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临床试验/NCT01740128
NCT01740128已完成不适用

A Hebbian Approach to Regaining Control of Spared Circuits in Spinal Cord Injury

VA Office of Research and Development2 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2013年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
21
试验地点
2
主要终点
Change in Motor Evoked Potential (MEP) Amplitude in the Tibialis Anterior Muscle at the End of Training.

研究概览

简要总结

Many people with spinal cord injury (SCI) retain at least some movement below their injury, but their muscles often have a 'mind of their own'. Typical exercise programs focus on keeping muscles strong and flexible, but don't usually focus on helping patients control their muscles. The investigators' exercise research study will compare two different programs with the specific goal of improving conscious control of patients' muscles below the injury. This study focuses on those with 'chronic' SCI - the injury occurred at least one year prior to enrolling.

This is a single center study taking place in the Bronx, NY.

The first phase of the study will be observational - the investigators will analyze which nerve connections might remain partially intact through the injury (even if the nerves aren't consciously controlled). Participants with all severity of SCI may participate in this first phase.

The second phase of the study will involve people who retain at least slight ability to move their legs and the ability to move the arms against gravity. Each person will undergo two different exercise rehabilitation strategies: weight-supported treadmill training; and balance training combined with skilled arm or hand exercises.

The investigators will compare the effects of these exercise programs on a variety of outcomes, including gait speed, balance, strength, and muscle activation in response to brain stimulation.

The investigators hypothesize that participants with chronic SCI undergoing combined balance/arm/hand training will show improved outcomes when compared to traditional gait or balance training.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
21 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Males or females age 21-65 years;
  • SCI duration > 12 months;
  • SCI level C2-T12;
  • All SCI severity eligible for baseline testing;
  • For exercise protocol, must have severity of Grade C or D on American Spinal Injury Association (ASIA) Impairment Scale, or volitional strength of at least 1/5 in two or more key lower extremity muscles, as well as at least 3/5 in both shoulder and elbow muscles;
  • Able to tolerate upright position with support;
  • Morphologically capable of fitting a weight-support harness and robotic treadmill system;
  • Ability to give informed consent.

排除标准

  • Unsuitable cognitive capacity as judged by the study physician;
  • Diagnosis of neurological injury other than SCI, such as stroke, traumatic brain injury, or other neurological condition that the study physician considers to be exclusionary;
  • Multiple spinal cord lesions;
  • History of frequent autonomic dysreflexia;
  • History of seizures;
  • Use of medications that significantly lower seizure threshold, such as anti-psychotics, tricyclic antidepressants, amphetamines, and bupropion;
  • History of implanted brain/spine/nerve stimulators, aneurysm clips, or cardiac pacemaker/defibrillator;
  • Deep vein thrombosis in lower extremities of less than 6 months duration;
  • Pregnancy;
  • (Interventional phase only): Lack of detectable tibialis anterior motor evoked potential (MEP) at baseline even with active facilitation;
  • (Interventional phase only): Pressure ulcers greater than stage 1 severity on the foot, ankle, knee and/or pelvic girdle;
  • (Interventional phase only): Bone mineral density of the hip (proximal femur) T-score <3.5 standard deviations from age- and gender-matched normative data;
  • (Interventional phase only): Any spasticity, contractures, or heterotopic ossification that result in inadequate range of motion of the shoulder, elbow, wrist, fingers, hip, knee, or ankle joints in the judgment of the study physician;
  • (Interventional phase only): Inability to cooperate with instructions or unwilling to commit to daily training sessions for 3-4 days per week over 12-16 weeks;
  • (Interventional phase only): A diagnosis of coronary artery disease that precludes moderate to intense exercise.

研究组 & 干预措施

Multimodal then Treadmill training

Experimental

Participants will undergo harness-supported multimodal balance training exercises while simultaneously performing skilled hand exercises. Following a washout period of at least 6 weeks, Participants will undergo body weight supported treadmill training using the Lokomat apparatus.

干预措施: Robotic body weight supported treadmill training (Device)

Multimodal then Treadmill training

Experimental

Participants will undergo harness-supported multimodal balance training exercises while simultaneously performing skilled hand exercises. Following a washout period of at least 6 weeks, Participants will undergo body weight supported treadmill training using the Lokomat apparatus.

干预措施: Harness-supported multimodal balance training (Other)

Treadmill then Multimodal training

Active Comparator

Robotic body weight supported treadmill training will be applied using the Lokomat apparatus. Following a washout period of at least 6 weeks, Participants will undergo harness-supported balance training exercises while simultaneously performing skilled hand exercises.

干预措施: Robotic body weight supported treadmill training (Device)

Treadmill then Multimodal training

Active Comparator

Robotic body weight supported treadmill training will be applied using the Lokomat apparatus. Following a washout period of at least 6 weeks, Participants will undergo harness-supported balance training exercises while simultaneously performing skilled hand exercises.

干预措施: Harness-supported multimodal balance training (Other)

结局指标

主要结局

Change in Motor Evoked Potential (MEP) Amplitude in the Tibialis Anterior Muscle at the End of Training.

时间窗: Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months)

Change between baseline and Evaluation #2 in motor evoked potential area in the tibialis anterior muscle.

次要结局

  • Change From Baseline in Berg Balance Scale Sitting With Back Unsupported Score.(Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months))
  • Change From Baseline in Walking Index for Spinal Cord Injury II (WISCI II) Scale.(Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months))
  • Change in Gait Speed on 10-meter Walk Test.(Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months))
  • Changes From Baseline in Survey: Spinal Cord Injury - Spasticity Evaluation Tool (SCI-SET)(Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months))
  • Change in Leg Spasticity on Modified Ashworth Scale(Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months))
  • Change From Baseline in Soleus H-reflex Facilitation.(Time Frame: Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months))
  • Change From Baseline in ISNCSCI Lower Extremity Motor Score.(Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months))
  • Change From Baseline in Endpoint Excursion and Directional Control Parameters Achieved During Seated Limits of Stability Testing.(Time Frame: Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months))
  • Change From Baseline in Total Number of Steps Taken by Both Feet During Seated 10-second Step Test.(Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months))
  • Change in Subjective Pain as Determined by McGill Pain Questionnaire (Short Form).(Eval #1 at baseline; Eval #2 at end of training (48 sessions, average 3-4 months))

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (2)

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