Personalisation of Exercise by Muscle Modulation, Step 1: Construction and Validation of an Algorithm for Personalisation for Pedalling Exercises
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 133
- 试验地点
- 1
- 主要终点
- Phase 1:level of pain measured by visual analog scale
研究概览
简要总结
The aim of the EXO-MODE project is to develop an innovative algorithm for the personalisation of Concentric and / or Eccentric training programmes adapted to the individual to improve the efficiency and tolerance. This algorithm will make it possible to personalise trainings programmes according to the different profiles of subjects, determined on the basis of their personal characteristics (age, sex, comorbidities), their exercise capacity and muscle performance, their level of motivation and their perception of the workload, and of the principal objective of the training programme. The final goal is to develop a tool to allow elderly populations to exercise more easily and more effectively.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Subject able to understand simple instructions and to provide consent
- •Men or women aged 18 to 75 years old.
- •Subjects who engage in moderate physical activity (Level 1 or 2 defined by the recommendations for the classification of subjects during performance studies) [2].
排除标准
- •Persons without national health insurance cover,
- •Cardio-respiratory failure, coronaropathy, severe obstructive cardiomyopathy,
- •Recent history of venous thromboembolism (previous 3 months),
- •Any medical disorder that could have a major impact on functional capacities (examples: non-stabilised metabolic disorders, such as progressive renal failure, severe asthenia related to a non-stabilised disease, such as neoplasia, systemic disease...),
- •Physical disability affecting the lower limbs or the pelvis that could impair or prevent exercise on a cycle ergometer, whether neurological (central or peripheral), arterial (i particular, arteriopathy of the lower limbs with a systolic index < 0.6) or orthopaedic (degenerative or inflammatory rheumatism).
- •Pregnant or breast-feeding women
研究组 & 干预措施
healthy volunteers
干预措施: pedalling exercises (Other)
结局指标
主要结局
Phase 1:level of pain measured by visual analog scale
时间窗: through study phase completion, an average of 9 months
Preliminary phase: level of perception of effort dissociated from the pain felt
时间窗: through study phase completion, an average of 3 months
次要结局
未报告次要终点