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Parkinson's DiseasePhase 2NCT02230267

High-intensity Exercise and Fall Prevention Boot Camp for Parkinson's Disease

A Phase 2 study testing High intensity exercise and balance training in people with Parkinson's Disease, run by University of Nevada, Las Vegas at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Several animal and human epidemiologic studies have provided evidence that exercise may be neuroprotective in Parkinson's disease (PD). Exercise may forestall diagnosis and, in the case of those who have already been diagnosed with PD, it may slow the observed neurodegeneration. Read more about this study

Who is it for?
Ages 45 to 85 years
Conditions the study is for
Parkinson's Disease
What is being tested?
High intensity exercise and balance training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
27 participants
Where
1 siteUnited States
Study dates
Aug 2014to Dec 2015
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 45 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Neurologist-diagnosed idiopathic PD based on the UK PD brain bank criteria
  • Aged 45-85
  • Hoehn and Yahr stages 1-3 (mild to moderate PD)
  • Participants do not anticipate a change in medication or surgical procedures in the next 8 months of the trial (2 months for the trial and 6 for the follow-up)
  • Clearance from primary care physician to participate in the trial
  • Must be stable on PD medication and DBS for 3 months prior to trial

Who cannot join

  • Poorly controlled or unstable cardiovascular disease that precludes participation in exercise
  • Moderate-to-severe dementia using the Montreal Cognitive Assessment (MoCA). We will exclude participants with a MoCA cut off score of <26/30. This cut off value has excellent sensitivity (90%) and specificity (75%).
  • Inability to stand or walk for more than 10 minutes
  • Other significant disorders that would limit endurance exercise participation (i.e., osteoarthritis, stroke, respiratory problems, traumatic brain injury, neuromuscular disease, pain)
  • Already participating in a regular, vigorous exercise program (3X/week or more of >60% estimated maximum heart rate)
  • Participants will be excluded from the trial if they are taking any medications that interfere with heart rate response to exercise

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Nevada, Las Vegas

    Las Vegas, Nevada, 89154

Other trials in United States

About this study

Several animal and human epidemiologic studies have provided evidence that exercise may be neuroprotective in Parkinson's disease (PD). Exercise may forestall diagnosis and, in the case of those who have already been diagnosed with PD, it may slow the observed neurodegeneration. Unfortunately, because this line of research is in early stages, there is little evidence to indicate what biological mechanisms underlie the neuroprotection that is conferred with exercise. Toward this end, it is possible that an interaction between endogenous antioxidant enzymes, inflammatory processes, and reactive oxygen species may be associated with exercise improvements in PD.

One of the most common reasons for premature death in PD is falls. Several meta-analyses have concluded that exercise training programs focused on balance and/or strength training are effective at improving aspects of balance. Taken together, the current body of evidence suggests that exercise may be neuroprotective and balance/strength training may decrease the likelihood of a fall. The combination of these efficacious treatment modalities (exercise and balance/strength training) in a comprehensive treatment approach to improve PD symptoms and balance has been previously reported at relatively mild or moderate exercise intensities. Because recent research has suggested that patients with PD may benefit more from more physically intense programs, we are proposing a more aggressive approach with regard to exercise intensity and frequency in the present trial. The primary purpose of this study is to determine the feasibility and safety of a high intensity exercise approach to PD. A secondary purpose is to determine the trajectory of change in outcomes over the duration of the trial from a high intensity fall prevention program. It is hoped that a signal of efficacy will allow this trial to progress to a comparative effectiveness trial. An important innovative design element is collecting biological assays to better understand the mechanism underlying the anticipated clinical improvements.

Read more

Aim 1 is to test the feasibility of a high-intensity exercise and fall prevention boot camp (HIBC) in patients with PD by analyzing adherence and whether they achieve minimum Centers for Disease Control exercise standards (150 min/wk moderate level aerobic exercise; strengthening at least two times per week) for the duration of the trial. Aim 2 is to determine if participation in an 8-week HIBC under the direction of a physical therapist is safe for individuals with PD. Secondary Aim 3 is to determine if participation in an 8-week HIBC will produce a signal of efficacy for several physical outcomes: falls per physical activity ratio, balance efficacy, motor activity, fatigue, muscle strength, bone health, cognition/mood, and quality of life. Secondary Aim 4 is to determine if participation in an 8-week HIBC will produce a signal of efficacy for biological outcomes, anti-inflammatory cytokines and anti-oxidant enzymes. An additional exploratory aim will be an analysis of BDNF val66val, val66met, met66met polymorphisms to determine if there is a differential response to exercise.

