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临床试验/NCT06386536
NCT06386536Unknown不适用

Cycling for Improved Health: Development and Evaluation of TRIVEL's Smart Bike Training Prescription Programs

Sylvie Nadeau2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2024年1月15日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
10
试验地点
2
主要终点
Leg strength and endurance

研究概览

简要总结

This pilot A-B study aims to develop and validate personalized training programs for older adults with decreased mobility on a Semi-Reclining Intelligent Stationary Bike prototype.

The study also aims to assess the feasibility and acceptability of the training programs and to document their preliminary effects on physical health, perceived well-being, and quality of life. Ten participants will take part in five personalized training sessions with the intelligent bike and five standard training sessions with a traditional stationary bike.

详细描述

An intelligent stationary bike prototype (iBike) is being developed to evaluate the lower limbs' function during pedaling. The iBike uses artificial intelligence to prescribe personalized training programs based on individual pedaling data. This pilot study aims to develop the training programs, validate their prescription by the iBike, and assess their feasibility, acceptability, and preliminary effects on physical health, perceived well-being, and quality of life in older adults with decreased mobility.

First, the iBike training modules will be developed through a thorough literature review, and prescription criteria will be identified based on the users' pedaling and clinical data as well as expert opinion. Second, 10 participants' lower limb function (i.e. strength, range of motion, coordination and endurance) will be evaluated by the iBike during active and passive pedaling. The evaluation results will be used by the iBike to prescribe a personalized training program. Expert clinicians will also be provided with the ibike evaluation data and will be asked to recommend a personalized exercise program for each participant based on their data. The iBike's prescription of training programs will be validated by comparing it with that of expert clinicians. Third, the feasibility, acceptability, and preliminary effects of the iBike training programs on mobility, physical health, perceived well-being, and quality of life will be assessed through ten training sessions (twice weekly for 45 minutes) with ten older adults using an A-B study design. During the A and B phases, participants will undergo training with either the iBike or a conventional stationary bike.

Ultimately, the goal is to deploy and test this technology in various living spaces and rehabilitation environments to demonstrate its benefits on the physical activity level of healthy older adults and those with mobility problems.

研究设计

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

入排标准

年龄范围
50 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Being aged 50 and over
  • Having impaired standing mobility associated with aging and/or a stable chronic illness (> 6 months; controlled health condition, no change in medication, routine medical follow-up ; no emergency consultation episode).
  • Being able to walk without human assistance for short distances
  • Being able to tolerate 90 minutes of activities with rest.
  • Being able able to come to the research center for 13 visits, twice a week.

排除标准

  • Individuals with or at high risk of having a heart or lung condition (thoracic surgery, angina, myocardial infarction, uncontrolled high blood pressure, shortness of breath at rest).
  • Being unable to pedal on a seated stationary bike.
  • Having active treatments, including physiotherapy and occupational therapy.
  • Having moderate and severe cognitive problems (Mini-Mental State Examination (MMSE) score≤ 21/30).

结局指标

主要结局

Leg strength and endurance

时间窗: 8-9 weeks

The sit to stand test: evaluated as the number of stands a person can complete in 30 seconds. This outcome will be measured 3 times at baseline and once at the end of each phase of the trial.

Walking ability and functional capacity

时间窗: 8 to 10 weeks

2min walk test (2MWT): the participants will be asked to walk as fast as they can, safely, without assistance for two minutes. This outcome will be measured 3 times at baseline and once at the end of each phase of the trial.

次要结局

  • Quality of life(8-9 weeks)
  • Well-being(8-9 weeks)

研究者

发起方
Sylvie Nadeau
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Sylvie Nadeau

Professor

Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal

研究点 (2)

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