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临床试验/NCT06353438
NCT06353438Unknown不适用

Implementation of a Community Based Exercise Program for Older Adults Using Hydraulic Resistance Equipment

College of Staten Island, the City University of New York2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2024年5月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
20
试验地点
2
主要终点
Timed Up and Go

研究概览

简要总结

The goal of this quasi-experimental study using a pre and post test design is to learn about the effect of participating in an exercise program with hydraulic exercise equipment on fall risk in the older adult population. The main questions it aims to answer are:

  • Does the use of hydraulic exercise equipment decrease fall risk in older adults?
  • Does the use of hydraulic exercise equipment improve function in older adults?

Participants will be evaluated pre and post intervention for strength, fall risk using Berg Balance Scale, Tinetti Balance and Gait Assessment, Timed Up and Go, and functional ability using the Lower Extremity Functional Scale. Participants will engage in an exercise program using 5 different pieces of hydraulic exercise equipment (Frei FACTUM® novus II line) 2x/week for for 6 weeks for 30-45 minutes each session. The equipment uses concentric movements only and works agonist and antagonist muscles with each machine (IE: push and pull, both concentric).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • Healthy adults

排除标准

  • Neurological condition
  • Surgery within last 6 months
  • Current injury
  • Inability to follow directions
  • Inability to participate in physical activity for any medical reason

结局指标

主要结局

Timed Up and Go

时间窗: 1 week prior to 1 week prior to intervention start date (pre-test) and 1 week post intervention end date (post-test) start date and 1 week post intervention end date

Objective functional outcome measure that assesses fall risk. Participants will start seated in a chair. When the assessor says "Go" the participant will stand up from the chair, walk 3 meters or 10 feet, turn around and walk back to the chair and sit down. The assessor will use a stopwatch to measure how much time it takes to complete this task. A score of 12 seconds or more indicates increased fall risk.

Lower Extremity Functional Scale

时间窗: 1 week prior to intervention start date (pre-test) and 1 week post intervention end date (post-test)

Objective functional outcome measure that determines functional ability during lower extremity tasks. Subjects rate their ability to perform 20 different lower extremity tasks on a 0-4 scale (0 is unable to complete activity and 4 is no difficulty). Scores range from 0-80. A total score of 80 means no difficulty with any task listed. 0 means unable to perform any task listed. The minimum clinically important difference (MCID) for the Lower Extremity Functional Scale is 9 points.

Berg Balance Scale

时间窗: 1 week prior to intervention start date (pre-test) and 1 week post intervention end date (post-test)

Objective functional outcome measure that assesses fall risk. Participants will move through 14 different tasks and will be assessed on their performance on a 0-4 scale. The higher the number given for a task, the better the participant's balance. The highest possible score is 56, which indicates low fall risk. The lower the score, the higher the fall risk. Minimal detectable change ranges from 5-7 depending on the diagnosis of the patient.

Tinetti Balance and Gait Assessment Tool

时间窗: 1 week prior to intervention start date (pre-test) and 1 week post intervention end date (post-test)

Objective functional outcome measure that assesses fall risk. This test looks at 9 different balance tasks (sitting balance, sit to stand, standing balance, for example) and 7 domains during gait (hesitancy to begin walking, step length and height, step symmetry, step continuity, for example). Balance score is out of 16 and gait score is out of 12. Total score is out of 28. The lower the score, the higher the fall risk.

次要结局

  • Strength(1 week prior to intervention start date and 1 week post intervention end date)

研究者

发起方
College of Staten Island, the City University of New York
申办方类型
Other
责任方
Sponsor

研究点 (2)

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