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临床试验/jRCT1032260226
jRCT1032260226进行中(未招募)不适用

Exploratory Study on the Effectiveness and Utility of a Smartwatch-Linked App-Based Multicomponent Exercise Program for Increasing Muscle Mass in Older Adults

未提供0 个研究点目标入组 30 人开始时间: 待定

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non Randomized

入排标准

年龄范围
60age old over 至 74age old not(—)
性别
All

入选标准

  • Participants who meet all of the following criteria will be eligible for this study:
  • Individuals who wish to participate in the 8-week program and are able to regularly attend the group exercise classes at the designated facility.
  • Men and women aged 60 to 74 years at the time of informed consent.
  • Individuals who are able to independently perform basic activities of daily living.
  • Individuals who provide written informed consent to participate in this study of their own free will.
  • Individuals who have no difficulty performing moderate-intensity exercise, such as exercise that causes slightly increased breathing, for at least 150 minutes per week.
  • Individuals who use a smartphone on a daily basis.

排除标准

  • Individuals who meet any of the following criteria will be excluded from this study
  • Individuals who have no intention of making exercise a habit, or who do not have an environment that allows them to incorporate exercise into their daily lives.
  • Individuals with any of the following diseases or conditions who have been judged by a medical institution to be unsuitable for performing exercise or similar activities
  • a. Severe cardiovascular disorders, such as myocardial infarction, or severe hypertension or diabetes mellitus.
  • b. Respiratory diseases, such as chronic obstructive pulmonary disease.
  • c. Orthopedic problems, such as bone or joint diseases.
  • d. Individuals undergoing hemodialysis.
  • e. Other diseases or conditions that are considered to affect the individual's ability to perform the exercise or similar activities required in this study.
  • Individuals who have previously been diagnosed with arrhythmia, including tachyarrhythmia, bradyarrhythmia, or atrial fibrillation, and who have been judged by a medical institution to be unsuitable for performing exercise or similar activities.
  • Individuals who are otherwise judged by the principal investigator to be inappropriate for participation in this study.

研究者

发起方
未提供

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