Identifying Markers of Exercise Training in Heart Failure

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Trial ID: NCT05696652

Purpose

The heart failure syndrome that occurs when the heart is too sick to properly do its job. One of the main symptoms is difficulty with exercise. One way to improve symptoms is to start patients in a 12 week exercise program called cardiac rehabilitation. Cardiac rehabilitation been shown to improve symptoms for heart failure patients. However, the investigators do not know exactly what exercise does to the molecules that make up the human body. If the investigators could answer this question, the investigators might find a whole new way to treat the symptoms of heart failure. Therefore the investigators want to know what molecules might be responsible for the benefits of exercise. The plan for this study is to measure the levels of thousands of proteins in blood samples which come from people with heart failure and see how those levels change after 12 weeks of cardiac rehabilitation, compared to the protein levels in patients whose cardiac rehabilitation is delayed until after the study period. If the investigators know the proteins that change with exercise, the investigators can then look to see if targeting these proteins with medicines can mimic the benefits of exercise. The long term goal of our work is to identify "exercise-in-a-pill" medicines that will help people with heart failure.

Official Title

Identifying Markers of Exercise Training in Heart Failure

Stanford Investigator(s)

Daniel Katz

Instructor, Medicine - Cardiovascular Medicine

Eligibility


Inclusion Criteria:

   - Provision of signed and dated informed consent form

   - Stated willingness to comply with all study procedures and availability for the
   duration of the study

   - Male or female, aged 18-89

   - Patients must carry a diagnosis of heart failure with ejection fraction < 40%

   - Be willing to participate in cardiac rehabilitation, and not already done so in the
   last year

   - Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study
   duration

   - Have a CPET in the last 6 months

   - Must be able to exercise on a treadmill

Exclusion Criteria:

   - Inability to complete CPET or participate in CR (verbal/chart)

   - Syncope during CPET within the last 6 mos, sustained VT on CPET, hemodynamically
   significant arrhythmia during CPET (verbal/chart)

   - BMI >= 38 (verbal/chart)

   - History of a bleeding disorder or clotting abnormality (verbal/chart)

   - Clinical diagnosis of severe Chronic Obstructive Pulmonary Disease (COPD)
   (verbal/chart)

   - History of malignancy not considered in remission (verbal/chart)

   - Cirrhosis (verbal/chart)

   - Thyroid disease (verbal/chart)

      - Thyroid Stimulating Hormone (TSH) value outside of the normal range for the
      laboratory within the last 1 year

         - Individuals with hypothyroidism may be referred to their primary care
         provider (PCP) for evaluation and retested; any medication change must be
         stable for ≥3 months prior to retesting

         - Individuals with hyperthyroidism are excluded, including those with normal
         TSH on pharmacologic treatment

   - Cancer (verbal/chart)

      - History of cancer treatment (other than non-melanoma skin cancer) and not
      "cancer-free" for at least 2 years

      - Anti-hormonal therapy (e.g., for breast or prostate cancer) within the last 6
      months

   - Chronic active or latent infection (verbal/chart)

      - Active or latent infections requiring chronic antibiotic or anti-viral treatment

      - Chronic active infection whether on chronic antimicrobials or not

      - Human Immunodeficiency Virus

      - Active hepatitis B or C undergoing antiviral therapy

      - Individuals successfully treated for hepatitis C and virologically negative for
      at least 6 months are not excluded

   - Tobacco (verbal/chart)

      - Current smokers: any tobacco or e-cigarette/e-nicotine products

      - Former smokers: Stopped smoking <6 months at time of screening

   - Not be pregnant or lactating in the last 12 months, or planning to become pregnant for
   the next 4 months. Not be post-partum during the last 12 months. (verbal/chart)

   - Metabolic bone disease (self-report): History of non-traumatic fracture from a
   standing height or less. Current pharmacologic treatment for low bone mass or
   osteoporosis, other than calcium, vitamin D, or estrogen. (verbal/chart)

   - Diabetes (self-report and screening), which includes: i) treatment with any insulin or
   ii) A1c >=8.0 (screening). (verbal/chart)

   - Chronic renal insufficiency (screening): estimated glomerular filtration rate <30
   mL/min/1.73 m2 from serum creatinine (mg/dL) by the Chronic Kidney Disease
   Epidemiology Collaboration equation. (verbal/chart)

   - Individuals receiving any active treatment for autoimmune disorders (including
   monoclonal antibodies) within the last 6 months. (verbal/chart)

   - Alcohol consumption: i) more than 7 drinks per week for women and more than 14 drinks
   per week for men; ii) history of binge drinking. (verbal/chart)

   - Any individual engaging in night shift work in the last 6 months.

   - Hospitalization for any psychiatric condition within one year (verbal/chart)

   - Any musculoskeletal or ligamentous injury, amputation or congenital neurological
   defect that, in the opinion of the team clinician, would negatively impact or mitigate
   participation in and completion of the protocol. (verbal/chart)

   - Mental incapacity and/or cognitive impairment on the part of the participant that
   would inhibit adequate understanding of or cooperation with the study protocol

   - Other (clinician judgment)

      - Genetic metabolic disorders that could affect metabolomic results (e.g.,
      phenylketonuria)

      - Any other cardiovascular, pulmonary, orthopedic, neurologic, psychiatric,
      metabolic, or other conditions that, in the opinion of the local clinician, would
      preclude participation and successful completion of the protocol

      - Any other illnesses that, in the opinion of the local clinician, would negatively
      impact or mitigate participation in and completion of the protocol

   - Medication exclusions (chart review)

      - Androgenic anabolic steroids, antiestrogens, antiandrogens

      - Growth hormone, insulin like growth factor, growth hormone releasing hormone

      - Insulin of any type used regularly

      - Any drugs used specifically to induce muscle growth/hypertrophy or augment
      exercise induced muscle hypertrophy

      - Psychiatric

         - Chronic use of medium- or long-acting sedatives and hypnotics, including all
         benzodiazepines; short-acting non-benzodiazepine sedative-hypnotics are
         allowed

         - Two or more drugs for depression

         - Mood stabilizers

         - Antiepileptic drugs

         - Stimulants, Attention-Deficit/Hyperactivity Disorder (ADHD) drugs

         - Anti-psychotic drugs

      - Narcotics and narcotic receptor agonists

      - Chronic systemic antimicrobials (antibiotic, antiviral, antifungal, antiparasite,
      etc) for any reason

      - High-potency topical steroids if ≥10% of surface area using rule of 9s

      - Continuous/chronic use of antibiotics or other anti-infectives for treatment or
      prevention

      - Monoclonal antibodies

      - Anti-rejection medications/immune suppressants

      - Any other medications that, in the opinion of local clinicians, would negatively
      impact or mitigate full participation and completion.

Intervention(s):

behavioral: Cardiac rehabilitation

behavioral: Acute exercise

Recruiting

I'm Interested

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305