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临床试验/NCT00619463
NCT00619463已完成不适用

Effects of Aerobic Exercise on Cognition, Mood and Fatigue Following TBI

Icahn School of Medicine at Mount Sinai1 个研究点 分布在 1 个国家目标入组 154 人开始时间: 2007年8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
154
试验地点
1
主要终点
Global Fatigue Index (GFI)

研究概览

简要总结

The purpose of the study is to determine the efficacy of aerobic exercise for improving cognition, mood, and fatigue after Traumatic Brain Injury (TBI) as well as examine the role of Brain Derived Neurotropic Factor (BDNF) and peripheral Vascular Endothelial Growth Factor (VEGF) as mediators of response to exercise.

详细描述

The cognitive, emotional and physical effects of TBI are well documented in the literature. Specifically, reduced cognitive functioning and depression, which are much more prevalent than in the general population, represent key challenges in the rehabilitation of persons recovering from TBI. Aerobic exercise has been shown to improve cognition and mood in the general population. Although the positive effects of exercise have been known for some time, only recently have some of the mechanisms underlying these effects been defined. One hypothesized mechanism was that exercise elevates the levels of BDNF and VEGF in the CNS. Although research examining the effects of aerobic exercise in individuals with TBI is limited, exercise has been effective in improving cognition and depression in individuals with other medical conditions, such as cancer, multiple sclerosis, fibromyalgia, dementia, chronic fatigue syndrome, chronic obstructive pulmonary disease and the elderly.

The effects of aerobic exercise on patients with TBI will be examined in this clinical trial, using a crossover design with a wait-list control. The classic crossover design has been modified to examine the effects of an additional 8 weeks of exercise, for a total 16-week intervention, in one group. Participants will be randomized into one of two conditions: Group A - immediate eight weeks of intervention followed by monitoring or Group B - monitoring followed by 8 weeks of intervention. In addition, the participants in Group B will serve as their own controls to determine if another 8 weeks of exercise, for a total of 16 weeks, is necessary for cognitive improvement.

Each person will undergo individual interviews and testing/ questionnaires aimed at measuring cognition, mood, fatigue, and life satisfaction. Blood will be drawn 2 or 3 times to monitor BDNF and VEGF levels. Assessment of cognition, mood, fatigue and life satisfaction will occur at four time points for both groups.

It is hypothesized that aerobic exercise will result in improved cognition and mood from both subjective and objective perspectives. In addition, we will explore the effect of post-TBI exercise on community participation and life satisfaction and explore personal and injury characteristics that mediate effectiveness of aerobic exercise in individuals with TBI.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Be 18 to 99
  • Have experienced a TBI as a result of a blow to the head with a loss of consciousness or a period of being dazed and confused. This must be medically documented (e.g. EMS report, hospital record, physician record).
  • Be at least six-months post-injury
  • Be English-speaking since assessments and treatment sessions will be conducted by English-speaking therapists
  • Have residential telephone service since follow up assessments may be completed via phone
  • Live within 1.5 hours of NYC to be able to participate in baseline assessment and attend treatment sessions
  • Provide written informed consent for participation
  • Be willing to complete questionnaires and interviews about mood, thinking skills, fatigue, and life satisfaction
  • Being willing to comply with protocol requirements and a schedule of exercise and assessments visits
  • Being able to take part in a treadmill-based exercise program

排除标准

  • Any medical condition in which exercising may be harmful, e.g., evidence of cardiovascular compromise including: history of acute myocardial infarction, history of coronary artery disease, unstable angina, uncontrolled hypertension, orthostatic hypotension, significant aortic valve disease, uncontrolled arrhythmia, uncompensated congestive heart failure, 3rd degree AV block without a pacemaker, active pericarditis, active myocarditis, or any evidence of pulmonary, endocrine or neurologic compromise; impaired left ventricular dysfunction; or syncopal episode within the past year
  • Any medical condition requiring treatment with beta blockers or calcium channel blockers
  • Under the age of 18 years of age
  • Any clinically significant evidence of pulmonary, endocrine or neurologic (ataxia, gait disturbance, vertigo) compromise
  • Resting pulse oxymetry of less than 95% oxygen (O2) saturation, in normal air
  • Recent diagnosis of deep vein thrombosis or pulmonary embolism
  • Active systemic illness or chronic infection that is not stable
  • Active inflammatory process that is not stable
  • Clinically significant anemia
  • Clinically significant abnormal thyroid function tests
  • Pregnant females
  • Any reason that, in the investigator's opinion, makes the person unsuitable to participate
  • Unable to physically participate in an exercise program
  • Active participation in regular aerobic exercise in the six months prior to potential enrollment.
  • Active substance abuse

结局指标

主要结局

Global Fatigue Index (GFI)

时间窗: Every 8 weeks for 24 Weeks.

Hopkins Verbal Learning Test-Revised (HVLT-R)

时间窗: Every 8 weeks for 24 weeks

Digit span subtests of the WAIS-III

时间窗: Every 8 weeks for 24 weeks

Wisconsin card sort test (WCST)

时间窗: Every 8 weeks for 24 weeks

Controlled Oral Word Association Test (COWAT)

时间窗: Every 8 weeks for 24 weeks

Blood draws for assessment of BDNF and VEGF levels

时间窗: Every 8 weeks for 24 weeks

Trail Making Tests A and B (TMT)

时间窗: Every 8 weeks for 24 weeks

Stroop Word Color Test

时间窗: Every 8 weeks for 24 weeks

Beck Depression Inventory-II ( BDI-II)

时间窗: Every 8 weeks for 24 Weeks.

次要结局

  • International Physical Activity Questionnaire (IPAQ)(Once a week)
  • Injury characteristics and demographic variables(At the beginning of the study. Week 1 of 24)
  • BISQ - Brain Injury Screening Questionnaire(At the beginning of the study. Week 1 of 24)
  • Life 3(Every 8 weeks for 24 Weeks)
  • Transition Measures(Every 8 weeks for 24 Weeks)
  • University of Rhode Island Change Assessment (URICA)(Every 8 weeks for 24 Weeks)
  • Exercise Diaries(Once a day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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