Exercise & Brain Energetics in PD

NCT ID: NCT04426786

Last Updated: 2024-11-06

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-01-26
• Study Completion Date: 2025-12-30

Brief Summary

There is increasing evidence that the usage and delivery of energy to the brain, known as brain energetics, is altered in people with Parkinson's disease (PD). This project will explore whether exercise has a positive impact on brain energetics using functional Magnetic Resonance Imaging (fMRI) and Positron Emission Tomography (PET) brain scanning in PD subjects.

PD subjects will be scanned before and after a supervised exercise program to investigate the effect of exercise on brain energetics. In a separate study, the investigators will also scan healthy volunteers to compare brain energetics in the healthy brain with the brain energetics data in PD subjects acquired in this study.

Detailed Description

Previous work has investigated the link between decreased brain energetics (through mitochondrial dysfunction), though an investigation in-vivo has never been feasible due to technology constraints. Furthermore, recent work has suggested exercise may help reduce the effect of mitochondrial dysfunction. There is thus compelling evidence to investigate brain energetics/mitochondrial function in-vivo, in health, at different stages of disease and the relationship to exercise. While such measurements are intrinsically difficult, a useful measure is expected to be derived from the ratio between the cerebral metabolic rate of oxygen (CMRO2) and the cerebral metabolic rate of glucose (CMRGlu), if they are measured simultaneously. The simultaneous aspect of the two measurements is extremely important as diurnal variations in CMRO2 can be as high as 20%, while those in CMRGlu as high as 38%. Fortunately, given recent advances in measurement technique and instrumentation development, such studies are now becoming possible: CMRO2 can be obtained using very advanced functional magnetic resonance imaging (fMRI) techniques with respiratory manipulations, while CMRGlu can be estimated by positron emission tomography (PET) using the tracer 18F-fluorodeoxyglucose (FDG-PET). A lower-than-normal ratio between CMRO2 and CMRGlu coupled with a decrease in CMRGlu in any brain area is taken to be indicative of locally impaired brain energetics, related to altered mitochondrial function.

The investigators hypothesize that (i) brain energetics, measured as the ratio CMRO2/CMRGlu is altered early in Parkinson's disease (PD) compared to age-matched healthy controls (HC) and continues to be altered as disease progresses; and (ii) exercise will positively affect alterations in brain energetics in PD subjects.

The investigators will recruit up to 30 PD subjects who are not habitual exercisers and up to 10 PD subjects who are habitual exercises. The 30 non-exercisers will undergo a supervised six month exercise intervention in groups, with PET/MRI scans before and after. The 10 exercisers will only be scanned once (for observational comparisons with the non-exercisers at baseline) and will not undergo the exercise intervention. In a separate study, the investigators will recruit up to 30 HCs to compare to compare their brain energetics metrics with those of the PD subjects at baseline to test hypothesis (i). Of the 30 non-exercisers, half will be assigned to start the exercise intervention immediately after their baseline scan, and the other half will have a six month delayed start to the intervention. During the delay, subjects will perform passive exercise in groups, to control for social interaction and possible placebo effects. Longitudinal comparisons of the non-exercisers before and after the intervention will test hypothesis (ii).

The objectives of this study are twofold: to (i) investigate a disease-initiating mechanism (abnormal mitochondrial function and impaired cellular bioenergetics), which could constitute a novel therapeutic target; and to (ii) study the effects of the intervention: while this will be a pilot study, involving limited exercise regimens, any knowledge gained about the impact of exercise on brain energetics will have a tremendous impact on the design of neuroprotective therapies and personalized treatment.

Conditions

Parkinson Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: DOUBLE

Study Groups

Immediate intervention start: active exercise

Immediately starts the six month intervention of active exercise following the baseline scan.

Group Type: ACTIVE_COMPARATOR

Active exercise

Intervention Type: OTHER

Thrice-weekly supervised intense aerobic exercise classes on cycle ergometers, in groups, for six months. Percentage of VO2 max will be used to regulate exercise intensity, based on an initial aerobic exercise test.

Delayed intervention start: passive exercise

Starts the six month intervention of active exercise six months after the baseline scan. During the six month delay, participants in this arm undergo passive exercise.

