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AgingNCT06540287

Molecular Optimization Via Exercise (MOVE)

An observational study of Aging, run by Buck Institute for Research on Aging at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study is to investigate characteristics of muscle, blood, and urine samples from older adults (ages 65-80) who are either sedentary or athletes performing at an elite level for their age. Read more about this study

Who is it for?
Ages 65 to 80 yearsHealthy volunteers can take part
Conditions the study is for
Aging
What is being tested?
Observational
How many people
80 participants
Where
1 siteUnited States
Study dates
19 Sep 2024to May 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 65 to 80 years
  • All sexes
  • Healthy volunteers accepted
  • Older adult

Study population: Male and female Older Endurance Athletes (OEA) at/over the age of 65 - 80 y (exercising at an elite level for their age - assessed by interview and review of training data and competition/results) Male and female Healthy Older Adults (HOA) at/over the age of 65 -80 y who do not regularly exercise (no more than one day per week lasting no more than 60 mins of regular structured exercise)

  1. Willing and able to provide consent to take part in the MOVE-1 Main Study.
  2. Willing and able to attend study visits and comply with all procedures of study data collection visits.
  3. Able to read and speak English well enough to provide informed consent and understand instructions.
  4. Healthy adults between the age of 65 - 80 y.
  5. BMI >19 to < 35 kg/m2
  6. No personal plans (i.e., vacations or medical procedures) during the expected study period (Screening, Test Visit 1, 2 and Sample Collection Visit).
  7. Older Elite Athletes (OEA):
  • Evidence of current physical activity at an elite level for their age, as well as a consistent history of high activity level. This is assessed by interview, review of training data and/or competition results, and by review of the VO2 max data obtained during Testing Visit 1.
  1. Healthy Older Adults (HOA):
  • Sedentary, defined as self-reporting no more than 1 day per week, lasting no more than 60 minutes, of regular (structured) endurance exercise [e.g., brisk walking, jogging, running, cycling, elliptical, or swimming activity that results in feelings of increased heart rate, rapid breathing, and/or sweating] or resistance exercise (resulting in muscular fatigue) in the past year.
  • Persons bicycling as a mode of transportation to and from work >1 day/week etc. are not considered sedentary.
  • Leisure walkers are included unless they meet the heart rate, breathing, and sweating criteria noted above.
  • Does not have a physically active job, no history of physically active job (i.e., postal worker, fire officer
  • No history of consistent high activity level (meeting above criteria) in the last 25 y.

