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临床试验/NCT04920201
NCT04920201已完成不适用

The Effect of Exercise With Wearable Walking Assist Robot in Various Environments in Healthy Adults

Samsung Medical Center2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年6月7日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
2
主要终点
Change from baseline performance on gait speed after the intervention

研究概览

简要总结

This single-blinded, randomized, controlled trial includes 60 healthy adults. The participants were randomized to four different groups. The first group performed over-ground walking without GEMS-H, the second group performed over-ground walking with GEMS-H applied resistance mode, the third group performed stair ascent with GEMS-H applied assist mode, and the fourth group were designated as the group that performed inclined gait with GEMS-H applied assist mode on a treadmill. Each group is divided in 15 participants.

详细描述

At the first visit, the subjects are fully informed of the study if appropriate after determining whether they meet the selection criteria. If the subjects meet the selection criteria, the participants were randomized to four different groups. The first group performed over-ground walking without GEMS-H, the second group performed over-ground walking with GEMS-H with resistance mode, the third group performed stair ascent with GEMS-H with assist mode, and the fourth group were designated as the group that performed inclined gait with GEMS-H with assist mode on a treadmill. Each group is divided in 15 participants. Each group completed 30 minutes exercise at least three times per week (total 10 sessions). All measurements were conducted before and after the intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Investigator)

盲法说明

Single masking (Outcomes Assessor)

入排标准

年龄范围
65 Years 至 84 Years(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy adults aged 50 to less than 85 years without a history of central nervous system disease

排除标准

  • Those who have difficulty walking independently due to problems such as visual field defects or fractures
  • Those with severe arthritis or orthopedic problems limiting passive range of motion (ROM) of the lower extremities (knee flexion contracture >10°, knee flexion ROM <90°, hip flexion contracture >25°, ankle plantar flexion contracture >15°)
  • Those who have difficulty understanding the exercise program due to severe cognitive decline (Korean-Mini-Mental State Examination, K-MMSE≤10)
  • Those who have difficulty participating in exercise programs due to adult diseases such as uncontrolled hypertension and diabetes
  • Those who are at risk of falling while walking due to severe dizziness
  • Those who are less than 140 cm or more than 185 cm in height that is not suitable size for the wearing of the walking assistance robot
  • Those who are overweight based on body mass index (BMI) 35 or higher

结局指标

主要结局

Change from baseline performance on gait speed after the intervention

时间窗: Baseline, After the intervention(day12)

Measure of self selected speeds by measuring the time it takes an individual to walk 10 meters. To perform the test, patient walks 10 meters (33 ft) and the time is measured when the leading foot crosses the start line and the finish line. The instructions are: "Please walk this distance at your normal pace when I say go."

次要结局

  • Change from baseline performance on Short Physical Performance Battery (SPPB) after the intervention(Baseline, After the intervention(day12))
  • Change from baseline performance on muscle strength after the intervention(Baseline, After the intervention(day12))
  • Change from baseline performance on Timed Up and Go test (TUG) after the intervention(Baseline, After the intervention(day12))
  • Change from baseline performance on EuroQol 5 Dimensions (EQ-5D) after the intervention(Baseline, After the intervention(day12))
  • Change from baseline performance on Berg Balance Scale (BBS) after the intervention(Baseline, After the intervention(day12))
  • Change from baseline performance on Geriatric Depression Scale (GDS) after the intervention(Baseline, After the intervention(day12))
  • Change from baseline performance on metabolic energy expenditure after the intervention(Baseline, After the intervention(day12))
  • Change from baseline performance on Functional Reach Test (FRT) after the intervention(Baseline, After the intervention(day12))
  • Change from baseline performance on Four Square Step Test (FSST) after the intervention(Baseline, After the intervention(day12))
  • Change from baseline performance on Fall Efficacy Scale-Korea (FES-K) after the intervention(Baseline, After the intervention(day12))

研究者

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

Yun-Hee Kim

Dr., Ph.D.

Samsung Medical Center

研究点 (2)

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