Last reviewed · How we verify

NCT05696990

3/7 Resistance Training Method in Cardiac Rehabilitation

Completed NA Last updated 15 February 2024
What this trial tests

NA trial testing 3/7 Resistance Training Method in Heart Failure in 112 participants. Completed in 30 August 2023.

Timeline
1 January 2019
Primary endpoint
1 March 2023
30 August 2023

Quick facts

Lead sponsorUniversité Libre de Bruxelles
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment112
Start date1 January 2019
Primary completion1 March 2023
Estimated completion30 August 2023
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Université Libre de Bruxelles — full company profile →

Who can join

18 and older, any sex, with Heart Failure or Coronary Artery Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Aim of the clinical monocentric study is to assess the resistance training exercise intervention in patients with Heart Failure with reduced Ejection Fraction (HFrEF) and coronary artery disease that will best improve peak oxygen uptake (Peak Vo2) and leg strength (assessed Isokinetic). The investigators hypothesize that resistance training exercise with induced a high stress metabolic is more important exercise with induced than a lower stress metabolic.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Heart Failure

Currently open trials in the same condition.

Other Université Libre de Bruxelles trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05696990.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing