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临床试验/NCT01521728
NCT01521728已完成不适用

Trial of Resistance and Endurance Exercise in Amyotrophic Lateral Sclerosis (ALS)

Johns Hopkins University8 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2012年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
8
主要终点
Resistance Exercise Tolerability

研究概览

简要总结

The first questions asked by patients with a new diagnosis of Amyotrophic Lateral Sclerosis (ALS) often include: "Does exercise help slow the progression of the disease?", "Is there any harm in exercising?", or "What type of exercise (endurance or resistance) is most appropriate?" At this time, however, there is a lack of answers for people who suffer from an illness that affects their strength above all else. Yet the beneficial effects of exercise in both healthy people as well as people with other diseases have been extensively studied and resulted in recommendations about the types of exercise that are beneficial. In this study the investigators will ask participants with ALS to exercise in one of three ways: weightlifting (resistance exercise), stationary bicycling (endurance exercise), and range of motion exercise (the current "standard of care" for ALS patients). The investigators will use several different types of tests to determine whether one type of exercise is tolerated better and is safer than another. The investigators will also collect information about how the body responds to exercise in ALS. This study will help in the development of a larger national study to understand how exercise can be combined with other treatments to potentially improve strength and alter the course of the disease.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participants with familial or sporadic ALS diagnosed as possible, laboratory-supported probable, probable, or definite according to the WFN El Escorial criteria
  • Participants who are ages 18-80, inclusive.
  • Slow Vital Capacity (SVC) must be equal to or greater than 70% of predicted value
  • ALSFRS-R score >
  • Patients who are currently on any medications must be on a stable dose for the past 30 days.
  • Participants must provide informed consent prior to completion of any study procedures.

排除标准

  • Participants who are already performing >30 min. of endurance exercise/day for ≥ 3x/week (Borg scale-- "hard" or "somewhat hard") within 30 days of screening.
  • Participants who are already performing resistance exercise ≥ 3x/week within 30 days of screening.
  • Participants with history of ALS symptoms over 5 years duration
  • Inability to obtain consent (psychiatric or dementing illness)
  • History of neuromuscular dysfunction not related to ALS
  • Patents with clinically significant ECG abnormalities
  • Uncontrolled hypertension (SBP>160 or DBP>110)
  • Recent history of angina (within the last 2 years)
  • Recent history of abnormal stress test (within the last 2 years)
  • Symptomatic severe aortic stenosis
  • Active endocarditis
  • Symptomatic heart failure
  • Respiratory
  • Subjects with a history of respiratory dysfunction not related to ALS (i.e. COPD)
  • Subjects with chronic infectious disease including HIV, hepatitis B or C.
  • History of substance abuse within the past year
  • Patients who have a history of poor compliance to medical regimens or study requirements.
  • Uncontrolled diabetes
  • Recent embolism (within the last 6 months)
  • Severe orthopedic conditions that would prohibit exercise
  • Female subjects who are pregnant or planning to become pregnant.
  • Female subjects of childbearing potential who are not practicing contraception.

结局指标

主要结局

Resistance Exercise Tolerability

时间窗: 6 months

Evaluate the tolerability of RESISTANCE exercise in ALS subjects as measured by their ability to complete a 6 month study of a resistance exercise regimen.

Endurance Exercise Tolerability

时间窗: 6 months

Evaluate the tolerability of ENDURANCE exercise in ALS subjects as measured by their ability to complete a 6 month study of an endurance exercise regimen.

次要结局

  • Vital Capacity(6 months)
  • ALS Functional Rating Scores(6 months)
  • Spasticity(6 months)
  • Fatigue(6 months)
  • Quality of Life(6 months)
  • Muscle Strength(6 months)

研究者

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

Nicholas Maragakis, MD

Associate Professor

Johns Hopkins University

研究点 (8)

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