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临床试验/NCT01294332
NCT01294332已完成1 期

Effect of Aerobic Exercise Training on Cardiorespiratory Fitness in Patients With Traumatic Brain Injury

National Institutes of Health Clinical Center (CC)1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2011年5月26日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
13
试验地点
1
主要终点
Change in peak oxygen consumption

研究概览

简要总结

Background:

- Many people who have traumatic brain injury (TBI) have low levels of physical fitness. Low physical fitness causes severe fatigue that reduces the ability to perform routine daily activities, and may also cause increased depression, anxiety, or sadness. Aerobic exercise, such as treadmill walking or running, improves physical fitness in most people and may also decrease fatigue and improve mood. However, more information is needed to determine if exercise improves these conditions in people who have TBI.

Objectives:

- To examine the effect of an aerobic treadmill walking exercise program on physical fitness, fatigue, and mood in people with TBI.

Eligibility:

- Individuals between 21 and 45 years of age who had a nonpenetrating traumatic brain injury at least 6 months before participating; able to understand oral and written English language, give informed consent and sign a consent form; are physically inactive (including activities related to both job and recreation); and are able to stand and walk on a treadmill safely without help.

Design:

  • This study requires 4 testing visits and 36 exercise visits over 14 weeks.
  • The first and third testing visits will last about 4 hours and the second and final testing visits will take about 2 hours.
  • Testing visits will consist of a medical history and physical examination, completion of questionnaires (about fatigue, daily physical activity, sleep quality, mood, and overall quality of life), tests of thinking and a treadmill exercise test.
  • Participants will have treadmill exercise training 3 days per week for 12 weeks. Each session includes a check-in, warm-up, treadmill walking at the training heart rate, and cool-down. Thirty-two of the sessions will last for about 1 hour, and four of the sessions will include questionnaires to fill out and will last about one-and-a-half hours.
  • After completing the exercise training program, participants will have a final testing visit to complete the questionnaires (about fatigue, daily physical activity, sleep quality, mood, and overall quality of life), tests of thinking and a treadmill exercise test.

详细描述

Objective

The broad objective of this exploratory project is to inform clinical studies and trials on the use of aerobic exercise training (AET) as an intervention for improving cardiorespiratory fitness in patients with traumatic brain injury (TBI). AET-induced adaptation of cardiorespiratory fitness and fatigue severity will be characterized, and time-course for changes in mood reactivity will be determined. We hypothesize that 1) AET will improve both cardiorespiratory fitness and fatigue severity 2) mood will at first worsen in response to AET but that mood reactivity will then decrease at some point during the intervention, and 3) AET will not impair overall cognitive performance, but that the specific cognitive performance areas of attention and concentration will improve with AET.

Study Population

Thirty-six adult subjects with a clinical diagnosis of non-penetrating TBI (mild, moderate, and severe) will be enrolled. Subjects will be recruited from NIH, affiliated hospitals/clinics, and in the community.

Design

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

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

入选标准

  • INCLUSION CRITERIA:
  • Subjects eligible for participation in this research study must meet the following inclusion criteria:
  • Diagnosis of non-penetrating mild, moderate, or severe TBI
  • Injury occurred at least 6 months prior to enrollment
  • Age 21-45 years
  • Physically inactive as identified by a physician.
  • Able to stand and walk on a treadmill independently and safely without assistance
  • Able to follow the study protocol
  • Fluent in English and able to provide informed consent
  • Willing and safely able to forego starting or changing an exercise program or treatments that would potentially alter cardiorespiratory capacity or ability to exercise and/or treatment for mood disorders

排除标准

  • Subjects are not eligible for participation in this research study if any of the following medical conditions that would impair aerobic capacity or the ability to engage in physical activity exist, including diseases of the cardiovascular (other than hypertension controlled by medication to below 140/90 mmHg), pulmonary, neurological, metabolic, or musculoskeletal systems such as:
  • Diagnosis or history of ischemic heart disease, including those with CABG and PTCA
  • Dilated or hypertrophic cardiomyopathy
  • Non-idiopathic cardiomyopathy
  • Uncontrolled hypertension, defined as a resting blood pressure above 140/90 mmHg
  • Diagnosis or history of right or left-sided heart failure or pulmonary hypertension
  • Diagnosis or history of restrictive or obstructive lung disease
  • Diagnosis or history of stroke
  • Type I or Type II Diabetes Mellitus
  • Diagnosis of chronic kidney disease, chronic liver disease, acute kidney injury or acute liver failure
  • Metastatic cancer active within the previous five years
  • Mitochondrial disease
  • On medications that would influence aerobic capacity, the ability to adapt to exercise training, or treadmill performance such as beta blockers or antiretroviral therapy
  • Active substance abuse including ETOH
  • Ongoing tobacco use (any use within the past six months)
  • Medical or Psychological instability such that the subject could not reasonably be expected to fulfill the study requirements
  • BMI greater than 40 kg/m(2)

研究组 & 干预措施

Exercise

Experimental

Aerobic exercise performed for 12 weeks

干预措施: Aerobic Exercise Training (Other)

结局指标

主要结局

Change in peak oxygen consumption

时间窗: Pre and post

The peak VO2 as measured by gas exchange during a cardiopulmonary exercise test to volitional exhaustion.

次要结局

未报告次要终点

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (1)

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