Skip to main content
Clinical Trials/NCT05357638
NCT05357638
Recruiting
Not Applicable

Physical Training for People With Parkinson's Disease and Multiple Sclerosis: Effect on Mind and Body

Amsterdam UMC, location VUmc1 site in 1 country48 target enrollmentMay 2, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parkinson Disease
Sponsor
Amsterdam UMC, location VUmc
Enrollment
48
Locations
1
Primary Endpoint
Change in anxiety and depressive symptoms
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

People with Parkinson's disease and Multiple Sclerosis experience disabling motor and non-motor symptoms, which respond insufficiently to medication. To adequately alleviate disease burden, physical training is increasing acknowledged as an assisting therapy; however, the optimal dose of exercise in unknown.

Detailed Description

Next to complex motor deficits, people with Parkinson's disease and Multiple Sclerosis experience highly disabling non-motor symptoms; for example, anxiety and depression, cognitive decline, fatigue, and sleep problems. Physical training is increasingly recognized as an assisting and, importantly, safe therapy for these patients to alleviate disease burden. However, the optimal dose (i.e., type, frequency, intensity, duration) of exercise has not yet been established. This study aims to investigate differences in response patterns of motor and non-motor symptoms, blood-based biomarkers of neuroplasticity and neurodegeneration, as well as functional brain connectivity to eight weeks of high intensity interval training \[2x/week, \~30 min/session\], continuous aerobic training \[2x/week, \~50 min/session\], or movement advice \[+3000 steps/day for 5 days/week monitored with an activity tracker\]. Frequently repeated assessment of outcomes measures will be conducted.

Registry
clinicaltrials.gov
Start Date
May 2, 2022
End Date
November 2, 2025
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Amsterdam UMC, location VUmc
Responsible Party
Principal Investigator
Principal Investigator

Dr. Erwin E. H. van Wegen

Principal Investigator, Associate Professor Neurorehabilitation

Amsterdam UMC, location VUmc

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of Parkinson's Disease (PD) or Progressive Multiple Sclerosis (MS)
  • Hoehn \& Yahr stage \<4 (PD), Expanded Disability Status Scale score \<6 (MS)
  • Anxiety and/or depressive symptoms; Hospital Anxiety and Depression Scale (HADS) score \>=8 points on HADS-A and/or HADS-D
  • Sufficient cognitive ability to understand training instructions; Montreal Cognitive Assessment score \>21 points
  • Able to participate in intensive physical training, no contra-indications for exercise
  • Stable medication regime for at least 4 weeks prior to inclusion
  • Age \>=18 years

Exclusion Criteria

  • Participation in intensive exercise program in the month prior to inclusion
  • Relapse in the month prior to inclusion (MS)
  • Symptoms indicating cardiovascular, pulmonary, or metabolic disease or cardiovascular, pulmonary, or metabolic disease which are not under control with medication
  • abnormal electrocardiography in rest

Outcomes

Primary Outcomes

Change in anxiety and depressive symptoms

Time Frame: Baseline (week 0), week 4, week 12, week 16

The effect of physical training on anxiety and depressive symptoms, measured by the Hospital Anxiety and Depression Scale

Secondary Outcomes

  • Change in daily sleep quality(Weekly assessment from baseline to week 16)
  • Change in disease severity(Baseline (week 0), week 4, week 12, week 16)
  • Change in cognitive function (i.e., ability to inhibit cognitive interference)(Baseline (week 0), week 4, week 12, week 16)
  • Change in fatigue(Baseline (week 0), week 4, week 12, week 16)
  • Change in well-being(Baseline (week 0), week 4, week 12, week 16)
  • Change in motor capacity (i.e., finger dexterity)(Baseline (week 0), week 4, week 12, week 16)
  • Change in biomarkers of neuroplasticity in blood(Baseline (week 0), week 4, week 12, week 16)
  • Change in biomarkers of neurodegeneration in blood(Baseline (week 0), week 4, week 12, week 16)
  • Change in structural brain connectivity(Week 4, week 12)
  • Change in motor capacity (i.e., walking speed)(Baseline (week 0), week 4, week 12, week 16)
  • Change in cognitive function (i.e., mental flexibility)(Baseline (week 0), week 4, week 12, week 16)
  • Change in activities of daily living(Baseline (week 0), week 4, week 12, week 16)
  • Change in brain morphology(Week 4, week 12)
  • Change in brain iron concentration in the Substantia Nigra(Week 4, week 12)
  • Change in brain neuromelanin content(Week 4, week 12)
  • Change in cognitive function (i.e., range of cognitive operations: motor speed, attention, and visuoperceptual functions)(Baseline (week 0), week 4, week 12, week 16)
  • Change in sleep quality(Baseline (week 0), week 4, week 12, week 16)
  • Change in quality of life(Baseline (week 0), week 4, week 12, week 16)
  • Change in motor capacity (i.e., lower extremity function, mobility, and fall risk)(Baseline (week 0), week 4, week 12, week 16)
  • Change in brain connectivity(Week 4, week 12)
  • Change in daily mood(Weekly assessment from baseline to week 16)
  • Change in daily anxiety(Weekly assessment from baseline to week 16)
  • Change in daily ability to concentrate(Weekly assessment from baseline to week 16)
  • Change in daily fatigue(Weekly assessment from baseline to week 16)

Study Sites (1)

Loading locations...

Similar Trials