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临床试验/NCT04796506
NCT04796506招募中不适用

Slow Wave Sleep As a Biomarker of Rehabilitation-induced Cognitive Improvement in Parkinson's Disease R01 HD100670

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2021年7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
招募中
入组人数
120
试验地点
1
主要终点
Change in Cognition in Stroop inhibition

研究概览

简要总结

The purpose of this study is to investigate the effects of exercise rehabilitation on cognition and to evaluate slow wave sleep (SWS) as a biomarker and mediator of response to rehabilitation-induced improvement in cognitive performance among persons with Parkinson's disease (PwP), with the ultimate goal of maximizing rehabilitation efficacy at the individual level (i.e. precision rehabilitation).

详细描述

Sleep impairment adversely affects cognitive function and increases risk for dementia. Slow wave sleep (SWS) or delta sleep (non-rapid eye movement (REM) stage 3; N3) is especially important for cognition due to its association with synaptic plasticity, synaptic potentiation, synaptic renormalization, and cortical reorganization, especially in prefrontal cortex. Clinically, SWS contributes to memory consolidation and language performance. The investigators have previously shown that the amount of SWS in persons with Parkinson's disease (PwP) is related to cognitive performance, especially in the domain of executive function. The investigators have also shown that exercise increases SWS in some PwP and that participants who have an exercise-induced increase in SWS also have improvement in executive function. This study will evaluate changes in cognitive function and SWS due to progressive resistance training rehabilitation (PRT). Participants who do not have an increase in SWS with PRT (non-responders) over 12 weeks will be transitioned to an endurance training (ET) intervention, while those who do have an increase in SWS (responders) will continue in PRT for an additional 12 weeks.

研究设计

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

盲法说明

Interpretation of polysomnography and cognitive performance will be blinded to intervention assignment.

入排标准

年龄范围
45 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •clinical diagnosis of idiopathic PD, based on the presence of bradykinesia as well as at least one of the following: rest tremor, rigidity, and/or postural instability (per United Kingdom PD Brain Bank Criteria)
  • •Hoehn and Yahr stage 2-3 (performed at screening visit)
  • •age ≥ 45 and
  • •on stable medications for at least 4 weeks prior to study entry without expecting to change medications for the duration of the study.
  • •Montreal Cognitive Assessment (MoCA) score ≥ 18 and <26 (performed at screening visit)
  • •No contraindications to an exercise program.

排除标准

  • •fails exercise readiness evaluation at screening visit
  • •regular participation in an exercise program
  • •cardiovascular or pulmonary disease, including uncontrolled hypertension, congestive heart failure, unstable coronary artery disease, serious arrhythmia, stroke within the past year, or chronic obstructive pulmonary disease (COPD)
  • •shift workers
  • •signs indicative of atypical Parkinsonism (cerebellar signs, supranuclear gaze palsy, apraxia, prominent autonomic failure, or other cortical signs)
  • •secondary Parkinsonism (neuroleptic treatment at time of onset of Parkinsonism or at time of study entry, history of multiple strokes with stepwise progression of Parkinsonism, or history of multiple head injuries)
  • •inability to walk without assistance
  • •deep brain stimulation (DBS)
  • •known narcolepsy
  • •untreated sleep apnea
  • •any condition that, in the opinion of the investigator, will preclude the participant from successfully or safely completing study procedures.

研究组 & 干预措施

Exercise Group

Active Comparator

PD participants randomized to progressive resistance training PRT) will have 12 weeks of supervised PRT 3 times per week. After the 1st 12 weeks, responders to PRT (increase in slow wave sleep) will continue PRT for an additional 12 weeks, non-responders to PRT will transition to endurance training (ET).

干预措施: Progressive Resistance Training (PRT) (Other)

Exercise Group

Active Comparator

PD participants randomized to progressive resistance training PRT) will have 12 weeks of supervised PRT 3 times per week. After the 1st 12 weeks, responders to PRT (increase in slow wave sleep) will continue PRT for an additional 12 weeks, non-responders to PRT will transition to endurance training (ET).

干预措施: Endurance Training (ET) (Other)

Delayed Exercise Group

Placebo Comparator

PD participants randomized to the delayed exercise control group will not exercise for the 1st 12 weeks of the study. After the 1st 12 weeks, participants in the delayed exercise group will transition to PRT for the 2nd 12 weeks.

干预措施: Progressive Resistance Training (PRT) (Other)

Delayed Exercise Group

Placebo Comparator

PD participants randomized to the delayed exercise control group will not exercise for the 1st 12 weeks of the study. After the 1st 12 weeks, participants in the delayed exercise group will transition to PRT for the 2nd 12 weeks.

干预措施: Delayed Exercise Training (DE) (Other)

结局指标

主要结局

Change in Cognition in Stroop inhibition

时间窗: Baseline to twelve weeks

Change in executive function on the Stroop inhibition

次要结局

  • Change in slow wave sleep (SWS)(Change from baseline to twelve week and change from twelve weeks to 24 weeks.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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