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NCT05964322Completed

Cardiac Rehabilitation of Children and Adolescent With Long QT Syndrome

Source: ClinicalTrials.gov · Last updated 31 Jul 2025

Brief summary (registry, in English)

Children and adolescents with inherited cardiac arrhythmia su ch Long QT Syndrome (LQTS) have lower physical and quality of life than their healthy peers. A multi-component cardiac rehabilitation, including an exercise training program and education program, might counteract those effects. The goal of this pilot study is to evaluate the security, feasibility, and benefits of a cardiac rehabilitation program in children with LQTS aged between 6 to 18 years old. The main question\[s\] it aims to answer are: * Is center-based cardiac rehabilitation safe and feasible for children with LQTS? * Does a 12-week cardiac rehabilitation program improve physical fitness and quality of life?

Status (registry)
Completed
Study type
Observational
Enrollment
8 (actual)
First submitted
4 Jul 2023
Start date
2 Feb 2022
Primary completion date
7 Mar 2023
Lead sponsor
University Hospital, Montpellier
NCT number
NCT05964322

What you commit to

  • Study type: Observational
  • Participants enrolled: 8
  • From 2 Feb 2022 to the primary completion date, 7 Mar 2023
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • Children and adolescents, aged 6 to 18 years old, diagnosed with congenital LQTS and had been recently under medical check-up in our last study QUALIMYORYTHM
  • With impaired cardiorespiratory fitness (VO2 peak \<80% of predicted values or VAT \<55% of predicted values) or with normal cardiorespiratory fitness but requiring patient education and information on limits/security in taking part in sports participation.
  • Willingness and ability for parents and children to take part in a 12-week center-based program (e.g., availability during the school period, transportation options)
  • Informed consent of parents or legal guardians, and oral assent of children.

Age in the registry: 6 years to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital of Montpellier - Arnaud de Villeneuve Hospita
Coordinator of this site? Confirm its status
MontpellierFranceUnknown status
Saint-Pierre Institute
Coordinator of this site? Confirm its status
Palavas-les-FlotsFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.