Long Term Aerobic Exercise to Slow Progression in Parkinson's Disease
Overview
- Phase
- Not Applicable
- Intervention
- Aerobic walking
- Conditions
- Parkinson's Disease
- Sponsor
- VA Office of Research and Development
- Enrollment
- 57
- Locations
- 2
- Primary Endpoint
- Change in MDS-UPDRS Part III Motor (OFF) Score
- Status
- Completed
- Last Updated
- last month
Overview
Brief Summary
Parkinson's disease (PD) is an incurable brain illness that afflicts more than one million Americans, including many aging Veterans. PD places an unbearable burden on the individual due to progressive impairment of movement and mental function. As a result, patients lose critical abilities such as driving and can become isolated. Although drugs and surgery help movement problems, their benefits are temporary and may cause side effects. Drugs provide limited and temporary benefit for cognition and do not prevent dementia. Animal and preliminary human studies on aerobic exercise show promising results in helping a broad spectrum of symptoms. However, due to limited and inconsistent research results, the long term effects of aerobic exercise on brain health and clinical features in PD is unknown. The investigators will conduct a clinical trial to test the long term effects of aerobic exercise on the brain tissue, movement, mental functions, and driving in PD. If effective, aerobic exercise can be implemented immediately as a low cost, easily accessible treatment in PD.
Detailed Description
Parkinson's disease (PD) culminates in dementia, immobility, and death at a huge societal cost. Even early in the course, motor and cognitive dysfunction impairs instrumental activities of daily living (IADL). Non-motor symptoms due to fatigue, mood, sleep, and autonomic disorders further reduce quality of life (QoL). DTI shows progressive decline in brain tissue integrity. Usual care of PD centers on medical and surgical treatments relieve motor symptoms, but these cause side effects and lose efficacy over time. Usual treatment for non motor manifestations with pharmaceuticals (e.g., antidepressants) is symptomatic and not specific for PD. Acetylcholine esterase inhibitors exert modest symptomatic benefits on dementia, but there is no approved treatment for mild cognitive impairment. Physical Therapy is usually prescribed in later stages when mobility impairment ensues. There is no approved standard exercise regimen for PD. There is no cure or disease modifying treatment. Thus, there is a critical need for treatments that provide broad spectrum of benefits and slow PD. Preliminary research suggests that aerobic exercise has potential to meet this need. However, aerobic exercise is demanding and carries some risks. It is unknown if aerobic exercise is more beneficial than usual care in PD in long term due to gaps in the investigators knowledge about the effects of cardiorespiratory fitness (CRF) on brain tissue integrity, motor function, cognition, IADL, QoL, and disease progression. Limitations of current studies include short duration, small sample size, lack or inadequacy of controls, lack of outcome measures for cognition and IADL, and lack of biological markers to measure progression. The objective in this application is to fill the translational gap by determining the biological, clinical, and functional effects of long term aerobic exercise (LTAE) in PD. The overall hypothesis is that LTAE improves brain tissue integrity and slows down PD. The FIRST AIM is to determine the effects of LTAE on clinical features and functional abilities in PD. The investigators' prior 6-month, uncontrolled trial showed preliminary evidence that aerobic exercise improves aspects of motor function, cognition, and QoL in PD, but long term outcomes and implication for functional abilities are unknown. The investigators hypothesize that LTAE will provide sustained improvement in motor function, cognition, and non-motor symptoms with translation of benefits to QoL and IADL. The investigators will test this with a one-year randomized controlled trial (RCT) that compares the effects of moderate aerobic exercise vs usual care. The investigators will use driving as the outcome for IADL. Driving represents an important symbol for independence, and depends on integrity of cognitive and motor systems. The SECOND AIM is to determine the mechanism of LTAE effects in PD. CRF reflects complex improvements in vascular, cardiac, and metabolic health from aerobic exercise. There is preliminary evidence that higher CRF is associated with better brain health and motor/cognitive function, and that aerobic exercise improves these outcomes. For example, the investigators' preliminary study showed improvement of microtissue integrity in the striatum and white matter on DTI, but it is unclear how these changes counteract PD progression over long term. The hypotheses are: 1) LTAE will improve brain tissue integrity as indexed by DTI, 2) LTAE effects on motor and cognitive function are mediated by changes in brain tissue integrity on DTI, and 3) physiological processes leading to improved CRF from AE are critical to the benefits on the brain tissue integrity and motor/cognitive function. The investigators will test these hypotheses determining the effects of LTAE on CRF and DTI, and the association between individual differences in training related changes in motor and cognitive function, DTI, and CRF. In summary, the investigators' proposal leverages the diverse interdisciplinary team, strong preliminary data and past work, and unique infrastructure to determine if LTAE slows down neurodegeneration and clinical disability in PD.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Men or women aged 40 and older with the diagnosis of idiopathic PD per UK Brain Bank criteria
- •Hoehn-Yahr Stage I-III, on stable dopaminergic treatment regimen for equal or greater than 4 weeks prior to baseline.
