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临床试验/NCT04733222
NCT04733222已完成不适用

Effect of Treadmill Slip- and Trip-perturbation Training on Falls Among Community-dwelling Older Adults: A Randomized, Controlled Trial

Aalborg University Hospital1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2021年4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
140
试验地点
1
主要终点
Fall rate

研究概览

简要总结

This parallel, randomized, controlled trial aims to quantify the effects of slip- and trip-perturbation training on fall rates collected over 12 months, compared to time-matched treadmill walking, among community-dwelling older adults (≥65 years).

A sample size calculation estimated that 140 older community-dwelling older adults (≥65 years) are needed. Following baseline measures, the recruited participants will randomly be assigned to either the perturbation or the walking group. The participants in the perturbation group will be assigned to four perturbation training sessions. The walking group will perform four treadmill walking matching the exercise time of the perturbation training. Assessment of the primary outcome, fall rates, will be conducted continuously in 12 months from randomization. When a fall is reported in the fall calendar, a telephone interview will be conducted to assess the circumstances and consequences (e.g., fall-related fractures, fall-related hospital admissions) of the falls. Moreover, assessment of physical, cognitive, and social-psychological outcomes will be made at baseline, post-test, six-month, and 12-months reassessment.

详细描述

Approximately one-third of older adults fall at least once a year, and about 10% of these falls cause serious injuries such as head injuries and fractures. In fact, falls are the most frequent cause of injuries among older adults and often lead to disability, institutionalization, and premature death.

Multiple fall prevention interventions have been examined to reduce the fall rate, and physical exercise has continuously been proven as an effective and cost-effective approach. However, traditional exercise approaches, such as balance and muscle-strengthening training, have only shown a moderate 20-25% decrease in falls and encounters issues such as poor compliance. Recently, task-specific perturbation training using an overground walkway has been shown to produce quick motor adaptations resulting in improved pro- and reactive stability. Additionally, perturbation training delivered on such walkways has decreased both laboratory-induced and real-life falls. However, overground walkways with moveable platforms and trip-board are expensive and immobile; thus, limiting the clinical feasibility.

Contrarily, perturbation training delivered on computer-controlled treadmills may serve as a more implementable substitute. Preliminary studies have shown that treadmill perturbation training produces similar dynamic stability adaptations to overground perturbation training. Furthermore, a single session of treadmill perturbation decreases the rate of laboratory-induced falls, and the ergogenic effects were retained for up to six months. However, the effects of a brief treadmill perturbation training intervention on real-life falls in community-dwelling older adults still vastly unknown.

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
None

入排标准

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

入选标准

  • •≥65 years old
  • •Community-dwelling
  • •Able to walk without a walking aid

排除标准

  • •Any of the following self-reported conditions: Any orthopedic surgery within the past 12 months, osteoporosis or history of osteoporosis-related fractures (low impact hip, spine, and wrist fracture), or progressive neurological disease (e.g., Parkinson, multiple sclerosis)
  • •An unstable medical condition that would prevent safe participation
  • •Severe cognitive impairment (a score <8 in The Short Orientation-Memory-Concentration Test)
  • •Current participation in another fall prevention trial

研究组 & 干预措施

Perturbation training

Experimental

Participants randomized to the treadmill perturbation training will initially perform three sessions performed within a week followed by a "booster"-session after six months.

干预措施: Perturbation training (Other)

Treadmill walking

Active Comparator

Participants randomized to the walking group will undergo three initial sessions within a week and a "booster"-session after six months.

干预措施: Treadmill walking (Other)

结局指标

主要结局

Fall rate

时间窗: Continuously for 12 months after the initial three training sessions

Falls are collected by daily recordings in calendar that is returned to the research group monthly

次要结局

  • Proportion of participants with at least one fall(Continuously for 12 months after the initial three training sessions)
  • Time to first fall(Continuously for 12 months after the initial three training sessions)
  • Fall-related fracture rate(Continuously for 12 months after the initial three training sessions)
  • Proportion of participants with at least one fall-related fractures(Continuously for 12 months after the initial three training sessions)
  • Number of all-cause fractures(At the 52-week follow-up)
  • Number of other fall-related injuries(Continuously for 12 months after the initial three training sessions)
  • Fall-related hospital admission rate(Continuously for 12 months after the initial three training sessions)
  • Proportion of participants with at least one hospital admission(Continuously for 12 months after the initial three training sessions)
  • Number of all-cause hospital admissions(At the 52-week follow-up)
  • Laboratory-induced falls(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Gait kinematics to perturbations(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Single-task gait(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Dual-task gait(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Single-task static balance(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Dual-task static balance(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Choice stepping reaction time(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Lower extremity physical performance(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Health-related quality of life(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Fear of Falling(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Executive function(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Frailty(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))
  • Adverse events(Week 0 (Pre-training; before the first training), week 1 (Post-training; after the third training session), week 26 (26-week follow-up; before the fourth training session), and week 52 (52-week follow-up))

研究者

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

Jens Eg Nørgaard

PhD-student, Cand.Scient.

Aalborg University Hospital

研究点 (1)

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