Skip to content

Exercise in Patients With a Biventricular Pacemaker

Effects of an Exercise Program on the Tendance to Severe Arrhythmias in Patients With Severely Impaired Left Ventricular Function and Cardial Re-synchronisation Therapy

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00905944
Enrollment
45
Registered
2009-05-21
Start date
2009-12-31
Completion date
2009-12-31
Last updated
2009-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Left Ventricular Failure

Keywords

Left ventricular failure, chronic heart failure, Pacemaker, Resynchronisation therapy, Exercise, Endurance exercise

Brief summary

The investigators will evaluate the effects of an exercise program (walking on a treadmill) on the physical performance, the cardiorespiratory function, the proclivity to heart arrhythmias and the quality of life of patients with severely impaired left ventricular function and a bi-ventricular resynchronization pacemaker.

Interventions

The patients carry out an exercise program (walking on a treadmill) three times weekly for 12 weeks at a speed corresponding with an intensity of 70% of VO2max.

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Left ventricular failure * Resynchronization therapy with a biventricular pacemaker * Ability to understand written German

Exclusion criteria

* Age over 75 years * Severe cardiac arrhythmia * All conditions which can be aggravated by an exercise program

Design outcomes

Primary

MeasureTime frame
Maximal oxygen uptake (VO2max)At recruitment and after 12 weeks

Secondary

MeasureTime frame
Body mass index (BMI)At recruitment and after 12 weeks
Brain natriuretic peptide (BNP)At recruitment and after 12 weeks
Body compositionAt recruitment and after 12 weeks
MoodAt recruitment and after 12 weeks

Countries

Germany

Contacts

Primary ContactFernando Dimeo, MD
fernando.dimeo@charite.de+493084452098

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026