- •Aerobic Fitness: VO2max below "very good" fitness levels for their age and gender at baseline cyle ergometry.
- •To include subjects who have room to improve their aerobic fitness, the investigators will enroll only those subjects whose VO2max is below "very good" fitness level (about 90% of the population) using age and gender based VO2max norms based review of 62 studies where VO2max was measured directly in healthy adult subjects in the USA, Canada and 7 European countries (Reference: Shvartz, E and Reibold, RC. Aerobic fitness norms for males and females aged 6 to 75 years: a review.
- •Aviat Space Environ Med. 1990; 61:3-11).
- •Cognitive function: No dementia per Movement Disorder Society Level I criteria (Reference: Dubois, B, Burn, D, Goetz, C, et al. Diagnostic procedures for Parkinson's disease dementia: recommendations from the movement disorder society task force. Mov Disord. 2007; 22:2314-2324).
- •Current active drivers with a valid driver's license
- •Veteran or non-veteran
Exclusion Criteria
- •Subjects unwilling or unable to give informed consent
- •Secondary parkinsonism (e.g., drug induced)
- •Parkinson-plus syndromes
- •History of brain surgery for PD such as deep brain stimulation
- •Corrected visual acuity less than 20/50 (due to effect on driving)
- •Contraindications to exercise per ACSM criteria for Exercise Testing and Training (Reference: American College of Sports Medicine. Cardiorespiratory Exercise Prescription. In: Ehrman JK, ed. ACSM's Guidelines for Exercise Testing and Prescription.6th ed. Baltimore: Lippincott Williams \& Wilkins, 2010:448-462).
- •No confounding acute or unstable medical, psychiatric, orthopedic condition. Subjects who have hypertension, diabetes mellitus, depression, or other common age related illness will be included if their disease under control with stable treatment regimen for at least 30 days.
- •Clinically significant TBI or PTSD
- •Presence of other known medical or psychiatric comorbidity that in the investigator's opinion would compromise participation in the study
- •Presence of dementia per Movement Disorder Society Level I criteria
Arms & Interventions
Aerobic
Participants randomized to aerobic exercise
Intervention: Aerobic walking
Control
Participants randomized to usual care with PD specific health education
Intervention: Usual care with PD specific health education
Outcomes
Primary Outcomes
Change in MDS-UPDRS Part III Motor (OFF) Score
Time Frame: Final Visit at 1 year - Baseline
Measures change in the severity of parkinsonism. Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS), Motor section (Part III), measured in the "practically defined" OFF state (after overnight, \~12 hours, withdrawal of PD medications). It measures specific signs like rigidity, tremor, bradykinesia (slowness of movement), and gait abnormalities by a certified rater. Each item is rated 0-4: 0 - Normal (no impairment), 1 - Slight, 2- Mild, 3 - Moderate, 4 - Severe. Total score is reported (range 0-132). Higher scores worse for individual data points. Lower value better for change score.
Change in Flanker Task
Time Frame: Final visit at 1 year - Baseline
Measures change in the executive function domains of inhibitory control and attention. Uncorrected Standard Score of the NIH Toolbox Flanker Inhibitory Control and Attention Test. The Raw Score is based on number correct × average reaction time (accuracy \& speed composite). The Uncorrected Standard Score is based on age-normed raw score with mean = 100 and SD = 15. Score range 40-160 with interpretation below: ≥ 130 - Very Superior, 115-129 - Superior, 85-114 - Average, 70-84 - Below Average, \< 70 - Impaired / markedly low attention control. Higher scores better for individual data points. Higher value better for change score.
