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临床试验/NCT02230267
NCT02230267已完成2 期

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

University of Nevada, Las Vegas2 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2014年8月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
27
试验地点
2
主要终点
Falls

研究概览

简要总结

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.

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
45 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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/
  • 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

结局指标

主要结局

Falls

时间窗: At the end of the 8 week trial

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

Safety

时间窗: Ongoing throughout the 8 week trial

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

Aerobic feasibility

时间窗: At the end of the 8 week trial

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.

Strength feasibility

时间窗: At the end of the 8 week trial

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

Compliance

时间窗: At the end of the 8 week trial

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

Motivation

时间窗: At 8 weeks

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

Frequency feasibility

时间窗: After completion of the 8 week trial

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

次要结局

  • Fatigue(up to 6 months)
  • mini-Balance Evaluation Systems Test (mini-BESTest)(up to 6 months)
  • bone health(up to 6 months)
  • Mood(up to 6 months)
  • Cytokines(Up to 6 months)
  • Falls(up to 6 months)
  • Motor activity(up to 6 months)
  • Physical activity(Up to 6 months)
  • Cognition(up to 6 months)
  • Quality of life(up to 6 months)
  • Falls self-efficacy(up to 6 months)
  • Fall catastrophization(Up to 6 months)
  • Endurance(Up to 6 months)
  • Fall Efficacy(Up to 6 months)
  • Strength(up to 6 months)
  • Long term behavioral change(up to 6 months)
  • Motor symptoms(Up to 6 months)
  • Fear of falling(Up to 6 months)
  • Catalase(Up to 6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Merrill Landers

Chair and Associate Professor

University of Nevada, Las Vegas

研究点 (2)

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