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NCT Number: NCT05888688

The Sarcopenia Study

The goal of this cross-sectional study is to investigate the prevalence of sarcopenia in patients with Heart Failure. The main question it aims to answer is:

Whether there is a difference in the prevalence of sarcopenia across the spectrum of HFpEF (Heart failure with preserved ejection fraction) and HFrEF (heart failure with reduced ejection fraction).

This is an observational study. The participant population involves patients with heart failure with preserved ejection fraction and heart failure with reduced ejection fraction. Healthy volunteers will be recruited as controls in addition to adults with asymptomatic Type 2 Diabetes.

Participants will undergo the following:

1. Skeletal muscle mass, quality and body composition assessments using magnetic resonance imaging (MRI) and bioelectrical impedance analysis (BIA) 2. Skeletal muscle strength assessments (Dynamometer, FysioMeter, handgrip strength) 3. Skeletal muscle energetics assessment (31p-Spectroscopy pre/post-exercise recovery)

Researchers will compare Heart failure groups with healthy controls and adults with asymptomatic type 2 Diabetes to see if there are significant differences in the strength, mass and quality of skeletal muscle.

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Key information

About this study

Heart failure is a complex condition which affects the hearts' ability to pump blood around the body properly. Due to this complexity, it often affects multiple systems in the body and can impact the quality of life. A proportion of heart failure patients also have muscle weakness, where one can feel fatigued, and weak, and may have trouble balancing and standing. To characterise muscle weakness, it is important to look at skeletal muscle mass, strength, and function. The study will focus on the prevalence of reduced muscle strength or function, using a variety of assessments within patients with heart failure. The prevalence of muscle weakness will be investigated by running assessments to look into muscle strength, a series of simple exercise tests will be run of the calf and thigh, in addition to a walking test, a balance test and a standing test to assess whole body performance. To look at the quality of skeletal muscle, a magnetic resonance imaging (MRI) and spectroscopy session will allow us to investigate the quality of the thigh muscle and the energetics in the calf. Finally, a muscle biopsy will be performed to understand differences in muscle tissue in people with different types of heart failure.

Overall, this study will provide us with unique information on skeletal muscle strength, composition and energetics within patients with heart failure, by looking at the main factors which characterise muscle weakness.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Heart Failure (HF) Patients: Stage A/B HFpEF

  • Established clinical diagnosis of HFpEF (EF>50%)
  • Clinically stable for ≥ 3 months (no admissions to hospital)
  • Age ≥65
  • Willing to provide written consent for participation in the study.

HF Patients: Stage C/D HFpEF and HFrEF

  • Established clinical diagnosis of HFpEF (EF>50%) OR HFrEF (EF<40%)
  • Clinically stable for ≥ 3 months (no admissions to hospital)
  • Age ≥65
  • Willing to provide written consent for participation in the study. Healthy volunteers
  • Age >18 2. Able to provide written informed consent Asymptomatic T2D
  • Male or female, aged ≥18 and ≤75 years.
  • Diagnosis of stable T2D (determined by i) formal diagnosis in primary care physician case records, ii) a record of diagnostic oral glucose tolerance test OR glycated haemoglobin level ≥6.5%).

Exclusion criteria

Heart failure

  • Absolute contraindication to MRI
  • Inability to walk/undertake the 6-Minute Walk Test (6MWT)
  • Neuromuscular disorders that may impact skeletal muscle assessment, such as motor neurone disease, multiple sclerosis, skeletal muscle myopathies and myositis
  • Regular or intermittent oral corticosteroid use
  • Untreated hyper or hypothyroidism
  • Heart failure-related hospitalisations in the last 3 months

Healthy volunteers

  • Previous or current signs of HF
  • Risk factors for the development of HF, such as hypertension, diabetes Mellitus or coronary artery disease

Asymptomatic Type 2 Diabetes Mellitus (T2D)

  • Angina pectoris or limiting dyspnoea (>NYHA II)
  • Major atherosclerotic disease: Symptomatic CAD, history of MI, previous revascularisation, stroke/transient ischaemic attack or symptomatic peripheral vascular disease.
  • Atrial fibrillation or flutter.
  • Moderate to severe valvular heart disease.
  • History of heart failure or cardiomyopathy.
  • Type 1 diabetes mellitus (T1DM).
  • Low fasting C-peptide levels suggestive of adult-onset T1DM.
  • Stage III-V renal disease (estimated glomerular filtration rate ≤30ml/min/1.73m2).
  • Absolute contraindications to MRI.

Treatment and study plan

Primary outcomes

  1. Volumetric quadriceps skeletal muscle mass (cm^3)

    Time frame: Through study completion, an average of 3 years

    A comparison of volumetric quadriceps skeletal muscle mass (cm3) using MRI between HFpEF and HFrEF patients

Secondary outcomes

  1. HF symptoms and quality of life

    Time frame: Baseline

    Minnesota Living with Heart Failure (MLWHF) questionnaire

  2. Frailty assessment

    Time frame: Baseline

    Edmonton Frail scale

  3. Comparison of Body composition

    Time frame: Baseline

    Bioelectrical impedance analysis (BIA) measure of Appendicular Skeletal muscle (cm^3/height) mass between patient groups

  4. The difference in Muscle fat fraction (percent)

    Time frame: Baseline

    The difference in Muscle fat fraction (%) using MRI (DIXON sequence) of the quadriceps between patient groups

  5. quadriceps Skeletal muscle strength (N)

    Time frame: Baseline

    The difference in quadriceps Skeletal muscle strength (N) between patient groups

  6. Calf plantar flexor strength (N)

    Time frame: Baseline

    The difference in Calf plantar flexor strength (N) (c-station FysioMeter) between patient groups

  7. Handgrip strength (N)

    Time frame: Baseline

    Differences in Handgrip strength (N) (Jamar Dynamometer) between patient groups

  8. A comparison of post-exercise recovery metabolites

    Time frame: Baseline

    A comparison of post-exercise recovery metabolites: Phosphocreatine and inorganic phosphate ratios (PCr/Pi), and Adenosine Triphosphate (ATP) using 31p-Magnetic Resonance Spectroscopy between patient groups

  9. A comparison in distance (metres) walked during 6MWT

    Time frame: Baseline

    A comparison in distance (metres) walked during Six Minute walk test (6MWT) between patient groups

  10. A comparison of daily physical activity

    Time frame: Baseline

    A comparison of daily physical activity behaviours as measured by accelerometry between patient groups

  11. The Short Physical Performance Battery (SPPB) performance

    Time frame: Baseline

    A comparison of lower extremity physical performance following the SPPB test between patient groups

  12. Sarcopenia assessment

    Time frame: Baseline

    SARC-F (Strength, Assistance in walking, Rise from a chair, Climb stairs, and Falls) questionnaire

Other outcomes

  1. quadriceps musculoskeletal Biopsy Analysis

    Time frame: Baseline

    RNA sequencing following biopsy acquisition

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

University of Leicester

Other

Registry information

Official study title

The Imaging Assessment of Sarcopenia Across the Heart Failure Spectrum

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jun 5, 2023
Registry last updated
Dec 19, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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