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临床试验/NCT01572311
NCT01572311已完成不适用

Study of Community Based Dual Task and Aerobic Exercise Intervention on Cognition and Mobility in Older Adults Without Dementia

Parkwood Hospital, London, Ontario2 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2012年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
44
试验地点
2
主要终点
Global cognitive functioning

研究概览

简要总结

The investigators proposed research will establish whether combining aerobic exercise with cognitive challenges is feasible and effective in community dwelling older adults with early signs of cognitive impairment.

详细描述

To determine the effects of dual-task aerobic exercise training on community dwelling older adults with early signs of cognitive impairment. We will compare an exercise intervention (E-I) versus an exercise control (E-C) group. Each week, both groups will accumulate a minimum of 120 minutes of exercise (target 150 minutes) from community-based group classes (50 minutes of aerobic exercise) and also complete 45 minutes of beginner-level Square Stepping Exercise (SSE). The E-I group will also answer cognitively challenging questions while doing SSE (dual-task training). This study will determine whether a combined multiple modality (primary component being aerobic exercise) and dual-task exercise program is both feasible and effective for improving cognitive and mobility status, as well as vascular compliance, in older adults who may be at risk for cognitive and mobility decline.

研究设计

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

入排标准

年龄范围
55 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male/Female 55-90 years old.
  • Montreal Cognitive Assessment score ≤27
  • Preserved Instrumental Activities of Daily Living (based on Lawton-Brody Instrumental Activities of Daily Living Sale)

排除标准

  • Dementia (i.e., Mini-Mental Examination score <24 or self-reported physician diagnosis)
  • Major Depression (>=16 on the Center for Epidemiologic Studies - Depression Scale combined with clinical judgment by primary study physician)
  • Other neurological or psychiatric disorders
  • Recent history of severe cardiovascular conditions
  • Significant orthopedic conditions
  • Have blood pressure >180/100 mmHg or <100/60 mmHg
  • Unable to comprehend questionnaire material/study procedures

结局指标

主要结局

Global cognitive functioning

时间窗: 26 weeks

Four standardized domain-specific composite scores were averaged to create this standardized global cognitive functioning score (incorporates executive function, processing speed, verbal learning and memory, and verbal fluency.

次要结局

  • Global cognitive functioning(12 & 52 weeks)
  • Executive Function/Mental Flexibility(12, 26, and 52 weeks)
  • Processing Speed(12, 26 and 52 weeks)
  • Verbal Learning and Memory(12, 26 and 52 weeks)
  • Verbal Fluency(12, 26 and 52 weeks)
  • Gait variability (step length) under dual-task conditions(12, 26 and 52 weeks)
  • Gait variability (step length) under single-task conditions(12, 26 and 52 weeks)
  • Gait speed under dual-task conditions(12, 26 and 52 weeks)
  • Gait speed under single-task conditions(12, 26 and 52 weeks)
  • Double support (seconds and % gait cycle time) under dual-task conditions(12, 26 and 52 weeks)
  • Double support (seconds and % gait cycle time) under single-task conditions(12, 26 and 52 weeks)
  • Step length under dual-task conditions(12, 26 and 52 weeks)
  • Step length under single-task conditions(12, 26 and 52 weeks)
  • Carotid artery compliance(12, 26 and 52 weeks)
  • Carotid artery Intima-media thickness (IMT)(12, 26 and 52 weeks)
  • Ambulatory systolic blood pressure(12, 26 and 52 weeks)
  • Clinic systolic blood pressure(12, 26 and 52 weeks)
  • Ambulatory diastolic blood pressure(12, 26 and 52 weeks)
  • Clinic diastolic blood pressure(12, 26 and 52 weeks)
  • Total balance score(12, 26, and 52 weeks)
  • Total Falls Self-Efficacy score(12, 26, and 52 weeks)

研究者

发起方
Parkwood Hospital, London, Ontario
申办方类型
Other
责任方
Principal Investigator
主要研究者

Robert Petrella, MD

Principal Investigator

Parkwood Hospital, London, Ontario

研究点 (2)

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