Change in Road Safety Error Count
Time Frame: Final Visit at 1 year - Baseline
Number of safety errors made during an experimental real-world road drive test, scored by a certified driving instructor per criteria in the Iowa Department of Transportation's Drive Test Scoring Standards. Higher error count score worse. Lower scores better for change score.
Change in the Parkinson's Disease Questionnaire-39 (PDQ-39) Score
Time Frame: Final Visit at 1 year - Baseline
Questionnaire regarding activities of daily living and ability within the last month. PDQ-39 has 8 domains: Mobility (10 items) → max = 40, Activities of daily living (6 items) → max = 24, Emotional well-being (6 items) → max = 24, Stigma (4 items) → max = 16, Social support (3 items) → max = 12, Cognitions (4 items) → max = 16, Communication (3 items) → max = 12, Bodily discomfort (3 items) → max = 12. Domain Score=(Sum of item scores/Maximum possible)\*100 . The main outcome measure is PDQ-39 Summary Index (PDQ-39 SI) is the mean of the 8 domain scores (range = 0 to 100). Higher scores at datapoints are worse. Lower change score is better.
Change in Cingulum Cingulate Radial Diffusivity (rD)
Time Frame: Final Visit at 1 year - Baseline
Brain tissue integrity. Change in regional diffusion coefficient for radial diffusivity (rD) on DTI. Higher scores worse at individual data points. Lower scores better for change.
Change in Superior Longitudinal Fasciculus Radial Diffusivity (rD)
Time Frame: Final Visit at 1 year - Baseline
Brain tissue integrity. Change in regional diffusion coefficient for radial diffusivity (rD) on DTI. Higher scores worse at individual data points. Lower scores better for change.
Change in Putamen Radial Diffusivity
Time Frame: Final Visit at 1 year - Baseline
Brain tissue integrity. Change in regional diffusion coefficient for radial diffusivity (rD) on DTI. Higher scores worse at individual data points. Lower scores better for change.
Secondary Outcomes
- Change in MDS-UPDRS Non-motor Experiences of Daily Living Subscale (Part I) Score(Final Visit at 1 year - Baseline)
- Change in MDS-UPDRS Motor Experiences of Daily Living Score (Part II)(Final Visit at 1 year - Baseline)
- Change in ON Period MDS-UPDRS Motor Examination Subscale Score (Part 3)(Final Visit at 1 year - Baseline)
- Change in MDS-UPDRS Dyskinesia and Motor Fluctuations (Part 4)(Final Visit at 1 year - Baseline)
- Change in Total MDS-UPDRS Score(Final Visit at 1 year - Baseline)
- Change in 2-Minute Walk Test(Final Visit at 1 year - Baseline)
- Change in 9-Hole Peg Board Test (OFF)(Final Visit at 1 year - Baseline)
- Change in 9-Hole Peg Board Test of NIH Toolbox Motor Battery (ON)(Final Visit at 1 year - Baseline)
- Change in Montreal Cognitive Assessment (MOCA)(Final Visit at 1 year - Baseline)
- Change in COGSTAT Score(Final Visit at 1 year - Baseline)
- Change in Complex Figure Test-Recall (CFT-Recall)(Final Visit at 1 year - Baseline)
- Change in Controlled Oral Word Association Task (COWA)(Final Visit at 1 year - Baseline)
- Change in Block Design Test (BLOCKS)(Final Visit at 1 year - Baseline)
- Change in Judgment of Line Orientation Test (JLO)(Final Visit at 1 year - Baseline)
- Change in Delayed Recall of Rey Auditory Verbal Learning Test (AVLT-Recall)(Final Visit at 1 year - Baseline)
- Change in Complex Figure Test -Copy (CFT-Copy)(Final Visit at 1 year - Baseline)
- Change in Benton Visual Retention Test (BVRT)(Final Visit at 1-year - Baseline)
- Change in Trail Making Test- A (TMT-A)(Final Visit at 1 year - Baseline)
- Change in Trail Making Test - B (TMT-B)(Final visit at 1-year - Baseline)
- Trail Making Test B-A (TMT B-A)(Final Visit at 1-year - Baseline)
- Change of Geriatric Depression Scale (GDS) Score(Final Visit at 1 year - Baseline)
- Change in Beck Anxiety Inventory (BAI) Score(Final Visit at 1 year - Baseline)
- Change in Fatigue Severity Scale (FSS)(Final Visit at 1 year - Baseline)