Group Type: PLACEBO_COMPARATOR

Active exercise

Intervention Type: OTHER

Thrice-weekly supervised intense aerobic exercise classes on cycle ergometers, in groups, for six months. Percentage of VO2 max will be used to regulate exercise intensity, based on an initial aerobic exercise test.

Passive exercise

Intervention Type: OTHER

Thrice-weekly supervised passive exercise classes consisting of stretching and/or yoga, in groups, for six months.

Interventions

Active exercise

Thrice-weekly supervised intense aerobic exercise classes on cycle ergometers, in groups, for six months. Percentage of VO2 max will be used to regulate exercise intensity, based on an initial aerobic exercise test.

Intervention Type: OTHER

Passive exercise

Thrice-weekly supervised passive exercise classes consisting of stretching and/or yoga, in groups, for six months.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Idiopathic PD according to UK Brain Bank criteria (modified to permit inclusion of subjects with a family history)

2. Mild to moderate Parkinsonism (Hoehn & Yahr stages I-III)

3. Currently exercise less than 120 minutes per week (PD non-exercisers)

Exclusion Criteria

1. atypical Parkinson syndrome (progressive supranuclear palsy, multiple system atrophy, drug-induced etc.);

2. significant osteoporosis or arthritis;

3. history of cancer within 5 years of study participation;

4. high dose of radiation from other procedures within the year;

5. not able to tolerate being off PD medication for up to 24 hours;

6. a female subject who is breast-feeding or pregnant;

7. current or past substance use problems;

8. serious head injury with loss of consciousness for ≥ 5 minutes;

9. people with other chronic diseases such as diabetes, kidney problems, high blood pressure, other known neurological disorders, or heart diseases;

10. people who report having a significant respiratory disorder (e.g. asthma, chronic obstructive pulmonary disease (COPD)) or using home oxygen will be excluded to avoid discomfort or breathing difficulties from respiratory manipulations.

11. current or past neurological disorder (e.g. strokes, seizures, neurodegenerative disease other than Parkinson's disease);

12. current or past psychiatric disorders (e.g. depression, anxiety disorders);

13. severe claustrophobia (a fear of closed in spaces);

14. weight of more than 158kg (347 lbs);

15. inability to lay still for up to 90 minutes;

16. are not medically cleared to exercise;

17. certain medications or conditions may impact participant's ability to participate and these will be discussed on a case by case basis with the participant and the study team.

1. Machinist or metalworkers;

2. cardiac pacemakers, wires, or defibrillator;

3. past injury where a piece of metal lodged in your eye or orbit;

4. ferromagnetic aneurysm clip;

5. artificial heart valve;

6. electrical stimulator for nerves or bones;

7. ear or eye implant;

8. implanted drug infusion pump;

9. coil, catheter, or filter in any blood vessel;

10. orthopedic hardware (artificial joint, plate, screws);

11. other metallic prostheses;

12. shrapnel, bullets, or other metal fragments;

13. dentures, braces, or retainer;

14. surgery (brain or otherwise), tattoos, or injection into a joint in the last 6 weeks;

15. pierced body parts (other than earrings) or tattooed eyeliner;

16. non-MRI safe intrauterine device (IUD).

1. significant cognitive impairment or depression;

2. significant or unstable cardiovascular or respiratory disease - all subjects will undergo a screening aerobic exercise test;

3. failure to comply with the exercise intervention program by not completing at least 60 of the 72 exercise classes.

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Natural Sciences and Engineering Research Council, Canada

OTHER

Sponsor Role: collaborator

Pacific Parkinson's Research Centre

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Vesna Sossi

Role: PRINCIPAL_INVESTIGATOR

University of British Columbia

Locations

Pacific Parkinson's Research Centre

Vancouver, British Columbia, Canada

Site Status: RECRUITING

Countries

Canada

Central Contacts

Jessamyn McKenzie

Role: CONTACT

jess.mckenzie@ubc.ca

604 822 7764

Facility Contacts

Jess McKenzie

Role: primary

604-822-7764

Other Identifiers

H19-01839

Identifier Type: -

Identifier Source: org_study_id