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临床试验/NCT07049809
NCT07049809已完成不适用

Targeting Sarcopenia and Frailty: Multicomponent Exercise With Focal Muscle Vibration to Reduce Sarcopenia, Frailty Levels, and Cognitive Impairment in Institutionalized Older Adults

Universitat Internacional de Catalunya1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年7月2日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
1
主要终点
Short Physical Performance Battery

研究概览

简要总结

This study aimed to evaluate the efficacy of multicomponent exercises (aerobic exercises, strength exercises, and balance exercises), individualized with the application of a focal muscle vibration machine at the lower extremities, on parameters of sarcopenia (a muscle disease) in health-related physical fitness, physical performance, frailty levels, and cognitive function, falls, and hospitalizations in older adults.

Focal muscle vibration is a type of therapeutic technique used with the application of six capsules placed on the lower extremities, three on each bed, each of which generates a tolerable vibration depending on the stimulation of the muscles. It is neither painful nor counterproductive to the muscles in the lower extremities.

Multicomponent exercises refer to the application of exercises through three different modalities: aerobic exercises, strength exercises, and balance exercises. We alternate these three types of exercises to achieve millions of health benefits. The multi-component program will be individualized based on each individual's abilities to avoid risks and achieve maximum benefits.

详细描述

This study presents the hypothesis that it will allow researchers to significantly improve health parameters in very fragile people, which may have positive impacts at both the individual and community levels. The incorporation of focal vibration as part of a multicomponent approach to exercise is innovative and opens new lines of research in the field of rehabilitation and developmental health. Currently, I understand that there is a growing need to address the healthy development and fragility of the large adult population, given the increasing proportion in today's society and the reptes associated with the loss of functional abilities, which studies can allow other scientists to see the benefits of the program in different areas. health parameters after 3 months of intervention.

The participation in the study will include:

  • Authorizing the investigators to access your medical history. This will allow the investigators to collect information about the clinical data of the participants.
  • Authorizing the investigators to share coded clinical information with other research teams. Theparticipant authorize access to information related to hospitalizations and drugs consumed.
  • Allow the collection of data both at the beginning and after the intervention after 3 months by the external research team. Different data will be collected in a single day both at the beginning and at the end of the intervention, with an approximate duration of 35/40 minutes per person. The data that will be collected will give the researchers information about functional status, muscle strength and power and cognitive level. In addition. the levels of sarcopenia in dominant leg will be evaluated with ultrasound. The ultrasound assessment is a painless test through which an attempt will be made to see the amount of muscle and fat present at the level of the dominant lower extremity. In addition, at the beginning and end of the intervention a blood test will be performed by CST personnel. This analysis will be used to evaluate different blood markers of the participants and see how they respond to the different intervention programs.
  • Randomization to one of the 2 study groups: a focal vibration group with multicomponent exercise, an exercise only group.

Prior to the start of the intervention program, and after this 3-month period, a series of functional tests, tests, muscle ultrasound and a blood analysis will be performed. These tests are tests that are normally used in clinics or hospitals as functional or force assessments in the geriatric population. Once the initial evaluation and data analysis has been carried out, a group will subsequently be randomly assigned to one of the 3 groups that is proposed by the study. If still assigned to group 1) combined exercise with focal vibration, repeat for 3 months, 3 days per week and 30 minutes per day, multicomponent exercises (strength, aerobic exercise and balance) combined with focal muscular vibration. In case it continued to be assigned to group 2) multicomponent exercise, repeat for 3 months, 3 days per week and 30 minutes a day, multicomponent exercises (strength, aerobic exercise and balance).

研究设计

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

入排标准

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

入选标准

  • •people over 75 years of age,
  • •score ≥18 on the Mini-Mental State Exam (MMSE)
  • •score on the Clinical Frailty Scale between 1-6
  • •be institutionalized
  • •ability to sit unassisted on a chair or in a wheelchair

排除标准

  • •progressive degenerative diseases
  • •uncontrolled symptomatic cardiovascular or respiratory disease
  • •current cancer under treatment
  • •severe audiovisual impairment

研究组 & 干预措施

Combination Intervention group

Experimental

2-month intervention. 3 days/week. 30 minutes/day. Will receive a multicomponent program based on aerobic training, resistance training and balance training, combined with focal muscle vibration. Of the 3 days of weekly intervention, 1 day will be aerobic exercise combined with focal muscle vibration, 1 day resistance exercise with focal muscle vibration and 1 day of balance exercise with focal muscle vibration.

The combined program will be individualized based in the intrinsic capabilities of each individual.

干预措施: Focal Muscle Vibration (Combination Product)

Combination Intervention group

Experimental

2-month intervention. 3 days/week. 30 minutes/day. Will receive a multicomponent program based on aerobic training, resistance training and balance training, combined with focal muscle vibration. Of the 3 days of weekly intervention, 1 day will be aerobic exercise combined with focal muscle vibration, 1 day resistance exercise with focal muscle vibration and 1 day of balance exercise with focal muscle vibration.

The combined program will be individualized based in the intrinsic capabilities of each individual.

干预措施: Multicomponent Exercise (Other)

Multicomponent Exercise Group

Active Comparator

3-month intervention. 3 days/week. 30 minutes/day. Will receive a multicomponent program based on aerobic training, resistance training and balance training.

The combined program will be individualized based in the intrinsic capabilities of each individual.

干预措施: Multicomponent Exercise (Other)

结局指标

主要结局

Short Physical Performance Battery

时间窗: From enrollment to the end of treatment at 12 weeks

Short Physical Performance Battery (SPPB) is a standardized test that evaluates Balance, Gait speed and Lower limb strength (via chair stands). Has a total puntuaction of 12 points: 0-3: Severe physical limitation, 4-6: Moderate limitation, 7-9: Mild limitation, 10-12: Good physical function. The SPPB (Short Physical Performance Battery) is closely related to sarcopenia because it assesses physical function, which is one of the key diagnostic criteria for sarcopenia.

次要结局

  • Demographic and anthropometric assessments(from enrollment to 12 weeks after treatment)
  • Handgrip(from enrollment to 12 weeks after intervention)
  • SARC-F(from enrollment to 12 weeks after intervention.)
  • Clinical Frailty Scale(from enrollment to 12 weeks after intervention)
  • Muscle ultrasound(from enrollment to 12 weeks after intervention.)
  • Mini Mental State Exam(from enrollment to 12 weeks after intervention.)
  • Demographic and anthropometric assessments(from enrollment to 12 weeks after treatment)
  • Handgrip(from enrollment to 12 weeks after intervention)
  • SARC-F(from enrollment to 12 weeks after intervention.)
  • Clinical Frailty Scale(from enrollment to 12 weeks after intervention)
  • Muscle ultrasound(from enrollment to 12 weeks after intervention.)
  • Mini Mental State Exam(from enrollment to 12 weeks after intervention.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sergi Rodriguez Rodriguez

Physiotherapist. Professor at the department of Medicine.

Universitat Internacional de Catalunya

研究点 (1)

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