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临床试验/NCT05076747
NCT05076747已完成不适用

Promoting Brain Plasticity During Sub-acute Stroke: the Interactive Role of Exercise and Genotype

McGill University1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2021年6月20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
70
试验地点
1
主要终点
Intra-cortical facilitation

研究概览

简要总结

This study will investigate the impact of cardiovascular exercise on brain plasticity among patients in sub-acute stages after stroke, and whether genotype modulates the response to this intervention. Participants in the experimental group will perform cardiovascular training for 8 weeks, three times/week in addition to standard therapy, while participants in the control group will perform standard therapy only. Assessments will be performed at baseline, four weeks, and 8 weeks after training.

详细描述

Background: Research has shown that the adult human brain has an enormous plastic capacity to adapt after injury. In people who have recently experienced a stroke, interventions that promote brain plasticity in early stages after stroke can improve long-term recovery. Cardiovascular exercise is a simple strategy to increase brain plasticity and promote neural reorganization. However, there is no information about the effects of cardiovascular exercise on brain plasticity in early phases of stroke, despite the importance of this initial period for long-term recovery. Similarly, it is not known if, depending on their genetic profile, some people will be more responsive than others to this type of exercise.

Objectives: To establish whether: 1) cardiovascular exercise improves brain plasticity during the initial phases of post-stroke recovery; 2) carrying a specific form of the BDNF gene modulates the response to cardiovascular exercise.

Design: 70 participants will perform either a progressive high-intensity cardiovascular exercise program or low-intensity stretching and toning exercise program. Both groups will undergo 8 weeks of training performed 3 times per week. Assessments will be performed at the beginning, mid-point (4 weeks) and at the end of the training period (8 weeks).

Methodology: Assessments: 1) brain plasticity by measuring changes in brain excitability, a marker of brain plasticity, with non-invasive brain stimulation; 2) BDNF levels by measuring the blood concentration of this protein; 3) Genotype by identifying the subtype of BDNF gene carried by each participant; 4) Cardiorespiratory fitness by assessing the performance during a graded exercise test.

Statistical analysis: Differences between exercise and control groups on the primary endpoint of all outcomes will be analyzed with linear mixed models. Besides baseline scores, sex, age, and type of stroke (cortical or subcortical) will be included as covariates because they can affect brain plasticity and BDNF response. T1 scores will also be included to increase the efficiency of the model. The influence of genotype on changes in primary and secondary outcomes in the exercise group will be inspected with the Freedman-Schatzkin test, a powerful technique to identify mediators of change that can be used in small-scale exercise studies.

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
None

入排标准

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

入选标准

  • •Individuals 40-80 years old
  • •Who had a first-ever ischemic (cortical or subcortical) stroke confirmed by MRI/CT
  • •Who had stroke 2 to 6 weeks prior to participation
  • •With recordable motor-evoked potentials (MEPs) elicited with transcranial magnetic stimulation (TMS) from the affected hemisphere
  • •With no serious musculoskeletal or neurological conditions other than stroke
  • •With sufficient cognitive/communicative capacity to safely perform the protocols.

排除标准

  • •Hemorrhagic stroke
  • •Cognitive impairment/dysphasia affecting informed consent
  • •Concurrently enrolled in another exercise program
  • •Major psychiatric or previous neurological disease
  • •Absolute contraindications to TMS or exercise

研究组 & 干预措施

Cardiovascular training

Experimental

Cardiovascular training will comprise 4 weeks of moderate-to-vigorous continuous training followed by 4 weeks of progressive high-intensity interval training (HIIT) performed on recumbent steppers. This intervention will be performed in addition to the conventional standard therapy sessions. We will start with very moderate intensities and prepare participants for higher intensities. Introducing HIIT will allow us to use higher intensities over short bursts of exercise interspersed with periods of active rest. HIIT is more effective than continuous training to increase BDNF and we have shown that even a single bout of HIIT reduces interhemispheric imbalances in excitability and improves motor learning in chronic stroke.

干预措施: Cardiovascular training (Behavioral)

Standard Therapy

Active Comparator

Will comprise 8 weeks of the control protocol that includes regular sessions of physiotherapy, occupational therapy, and speech therapy.

干预措施: Standard Therapy (Behavioral)

结局指标

主要结局

Intra-cortical facilitation

时间窗: 8 weeks

Paired-pulse motor-evoked potentials of transcranial magnetic stimulation protocol.

Cortico-spinal excitability

时间窗: 8 weeks

Single pulse motor-evoked potentials of transcranial magnetic stimulation protocol.

Intra-cortical inhibition

时间窗: 8 weeks

Paired-pulse motor-evoked potentials of transcranial magnetic stimulation protocol.

次要结局

  • Cardiorespiratory fitness(8 weeks)
  • Brain-derived neurotrophic factor(8 weeks)

研究者

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

Marc Roig

Associate Professor

McGill University

研究点 (1)

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