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NCT05454254

Effect of Muscle Strengthening Training in Adults with Fontan Circulation

Completed NA Last updated 12 December 2024
What this trial tests

NA trial testing Individualised muscle strengthening exercise training protocol. in Congenital Heart Disease in 20 participants. Completed in 30 November 2023.

Timeline
15 August 2022
Primary endpoint
30 November 2023
30 November 2023

Quick facts

Lead sponsorUmeå University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment20
Start date15 August 2022
Primary completion30 November 2023
Estimated completion30 November 2023
Sites1 location across Sweden

Drugs / interventions tested

Conditions studied

Sponsor

Umeå University

Who can join

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

Sponsor's own description

Aim: to evaluate the effect of muscle strengthening exercise training in adults with Fontan circulation compared to healthy controls. Hypothesis: adults with Fontan circulation have a relatively lower effect of muscle strengthening exercise training compared to healthy controls.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Positive effects of strength training on dynamic muscle function in adults with Fontan circulation: a pilot study.
    Wikner A, Rinnström D, Johansson K, Bergman F, et al · · 2025 · PMID 41424146 · DOI 10.1017/s1047951125110457

Verify or expand the search:

Other recruiting trials for Congenital Heart Disease

Currently open trials in the same condition.

Other Umeå University 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/NCT05454254.

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