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临床试验/NCT05317377
NCT05317377已完成不适用

Leap Motion Controller Based Exergame Therapy in Geriatric Individuals

Istanbul Medipol University Hospital2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2021年7月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
2
主要终点
Grip Strength Test

研究概览

简要总结

Little is Known about the effects of leap motion based exergame therapy on different functions of elderly adults. The purpose of this study was to evaluate the effect of leap motion based exergame therapy on hand function, cognitive function and quality of life in older adults

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 (Participant)

盲法说明

participants will be included in the study and randomly divided into two groups using block randomization in Microsoft Excel 'RAND(WS)' function.

入排标准

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

入选标准

  • 50 years old and over,
  • having adequate hand function,
  • ability to follow commands,
  • 24< points in MMSE

排除标准

  • presence of exercise contraindications
  • 14 or more points on the Geriatric Depression Scale
  • diagnosis of dementia
  • recent (acute) hand or arm injury

结局指标

主要结局

Grip Strength Test

时间窗: changes after 8 weeks

A hand dynamometer (pinch meter gauge; Jamar® Hand Dynamometer - Hydraulic - 200 lb Capacity. Patterson Medical Illinois, USA) will be used to determine the grip strength of the participants. While taking the measurements, the patients will be seated with the shoulder adducted and neutrally rotated, elbow flexed at 90°, forearm and wrist in neutral position. Each grip test will be repeated three times and the highest score for the affected extremity will be used for further analysis.

次要结局

  • Duruöz Hand Index(changes after 8 weeks)
  • Purdue Pegboard Test(changes after 8 weeks)
  • Pittsburgh Rehabilitation Participation Scale(changes after 8 weeks)
  • Digit Span Test(changes after 8 weeks)
  • Box and Block Test(changes after 8 weeks)
  • World Health Organization Quality of Life Instrument-Older Adults Module(changes after 8 weeks)
  • Stroop Test(changes after 8 weeks)

研究者

发起方
Istanbul Medipol University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Farzin Hajebrahimi, PhD

Principal Investigator

Istanbul Medipol University Hospital

研究点 (2)

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