Actively Recruiting

Phase Not Applicable
Age: 60Years - 90Years
All Genders
NCT06471569

Role of Aging and Individual Variation in Exercise Training Responsiveness

Led by Duke University · Updated on 2025-11-14

26

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

Sponsors

D

Duke University

Lead Sponsor

N

National Institutes of Health (NIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The primary purpose of this study is to assess the effects of aging on markers of physical reserve and exercise-induced adaptations in resilience in older adults who completed a structured exercise program within the last 15 years (Parent trial: STRRIDE-PD; NCT00962962). This feasibility pilot study will enroll up to 26 participants to complete a 6-month aerobic exercise intervention.

CONDITIONS

Official Title

Role of Aging and Individual Variation in Exercise Training Responsiveness

Who Can Participate

Age: 60Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals who completed participation in the STRRIDE-PD trial (NCT00962962)
  • Body Mass Index (BMI) > 18 and < 45 kg/m2
  • Stable dose (61 month) of any cardiometabolic medications
Not Eligible

You will not qualify if you...

  • Poor vein access
  • Current use of tobacco or any nicotine products, including e-cigarettes
  • Insulin-dependent diabetes
  • Active untreated hypothyroidism with thyroid stimulating hormone (TSH) concentrations > 10.0 uIU/mL
  • Systemic inflammatory or connective tissue disease, chronic infectious disease, chronic pulmonary disease or symptomatic cardiovascular disease with positive functional study by ECG or imaging
  • Current, actively treated malignancy other than dermatologic conditions
  • Absolute contraindications to exercise testing: ongoing unstable angina; uncontrolled cardiac arrhythmia with hemodynamic compromise; active endocarditis; symptomatic severe aortic stenosis; decompensated heart failure; acute pulmonary embolism, pulmonary infarction, or deep vein thrombosis; acute myocarditis or pericarditis; acute aortic dissection; physical disability that precludes safe and adequate testing
  • Relative contraindications to exercise testing: known obstructive left main coronary artery stenosis; moderate to severe aortic stenosis with uncertain relation to symptoms; tachyarrhythmias with uncontrolled ventricular rates; acquired advanced or complete heart block; hypertrophic obstructive cardiomyopathy with severe resting gradient; recent stroke or transient ischemic attack; mental impairment with limited ability to cooperate; uncorrected medical conditions, such as hypertension, significant anemia, important electrolyte imbalance, and hyperthyroidism
  • Modified testing contraindications: acute myocardial infarction (MI) within six months; resting hypertension with systolic or diastolic blood pressures >160/90 mmHg
  • Unable to safely participate in an exercise program per study protocol per PI discretion
  • Planned, intentional weight loss during study

AI-Screening

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Trial Site Locations

Total: 1 location

1

Duke Center for Living

Durham, North Carolina, United States, 27705

Actively Recruiting

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Research Team

J

Johanna L Johnson, MS

CONTACT

L

Leanna M Ross, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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