This trial is innovative because it utilizes a high intensity comprehensive exercise treatment approach (aerobic exercise, strengthening, and balance training). To our knowledge, there have been no trials of individuals with PD who have participated in a trial of this intensity in a group "boot camp" setting. Another innovative design element is the use of three novel assessments: biological assays of pro- and anti-inflammatory cytokines, endogenous anti-oxidant enzymes and a novel assessment of falls (falls per physical activity ratio).

Participants will be randomly assigned into either an 8-week HIBC group or an 8-week usual care control group (standard, low intensity group therapy class) under the direction of physical therapists. Each group will have 15 participants with a 1:5 patient-to-therapist ratio. The HIBC will be 1.5 hours daily, Monday through Friday. Participants will be required to attend 3 out of the 5 days. The protocol of the HIBC will include the following exercise components: A. 30 minutes of moderate-high intensity aerobic exercise; B. 15 minutes of strengthening the major muscle groups; C. 15 minutes of balance training; and, D. 15 minutes of interspersed rest and stretching. Participants will rotate through these four exercise components. Participants will have one baseline test and assessments at the 2-week, 4 week, 8-week, and 6-month points. Outcomes of the primary aims (Aim 1 and Aim 2) will be frequency counts of participation, adverse events, and compliance with exercise. The outcomes for the secondary aims will include measures of balance and falls, physical capacity, fatigue, exercise/physical activity behavior, and biological assays.

Being tested
High intensity exercise and balance training, Usual care arm exercise
Keywords
boot camp, exercise, balance training, fall prevention, falling, strength training
Medical subject headings
Parkinson Disease, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • High intensity exercise and balance trainingOther

    Also called A. 30 minutes of moderate-high intensity aerobic exercise at 70%+ of estimated maximum heart rate, B. 15 minutes of strengthening the major muscle groups of the trunk and upper/lower extremities, C. 15 minutes of balance training, D. 15 minutes of rest and stretching

  • Usual care arm exerciseOther

    Also called 10 minutes of stretching, 10 minutes of aerobic exercise (60% of heart rate maximum), 10 minutes of strengthening

Study groups in NCT02230267
Study groupRoleWhat they receive
High intensity boot campExperimentalEach of the two HIBCs will have 10 participants (20 total) with a 1:5 physical therapist-to-patient ratio. Each HIBC session will last 1.5 hours and will be held on 4 days of the week. Participants will be required to attend 3 of those 4 days but may attend all. Because this is a pragmatic trial, therapists will have some leeway to control the intensity and the modality of the exercise. However, the basic format of the HIBC will consist of the following exercise components: A. 30 minutes of moderate-high intensity aerobic exercise at 70%+ of estimated maximum heart rate; B. 15 minutes of strengthening the major muscle groups of the trunk and upper/lower extremities; C. 15 minutes of balance training; and, D. 15 minutes of rest and stretching. Participants will rotate through these four different exercise components in a circuit fashion.
Receives: Other: High intensity exercise and balance training
Usual care armActive comparatorThe low intensity exercise group will participate in the Fitness Counts Exercise Program (FCEP) which is a basic low intensity, sitting and standing exercise program (10 minutes of stretching, 10 minutes of aerobic exercise (60% of heart rate maximum), and 10 minutes of strengthening). This exercise program was developed by the National Parkinson Foundation and is commonly used in PD exercise classes. The physical therapist-to-patient ratio will be 1:5. As there are two clinical sites, there will be 10 participants in each of the two boot camps (20 total). The FCEP will be 1 hour daily on four days of the week. Participants will be required to attend 3 days per week but may attend more if they are able.
Receives: Other: Usual care arm exercise

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Frequency feasibility

    The number of participants that attend and participate in the treatment at least 3 times per week for 8 weeks.

    Measured: After completion of the 8 week trial

  2. Aerobic feasibility

    The number of participants that complete at least 150 minutes per week of moderate intensity exercise (70%+ of their estimated HR maximum). This will be ascertained using heart rate monitors.

