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临床试验/ISRCTN10576209
ISRCTN10576209已完成未知

The effect of an 8-week treatment programme using foot electrical muscle stimulator (EMS) on physical function and leg symptoms in community-dwelling older adults: a randomised controlled trial

Actegy Health Limited.0 个研究点目标入组 129 人开始时间: 2019年6月17日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
129

研究概览

简要总结

2022 Protocol article in https://pubmed.ncbi.nlm.nih.gov/36242050/ (added 17/10/2022) 2024 Results article in https://pubmed.ncbi.nlm.nih.gov/39143586/ (added 15/08/2024)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Current inclusion criteria as of 06/04/2021:
  • Community-dwelling adults aged over 65 years affected by one or more of the following symptoms:
  • 1. Heaviness in the leg.
  • 2. Cramps in the leg, mainly during the night or at rest.
  • 3. Aching in the leg.
  • 4. Tiredness in the leg.
  • Previous inclusion criteria:
  • Community-dwelling adults over the age of 65 affected by one or more of the following symptoms:
  • 1. Swelling, mainly in the lower leg, ankle or foot.
  • 2. Heaviness in the leg.
  • 3. Cramps in the leg, mainly during the night or at rest.
  • 4. Aching in the leg.
  • 5. Tiredness in the leg.

排除标准

  • 1. Significant co-morbidities such as diabetic neuropathy.
  • 2. Significant injury to the leg(s) in the last 6 months.
  • 3. Active cancer.
  • 4. Electronic implants in the body.
  • 5. People who have recently used/currently using foot EMS.
  • 6. Non-ambulant people.
  • 7. Inability to consent or communicate in English.

研究者

发起方
Actegy Health Limited.

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