Fact CheckerSign in

NCT06833944Recruiting

High Intensity Interval Training in the Treatment of Familial Hypercholesterolemia (UPPA-FH)

Unraveling the Potential of Physical Activity in the Treatment of Familial Hypercholesterolemia: Impact of Exercise on Cardiorespiratory Fitness, Atherosclerosis Progression, and Underlying Mechanisms

Source: ClinicalTrials.gov · Last updated 22 Sept 2026

Brief summary (registry, in English)

This study has one main objective: a) To assess the impact of two different supervised exercise interventions on cardiorespiratory fitness and markers of subclinical atherosclerosis in patients with Familiar Hipercolesterolemia (FH), and to unravel the underlying mechanisms behind these effects. The starting hypothesis of the UPPA-FH project anticipates that both exercise interventions will produce a large increase in cardiorespiratory fitness and will improve significant markers of atherosclerosis in patients with FH, with high-intensity interval training program (HIIT) being more efficient than the moderate-intensity continuous training (MICT) modality. The main effects will be mediated by a significant change in the metabolomic signature of the participants. In addition, higher physical activity will be associated with more favorable markers of atherosclerosis progression, as shown through blood and image technique

Status (registry)
Recruiting
Study type
Interventional
Enrollment
75 (estimated)
First submitted
27 Jan 2025
Start date
20 Feb 2025
Primary completion date
28 Feb 2027
Lead sponsor
Fundación Pública Andaluza para la Investigación Biomédica Andalucía Oriental
NCT number
NCT06833944

What you commit to

  • Study type: Interventional
  • Planned participants: 75
  • From 20 Feb 2025 to the primary completion date, 28 Feb 2027
  • 1 site 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.

Other illness

  • History of clinical CVD (ischemic heart disease, stroke, and/or peripheral arterial disease).

Other

  • Inability to read, understand and sign the informed consent.
  • Contraindications to exercise.

Who the study is looking for

  • Individuals with a diagnosis of genetic FH.
  • \> 18 years old.
  • Minimum follow-up of 1 year in the Vascular Risk Clinic of the Virgen de las Nieves University Hospital (HUVN).
  • Clinical and treatment stability.
  • Non-pathological angio-TAC of coronary arteries in the 2 years prior to the study (for participants \>45 years old).

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Virgen de las Nieves University Hospital
Coordinator of this site? Confirm its status
GranadaSpainRecruiting

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