    Measured: At the end of the 8 week trial

  3. Strength feasibility

    The number of participants that participate in strengthening exercises that incorporates all the major muscle groups at least two days per week.

    Measured: At the end of the 8 week trial

  4. Compliance

    Drop-out rate and reason for drop-out will be tracked.

    Measured: At the end of the 8 week trial

  5. Safety

    Exercise-related adverse events (e.g., strains/sprains, cardiovascular events).

    Measured: Ongoing throughout the 8 week trial

  6. Motivation

    The Intrinsic Motivation Inventory (IMI) will be used to gather information about motivation.

    Measured: At 8 weeks

  7. Falls

    Falls and fall injuries in and out of boot camp will be collected.

    Measured: At the end of the 8 week trial

Secondary outcomes (19)
  1. Falls

    Falls will be tracked for 6 months after the boot camp using a falls diary. A member of the research team will call each month to interview participants about their falls. We will assess falls/fall injuries per physical activity ratio during the 6 month period following the trial and time to a fall/fall injury after the trial.

    Measured: up to 6 months

  2. Motor activity

    Physical activity will be assessed using the Physical Activity Monitoring System (PAMsys).

    Measured: up to 6 months

  3. Fatigue

    Fatigue will be assessed using the Parkinson Fatigue Scale (PFS).

    Measured: up to 6 months

  4. Strength

    This will be assessed functionally using the 30 second Sit-To-Stand Test (30STS) for muscle strength.

    Measured: up to 6 months

  5. Cognition

    Cognition will be assessed using the Montreal Cognitive Assessment (MoCA).

    Measured: up to 6 months

  6. Quality of life

    This will be assessed by using a measure of disease-specific quality of life (Parkinson's Disease Questionnaire-39 (PDQ39)).

    Measured: up to 6 months

  7. Long term behavioral change

    All participants will track their participation in exercise and physical activity using an exercise diary for 6 months following the boot camp. Participants will be called monthly to reinforce completion of the exercise diary.

    Measured: up to 6 months

  8. mini-Balance Evaluation Systems Test (mini-BESTest)

    Performance-based balance tasks.

    Measured: up to 6 months

  9. Falls self-efficacy

    Activities Specific Balance Confidence Scale (ABC)

    Measured: up to 6 months

  10. Fall Efficacy

    Self-report measurement tool: Falls Efficacy Scale (FES)

    Measured: Up to 6 months

  11. Fall catastrophization

    Self-report of fall catastrophization: Catastrophization about Falls Questionnaire (CAFS)

    Measured: Up to 6 months

  12. Physical activity

    Self-report measure physical activity: International Physical Activity Questionnaire (IPAQ)

    Measured: Up to 6 months

  13. Motor symptoms

    Unified Parkinson's Disease Rating Scale motor subscale (UDPRS III)

    Measured: Up to 6 months

  14. Fear of falling

    Self-report scale of avoidance behavior due to a fear of falling: Fear of Falls Avoidance Behavior Questionnaire (FFABQ)

    Measured: Up to 6 months

  15. Endurance

    Endurance will be assessed using the 6 Minute Walk Test (6MWT).

    Measured: Up to 6 months

  16. bone health

    Bone health will be measured using bone mineral densiometry (BMD).

    Measured: up to 6 months

  17. Mood

    Mood will be measured using the Beck Depression Inventory.

    Measured: up to 6 months

  18. Catalase

    Catalase concentrations from blood will be quantified utilizing enzyme-linked immunosorbent assays.

    Measured: Up to 6 months

  19. Cytokines

    Cytokine (TNFα, IL-6, IL-10) concentrations from blood will be quantified utilizing enzyme-linked immunosorbent assays.

    Measured: Up to 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Sep 2014 (estimated)
  2. Study startAug 2014
  3. Primary completionOct 2015
  4. Study completionDec 2015

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
27 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02230267
Sponsor's protocol ID
CTR-IN UNLVPT 2014.01
Status last verified
May 2016
First submitted
27 Aug 2014
Last updated
12 May 2016
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing High intensity exercise and balance training in people with Parkinson's Disease, run by University of Nevada, Las Vegas at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 May 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Frequency feasibility (time frame: After completion of the 8 week trial). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 May 2016.

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Clinical Trial NCT02230267 | AzTrials