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临床试验/NCT06906523
NCT06906523进行中(未招募)不适用

Blood Flow Restriction in Older Adults. A Randomised Single-blind Clinical Trial

Universidad Católica San Antonio de Murcia1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2025年3月12日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
18
试验地点
1
主要终点
Change from baseline muscle power after treatment and at four weeks

研究概览

简要总结

Introduction. From the age of 80 onwards, more than 50% of people suffer from sarcopenia. The loss of muscle strength leads to a loss of muscle power, impairing functionality and preventing the correct performance of activities of daily living.

Objective. To analyse the efficacy of blood flow restriction in older adult patients by evaluating changes in the variables muscle power and strength, physical condition and functionality of the lower limbs.

Material and method. Randomised single-blind clinical study. Thirty-six older adults will be recruited and randomised to the experimental and control groups. The intervention will have a duration of 4 weeks, with 2 weekly sessions. The intervention will consist of an intervention by performing 3 quadriceps strength exercises, with a 40% restriction. The primary variable of the study will be muscle power (Sit To Stand 5 times) and the secondary variables will be muscle strength (dynamometry), physical condition (Timed Up and Go) and functionality and autonomy (Barthel index)

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
Single (Outcomes Assessor)

入排标准

年龄范围
65 Years 至 80 Years(Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Older adults aged 65 to 80 years
  • •Independent for standing and walking with the help of assistive devices such as cane and walker
  • •Both genders
  • •Normotensive or hypertensive with controlled BP (systolic blood pressure <140 mmHg)
  • •Sign the informed consent form.

排除标准

  • •People dependent for the performance of activities of daily living.
  • •People with cognitive impairments that limit the performance of the intervention or assessments.
  • •Persons undergoing total hip or knee arthroplasty
  • •Persons receiving physiotherapy treatment at the time of the study
  • •History of deep vein thrombosis (DVT) or pulmonary embolism
  • •History of myocardial infarction or stroke

研究组 & 干预措施

No intervention

No Intervention

Patients included in the control group will not receive any intervention, maintaining their activities of daily living in the same way as before the study.

Blood flow restriction

Experimental

An exercise protocol will be applied to work on lower limb strength in extension, with the application of BFR, with two 30-minute sessions per week for four weeks. The exercise protocol, based on previous studies in older adults, will consist of three exercises: climbing on a step, knee extension from a seated position and sitting down and getting up from a chair.

干预措施: Blood flow restriction training (Other)

结局指标

主要结局

Change from baseline muscle power after treatment and at four weeks

时间窗: Screening visit, within the first seven days after treatment and four weeks follow-up visit

Muscle power will be assessed with the Sit To Stand 5 times. This tool consists of getting up and sitting down from a chair five times. This instrument has shown high reliability (CCI= 0.95). The unit of measurement is time in seconds, where the shorter the time the greater the muscle power

次要结局

  • Change from baseline muscle strength after treatment and at four weeks(Screening visit, within the first seven days after treatment and four weeks follow-up visit)
  • Change from baseline physical condition after treatment and at four weeks(Screening visit, within the first seven days after treatment and four weeks follow-up visit)
  • Change from baseline functionality after treatment and at four weeks(Screening visit, within the first seven days after treatment and four weeks follow-up visit)

研究者

发起方
Universidad Católica San Antonio de Murcia
申办方类型
Other
责任方
Principal Investigator
主要研究者

Rubén Cuesta-Barriuso, PhD

Principal Investigator

University of Oviedo

研究点 (1)

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