3.2.2. Main Study Exclusion Criteria

  1. Subject requires assistance with any activity of daily living, excluding continence.
  2. Subject lives in an institutional setting (skilled nursing facility or residential care facility for the elderly).
  3. Abnormal bleeding or coagulopathy (self-report): History of a bleeding disorder, wound healing disorder or clotting abnormality.
  4. Female participants must be post-menopause.
  5. Musculoskeletal conditions that would prevent completion of any required exercise testing.
  6. Elevated blood pressure readings (screening test): Resting Systolic Blood Pressure (SBP) ≥150 mmHg or resting Diastolic Blood Pressure (DBP) ≥90 mmHg
  7. Diabetes (self-report and screening tests): Treatment with any hypoglycemic agents (self-report), fasting glucose >125 mg/dL (screening test; may reassess once), use of hypoglycemic drugs for non-diabetic reasons (self-report).
  8. Pulmonary (self-report): Clinical diagnosis of any chronic pulmonary disease that limits exercise capacity.
  9. Cardiovascular (self-report, screening test, and clinician judgement): Congestive heart failure, coronary artery disease, significant valvular disease, congenital heart disease, serious arrhythmia, pulmonary embolism, stroke, or symptomatic peripheral artery disease (self-report, screening test). Specific criteria used to determine whether a volunteer can undergo the screening CPET follow the American Heart Association (AHA) Criteria [6]. Inability to complete the CPET. Reassessment of the CPET may be allowed under some circumstances (e.g., test was not a maximal effort)
  10. Abnormal blood lipid profile (screening test): Fasting triglycerides >500 mg/dL. Low-density lipoprotein cholesterol (LDL-C) >190 mg/dL
  11. Cancer (self-report): History of cancer treatment (other than non-melanoma skin cancer, or chronic lymphocytic leukemia) and not "cancer-free "for at least 2 years. Anti-hormonal therapy (e.g., for breast or prostate cancer) within the last 6 months.
  12. Chronic active or latent infection (self-report): Active or latent infections requiring chronic antibiotic or anti-viral treatment, excluding herpes simplex virus. 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.
  13. Liver enzyme tests (alanine transaminase, aspartate transaminase) (screening test): >2 times the laboratory upper limit of normal. Reassessment during screening may be allowed under some conditions (e.g., recent use of acetaminophen). Individuals may be referred to their PCP for evaluation; any medication change must be stable for ≥3 months prior to retesting.
  14. Chronic renal insufficiency (screening test): Estimated glomerular filtration rate <60 mL/min/1.73 m2 from serum creatinine (mg/dL) by the Chronic Kidney Disease Epidemiology Collaboration equation. Subjects must be able to produce urine. Reassessment may be allowed under some conditions (e.g., questionable hydration status or other acute renal insult)
  15. Hematocrit (screening test): Hematocrit >3 points outside of the local normal laboratory ranges for women and men. Reassessment may be allowed under certain conditions. Individuals may be referred to their PCP for evaluation; any medication change must be stable for ≥3 months prior to retesting.
  16. Blood donation (self-report): Whole blood donation in the last 3 months or plans for blood donation during the entire protocol period. Platelet or plasma donation in the last week or plans for platelet or plasma donation during the entire protocol period.
  17. Autoimmune disorders (self-report): Individuals receiving any active systemic treatment (including immunosuppressants and/or monoclonal antibodies) within the last 6 months.
  18. Alcohol consumption (self-report): Current consumption of more than 7 drinks per week for women More than 14 drinks per week for men. History of binge drinking in the past five years (≥5 drinks for males or ≥4 drinks for females in a 2-hour period more than once per month)
  19. Tobacco (self-report): Current smokers: any tobacco or e-cigarette/e-nicotine products. Former smokers: Stopped smoking <10 years at time of screening for those with a ≥20 pack-year smoking history. Stopped smoking <5 years at time screening for those with a <20 pack-year smoking history.
  20. Recreational drug use (self-report): Self-reported use ≥3 days/week in any form
  21. Shift workers (self-report): Night shift work in the last 6 months. Planning night shift work during the study period.
  22. Cognitive status (screening): Unable to give consent to participate in and safely complete the protocol, as based on the judgement of the investigators.
  23. Psychiatric illness (self-report and screening test): Hospitalization for any psychiatric condition within one year (self-report).
  24. Weight change (self-report): Weight change (intentional or not) over the last 2 months of >5% of body weight. Plan to lose or gain weight during the study
  25. Lidocaine or other local anesthetic allergy (self-report): Known allergy to lidocaine or other local anesthetic
  26. COVID-19 infection: Individuals who tested positive for COVID-19 but were not hospitalized must be symptom free, at least 14 days (without a negative antigen test) or symptom-free at least 7 days with a negative antigen test on the day of the study visit. A PCR test can be used if antigen tests are not available.
  27. Other (clinician judgement): 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Briannaa Stubbs, DPhil contact

4152092000

bstubbs@buckinstitute.org

John C Newman, MD PhD contact

United States1 site, 1 recruiting
  • Buck Institute for Research on Aging

    Novato, California, 94945

    Brianna Stubbs, DPhil, 415-209-2000 ext. 6709, bstubbs@buckinstitute.org

    Recruiting

Other trials in United States

About this study

Official title: An Observational Study of Aging Biomarkers in Older Elite Athletes Compared to Non-exercising Healthy Older Adults.

This study is to investigate characteristics of muscle, blood, and urine samples from older adults (ages 65-80) who are either sedentary or athletes performing at an elite level for their age. This observational study will include bio-specimen collection, as well as physical and cognitive function testing and body composition.

Read the detailed description

The study will enroll a total of 80 subjects-20 of each gender for each cohort. Participation in the study involves 3 visits that must take place within 12 weeks. Optional l follow up visits may be completed at 12- and 24- months after completion of the main study.

The first visit is a screening and enrollment visit. At this visit, informed consent will be obtained and a detailed medical history, screening blood sample collected, and physical assessment will be performed (including, but not limited to vital signs, resting ECG, body composition). Additionally, an exercise history interview will be performed to assess for cohort eligibility. Participants will be familiarized with testing equipment during the screening visit and will perform the Astrand-Rhyming submaximal bicycle test. A short physical function testing battery will be performed, including the short physical performance battery, 6 minute walk test, grip strength, 1 rep max leg press, and leg press fatigue testing.

