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NCT04284436Active, not recruiting

Study in Parkinson Disease of Exercise

Study in Parkinson Disease of Exercise Phase 3 Clinical Trial: SPARX3

Source: ClinicalTrials.gov · Last updated 10 Jul 2026

Brief summary (registry, in English)

This study is a Phase 3 multi-site, randomized, evaluator-masked, study of endurance treadmill exercise on changes in the Movement Disorder Society-Unified Parkinson Disease Rating Scale (MDS-UPDRS) Part III score at 12 months among persons with early stage Parkinson disease. 370 participants will be randomly assigned to 2 groups: 1)60-65% HRmax or 2)80-85% HRmax 4 times per week. The primary objective is to test whether the progression of the signs of Parkinson's disease is attenuated at 12 months in among persons who have not initiated medication for Parkinson Disease (PD) when they perform high-intensity endurance treadmill exercise.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
370 (actual)
First submitted
20 Feb 2020
Start date
30 Aug 2021
Primary completion date
31 Jul 2027
Lead sponsor
Northwestern University
NCT number
NCT04284436

What you commit to

  • Study type: Interventional
  • Participants enrolled: 370
  • From 30 Aug 2021 to the primary completion date, 31 Jul 2027
  • 25 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Currently being treated with PD medications such as levodopa or dopamine receptor agonists, monoamine oxidase-B (MAO-B) inhibitors, amantadine, or anticholinergics.
  • Expected to require treatment with medication for PD in the first 6 months of the study.
  • Use of any PD medication 60 days prior to the baseline visit including but not limited to levodopa, direct dopamine agonists, amantadine, Rasagiline (Azilect), Selegiline (Eldepryl), Artane (trihexyphenidyl).
  • Duration of previous use of medications for PD exceeds 60 days.
  • Use of neuroleptics/dopamine receptor blockers for more than 30 days in the year prior to baseline visit, or any use within 30 days of baseline visit
  • Recent use of psychotropic medications (e.g., anxiolytics, hypnotics, benzodiazepines, antidepressants) where dosage has not been stable for 28 days prior to screening.
  • Use of the following within 90 days prior to the DAT neuroimaging screening evaluation: modafinil, armodafinil, metoclopramide, alpha-methyldopa, methylphenidate, reserpine, any amphetamine or amphetamine derivative, or use of buproprion within 8 days prior to the DAT neuroimaging screening evaluation. These can compromise DaTscan™ SPECT.

Other illness

  • Uncontrolled hypertension (resting blood pressure \>150/90 mmHg)
  • Serious illness (requiring systemic treatment and/or hospitalization) within the last 4 weeks.
  • Beck Depression Inventory II (BDI) score \> 28, indicating severe depression that precludes ability to exercise. Any subject with such a score will be referred to a PCP or physician for further evaluation and management of depression. Individuals with a BDI-II score of 17-28 will be excluded if any of the following conditions are met: (1) individual is suicidal, (2) is in need of depression treatment modification currently or (3) depressive symptoms likely to interfere with adherence to study protocol. Any subject with such a score will be referred to a PCP or physician for further evaluation and management of depression.
  • Known allergy to iodinated products.
  • Known hypersensitivity to DaTscan™ SPECT (either to the active substance of 123I-ioflupane or any of the excipients.
  • Other disorders, injuries, diseases, or conditions that might interfere with ability to perform endurance exercises (e.g. history of stroke, respiratory problems, traumatic brain injury, orthopedic injury, or neuromuscular disease).

Lab values

  • Presence of known cardiovascular, metabolic, or renal disease or individuals with major signs or symptoms suggestive of cardiovascular, metabolic, or renal disease without medical clearance to participate in the exercise program.
  • Hypo- or hyperthyroidism (TSH \<0.5 or \>5.0 mU/L), abnormal liver function (AST or ALT more than 2 times the upper limit of normal), abnormal renal function (estimated glomerular filtration rate (eGFR) using the MDRD4 equation or the CKD-EPI equation \<45mL/min/1.73m2 ).
  • Complete Blood Count (CBC) out of range and physician's judgment that abnormal value is clinically significant.
  • Any other clinically significant medical condition, psychiatric condition, drug or alcohol abuse, assessment or laboratory abnormality that would, in the judgment of the investigator, interfere with the subject's ability to participate in the study.

Other

  • Individuals with orthostatic hypotension and standing systolic BP below 100 will be excluded. Orthostatic hypotension (OH) is a reduction of systolic blood pressure of at least 20 mm Hg or diastolic blood pressure of at least 10 mm Hg within 3 minutes of standing.
  • Montreal Cognitive Assessment (MoCA) score of \<24.
  • Individuals who have been exercising at greater than moderate intensity for 120 minutes or more per week consistently over the last 6 months will be excluded. Greater than moderate intensity is defined as a range greater than 60-65% HRmax. These individuals are excluded since their exercise activities are greater than the activities they would experience if they were assigned to the 60-65% treatment group. As such, they would be expected to lose fitness.
  • (For women only) Actively breast-feeding an infant, and/or pregnant, or plan to become pregnant in the next 12 months.

Who the study is looking for

  • A diagnosis of idiopathic Parkinson Disease based on the modified \* United Kingdom (UK) PD brain bank criteria and which are consistent with recent criteria proposed for clinically established early established Parkinson's disease that no longer exclude individuals with a family history of Parkinson's disease.
  • Hoehn and Yahr stages less than 3
  • Disease duration: less than 3 years since disease diagnosis
  • Age 40-80 years
  • Positive DaTscan™ SPECT by quantitative readout for idiopathic Parkinson disease.

Age in the registry: 40 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (25)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Alberta
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EdmontonCanadaUnknown status
Iowa State University
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AmesUnited StatesUnknown status
University of Michigan
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Ann ArborUnited StatesUnknown status
Emory University
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AtlantaUnited StatesUnknown status
Morehouse School of Medicine
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AtlantaUnited StatesUnknown status
University of Colorado Denver
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AuroraUnited StatesUnknown status
Louisiana State University
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Baton RougeUnited StatesUnknown status
University of Alabama at Birmingham
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BirminghamUnited StatesUnknown status
Boston University (Charles River Campus)
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BostonUnited StatesUnknown status
Northwestern University
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ChicagoUnited StatesUnknown status
Rush University Medical Center
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ChicagoUnited StatesUnknown status
University of Cincinnati
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CincinnatiUnited StatesUnknown status
Cleveland Clinic
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ClevelandUnited StatesUnknown status
Ohio Health
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ColumbusUnited StatesUnknown status
University of Florida
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GainesvilleUnited StatesUnknown status
Kent State University
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KentUnited StatesUnknown status
University of Minnesota
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MinneapolisUnited StatesUnknown status
Columbia University Medical Center
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New YorkUnited StatesUnknown status
University of Pennsylvania
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PhiladelphiaUnited StatesUnknown status
University of Pittsburgh
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PittsburghUnited StatesUnknown status
Oregon Health Science University
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PortlandUnited StatesUnknown status
University of Utah
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Salt Lake CityUnited StatesUnknown status
UT Health San Antonio
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San AntonioUnited StatesUnknown status
University of California San Francisco
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San FranciscoUnited StatesUnknown status
Washington University St. Louis
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St LouisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.