise training

Patients in the hospital-based group will participate in supervised, on-site, group exercise sessions 3 times per week, but will be encouraged to exercise a total of 5-7 days per week as per CACR and ACSM guidelines. Trained exercise personnel (kinesiologists and exercise specialists) will supervise these sessions. Exercise sessions will include: * 5-10 min of warm-up * 30 min of aerobic interval training using stationary cycles, treadmills and arm ergometers * 10 min of cool down Exercise will be tracked by the participant in exercise log books.

Sponsors & Collaborators

  • Heart and Stroke Foundation of Ontario

    collaborator OTHER
  • Hamilton Health Sciences Corporation

    collaborator OTHER
  • McMaster University

    lead OTHER

Principal Investigators

  • Heather M Arthur, PhD · Hamilton Health Sciences Corporation

  • Robert S McKelvie, MD, PhD · Hamilton Health Sciences Corporation

  • Jennifer Kodis, MA · Hamilton Health Scienes

  • Kevin Thorpe, MSc · University of Toronto

  • Catherine Demers, MD, MSc · Hamilton Health Sciences Corporation

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-07-31
Primary Completion
2006-06-30
Completion
2007-11-30

Countries

  • Canada

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01480921 on ClinicalTrials.gov