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临床试验/NCT03313895
NCT03313895已完成不适用

Efficacy and Mechanisms of Combined Aerobic Exercise and Cognitive Training (ACT) in MCI

Arizona State University8 个研究点 分布在 1 个国家目标入组 146 人开始时间: 2018年7月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
146
试验地点
8
主要终点
Executive function

研究概览

简要总结

This multi-site clinical trial occurs at the University of Minnesota and University of Rochester. It tests the efficacy and additive/synergistic effects of an ACT intervention on cognition and relevant mechanisms (aerobic fitness, Alzheimer's disease [AD] signature cortical thickness, and default mode network [DMN]) in older adults with amnestic MCI (aMCI).

详细描述

Because almost all drug trials for Alzheimer's disease (AD) have failed, developing non-pharmacological interventions with strong potential to prevent or delay the onset of AD in high-risk populations (e.g., those with mild cognitive impairment [MCI]) is critically important. Aerobic exercise and cognitive training are 2 promising interventions for preventing AD. Aerobic exercise increases aerobic fitness, which in turn improves brain structure and function, while cognitive training improves selective neural function intensively. Hence, combined Aerobic exercise and Cognitive Training (ACT) may very well have an additive or synergistic effect on cognition by complementary strengthening of different neural functions. Few studies have tested ACT's effects, and those studies have reported discrepant findings, largely due to varying ACT programs. The purpose of this single-blinded, 2×2 factorial Phase II randomized controlled trial (RCT) is to test the efficacy and additive/synergistic effects of a 6-month combined cycling and speed of processing (SOP) training intervention on cognition and relevant mechanisms (aerobic fitness, AD signature cortical thickness, and functional connectivity in the default mode network [DMN]) in older adults with amnestic MCI (aMCI).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • A clinical diagnosis of MCI
  • Community-dwelling
  • Age 65 years and older
  • English-speaking
  • Adequate visual acuity
  • Verified exercise safety by medical provider
  • Stable on drugs affecting cognitive and psychological status
  • Verified MRI safety
  • Capacity to consent

排除标准

  • Geriatric Depression Scale < 5
  • Resting heart rate (HR) ≤50 due to arrhythmia or ≥100 beats/min
  • Neurological (e.g., dementia, head trauma), psychiatric (e.g., bipolar, schizophrenia, or depression), or substance dependency (alcohol or chemical dependency) in the past 5 years that are the main contributor to MCI
  • Contraindications to exercise, e.g. unstable angina, recent surgery
  • New symptoms or diseases that have not been evaluated by a health care provider
  • Current enrollment in another intervention study related to cognitive improvement (reduce confounding effects on outcomes)
  • Abnormal MRI findings

结局指标

主要结局

Executive function

时间窗: Change from baseline to 3, 6, 12, and 18 months

EXAMINER

Episodic memory

时间窗: Change from baseline to 3, 6, 12, and 18 months

RAVLT and BVMTR

AD-signature cortical thickness

时间窗: Change from baseline to 6, 12, and 18 months

Magnetic Resonance Imaging (MRI)

Functional connectivity in DMN

时间窗: Change from baseline to 6, 12, and 18 months

Functional MRI for Default Mode Network

Aerobic fitness

时间窗: Change from baseline to 3, 6, 12, and 18 months

VO2peak from symptom-limited peak cycle-ergometer test, and 10-m Incremental Shuttle Walk Test

Conversion to Alzheimer's disease

时间窗: Change from baseline to 6, 12, and 18 months

Clinical adjudication of Alzheimer's disease dementia

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (8)

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