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Association Between Lifetime Physical Activity and Exercise and the Development of Wild-type Transthyretin Amyloid Cardiomyopathy

M

Medical University of Graz

Status

Enrolling

Conditions

Amyloid Cardiomyopathy
Wild Type ATTR Amyloidosis

Treatments

Other: Interview

Study type

Observational

Funder types

Other

Identifiers

NCT06261216
01/2023/LPA-wtATTR/NVNS

Details and patient eligibility

About

The aim of this study is to investigate the association between increased lifetime physical activity and the development of wild-type transthyretin amyloid cardiomyopathy.

Full description

Transthyretin amyloidosis is considered to be the most common cause of cardiac amyloidosis, with an increasing diagnosis rate over the last decade. Though once considered to be a rare disease, recent data suggest it is underappreciated as a common cause of cardiac diseases and syndromes such as left ventricular hypertrophy, aortic stenosis, and heart failure with preserved ejection fraction, especially in the elderly. Wild-type transthyretin amyloidosis, which is associated with ageing, is currently considered to be the most frequent form of amyloidosis worldwide, and is dominated by cardiac symptoms. Other than male gender and advanced age, risk factors for the development of wild-type transthyretin amyloid cardiomyopathy (wtATTR-CM) are largely unknown. There is rising empirical observation that patients with wtATTR-CM frequently have a substantial history of athletic activity, which might contribute to the manifestation of the disease.

This study aims to create evidence of a correlation between increased lifetime physical activity and the development of wtATTR-CM. Furthermore, the investigators aim to explore the association between certain sport disciplines and disease development.

Enrollment

189 estimated patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Confirmed diagnosis of wtATTR-CM including sequencing of the TTR gene; or HF; or healthy proband without a diagnosis of heart disease
  2. Initial diagnosis of respective cardiac disease (wtATTR-CM, HF) after the 6th decade of life; or no cardiac disease (healthy control)
  3. Willingness and ability to provide signed informed consent form (ICF)
  4. Age > 60 years

Exclusion criteria

  1. History of severe chronic illness limiting the ability to perform physical activity during the 3rd to 6th decade
  2. A diagnosis of dementia or cognitive impairment
  3. Any other reason resulting in the inability to perform the questionnaire and/or interview
  4. Known disease-causing variant (pathogenic or likely-pathogenic) in the TTR gene

Trial design

189 participants in 3 patient groups

wild-type transthyretin amyloid cardiomyopathy
Treatment:
Other: Interview
heart failure
Treatment:
Other: Interview
healthy controls
Treatment:
Other: Interview

Trial contacts and locations

1

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Central trial contact

Nicolas Verheyen, Res Prof, MD PhD; Nora Schwegel, MD

Data sourced from clinicaltrials.gov

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