The second visit will include maximal exercise testing, quality of life assessment, and cognitive function testing. Participants will be allocated into their cohort at this visit.

The third visit will include thigh muscle sample collection via needle biopsy and blood sample collection.

Conditions
Aging
Being tested
Observational
Keywords
Biomarkers, Healthy older adults, Older elite athletes

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ObservationalOther

    No intervention

Study groups in NCT06540287
Study groupRoleWhat they receive
Group 1 cohort: Healthy Older Adults (HOA)This cohort will include healthy older adults, aged 65y or over, who participate in less than 60 minutes of structured exercise each week.
Receives: Other: Observational
Group 2 cohort: Elite Older Athletes (EOA)This cohort will include healthy older adults, aged 65y or over, who are elite athletes for their age (determined by interview and VO2max)
Receives: Other: Observational

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Muscle cellular aging - spatial transcriptomics

    Differences between athletes and sedentary in muscle spatial transcriptomic between OEA and HOA groups

    Measured: Day 2

  2. Muscle cellular aging - single cell transcriptomics

    Differences between athletes and sedentary in muscle single cell transcriptomic between OEA and HOA groups

    Measured: Day 2

Secondary outcomes (14)
  1. Differences between concentration of proteins in the muscle

    Proteomic analysis to measure differences in protein abundance in EOA vs HOA

    Measured: Day 2

  2. Differences between concentration of metabolites in the muscle

    Metabolomic analysis to measure differences in metabolite abundance in EOA vs HOA

    Measured: Day 2

  3. Differences between function of muscle mitochondria

    Analysis of respiratory function of isolated mitochondria

    Measured: Day 2

  4. Blood metabolites

    Metabolic analysis: differences between athletes and sedentary in blood metabolites

    Measured: Day 2

  5. Blood proteins

    Proteomic analysis: differences between athletes and sedentary in blood protein concentration

    Measured: Day 2

  6. Blood cell immune function

    Differences between athletes and sedentary in blood cell immune function

    Measured: Day 2

  7. Blood cell gene expression

    Differences between athletes and sedentary in blood cell gene expression

    Measured: Day 2

  8. Urine metabolites

    Differences between athletes and sedentary in urine metabolites

    Measured: Day 2

  9. Physical function - VO2 max

    Oxygen uptake measured during a ramp test on a bicycle ergometer

    Measured: Day 1

  10. Physical function - grip strength

    Measured in both hands using a dynamometer

    Measured: Day 1

  11. Physical function - 6 minute walk test

    Measure distance covered in 6 minutes on an indoor walk track

    Measured: Day 1

  12. Physical function - short physical performance battery

    SPBB includes balance, gait speed and chair sit tests, consolidated to one score

    Measured: Day 1

  13. Physical function - leg strength

    Maximal leg press weight will be determined on a gym machine via progressive increases in weight

    Measured: Day 1

  14. Physical function - leg press fatigue

    70% of the maximal leg press weight will be used. Subjects will complete as many repetitions as possible of the 70% weight and number of repetitions will be recorded.

    Measured: Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Aug 2024
  2. Study start19 Sep 2024
  3. Primary completionDec 2026 (estimated)
  4. Study completionMay 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06540287
Sponsor's protocol ID
BUCK_2401
Status last verified
Oct 2024
First submitted
26 Jul 2024
Last updated
8 Oct 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Harridge SD, Lazarus NR. Physical Activity, Aging, and Physiological Function. Physiology (Bethesda). 2017 Mar;32(2):152-161. doi: 10.1152/physiol.00029.2016.

    PubMed 28228482
  • Duggal NA, Pollock RD, Lazarus NR, Harridge S, Lord JM. Major features of immunesenescence, including reduced thymic output, are ameliorated by high levels of physical activity in adulthood. Aging Cell. 2018 Apr;17(2):e12750. doi: 10.1111/acel.12750. Epub 2018 Mar 8.

    PubMed 29517845

Questions about this trial

What is this clinical trial studying?

An observational study of Aging, run by Buck Institute for Research on Aging at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 8 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Briannaa Stubbs, DPhil (4152092000, bstubbs@buckinstitute.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Muscle cellular aging - spatial transcriptomics (time frame: Day 2). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06540287, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Oct 2024.

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