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NCT Number: NCT07775196

Aging and Exercise Impacts on Glymphatic Function

This is a prospective, interventional, non-blinded, single center research project that will recruit cognitively unimpaired subjects in the 25-55 year old and 55-75 year old range. This study will use acute aerobic exercise as a natural intervention model to increase cardiac activity which may further drive the glymphatic function. There will be no randomization, and all enrolled subjects will participate in the exercise session.

Hypotheses: revealed by the multi-modal magnetic resonance imaging (MRI) approach, glymphatic dysfunction increases with age and is associated with preclinical Alzheimer's Disease (AD) pathology in cognitively unimpaired individuals. Using acute aerobic exercise as a human model, the enhancement of cerebrospinal fluid-interstitial fluid (CSF-ISF) exchange caused by elevated cardiac activity and paravascular cerebrospinal fluid (pCSF) dynamics can be validated.

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Key information

About this study

The purpose of this research study is to understand how the human brain removes amyloid beta (Aβ) protein which can lead to Alzheimer's disease (AD), using non-invasive magnetic resonance imaging (MRI) techniques. Participants will first go through screening including health survey and blood draw. Depending on their age, enrolled participants will take neuropsychological assessment, sleep and quality-of-life survey, exercise testing, MRI and positron emission tomography (PET) scans. Depending on individual age, the study may include up to three separate visits, a blood draw, an MRI visits and a PET scan visit. The greatest risks of this study include the possibility of injury during the exercise testing, MRI and PET scans, and loss of confidentiality.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • age 25-75 years old
  • cognitively unimpaired (CU)
  • Mini-Mental State Examination (MMSE) score ≥27 at enrollment screening
  • matched gender
  • all racial/ethnic groups

Exclusion criteria

  • pregnant women
  • history of stroke or other major cerebrovascular disease;
  • diagnosis of Alzheimer's disease (AD) or other types of dementia;
  • diagnosis of major neurologic and psychiatric disorders (e.g., Parkingson's disease, major depression);
  • history of prior head trauma, significant autoimmune disorders,
  • sleep apnea;
  • major systemic illness likely to affect the central nervous system, e.g., uncontrolled diabetes, severe cardiovascular disease, cancer, etc.;
  • prior or current alcoholism or drug abuse;
  • resistant hypertension (SBP ≥140 or DBP ≥ 90 mmHg despite 3 antihypertensive drugs at maximal doses);
  • orthostatic hypotension defined as the third standing systolic blood pressure (SBP) < 100mmHg; any contraindications to having a MRI, e.g., claustrophobia, pacemaker or other medical device of metal;
  • any conditions judged by the investigators to be medically inappropriate, risky or likely to cause poor study compliance.

Treatment and study plan

Acute Aerobic exercise

Procedure

During the MRI session, subject will perform aerobic exercise on a MR-compatible ergometer and will be guided to reach certain heart rate level depending on subject's age. Their vital signs will be closely monitored by the research team to ensure safety.

Primary outcomes

  1. Exercise-induced changes in heart rate (HR)

    Time frame: Baseline (pre-exercise), immediately post-exercise

    During exercise, HR will be continuously monitored using photoplethysmography (ppg) by a device attached to a finger of the subjects.

  2. Exercise-induced changes in cardiac output (CO)

    Time frame: Baseline (pre-exercise), immediately post-exercise

    During exercise, CO will be calculated based on HR and real time blood pressure (BP) acquired on the index finger using an MRI-compatible device.

  3. Exercise-induced changes in MRI measurements of pCSF dynamics

    Time frame: Baseline (pre-exercise), immediately post-exercise

    pCSF will be assessed using MRI in the brain.

  4. Exercise-induced changes in MRI measurements of CSF-ISF exchange

    Time frame: Baseline (pre-exercise), immediately post-exercise

    CSF-ISF exchange will be assessed using MRI in the brain.

Study contacts

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

Jiaen Liu, Ph.D.

CONTACT

[email protected]

612/423-8380

Sponsors and collaborators

Lead sponsor

University of Texas Southwestern Medical Center

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Official study title

Impact of Aging and Exercise on Glymphatic Function Using Multi-modal MRI

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Aug 20, 2026
Registry last updated
Aug 20, 2026

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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