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临床试验/NCT04700605
NCT04700605Unknown不适用

Intra-rater Reliability and Agreement Between Static Balance Test Using Nintendo Wii Balance Board and Gait Test Under Dual Task Conditions in Community-dwelling Older Adults.

Aalborg University Hospital1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2020年10月27日最近更新:
适应症

试验速览

阶段
不适用
入组人数
30
试验地点
1
主要终点
Intra-rater reliability for the gait test and the WBB test.

研究概览

简要总结

Agreement and intra-rater reliability between static balance test using Nintendo Wii Balance Board and gait test under dual-task conditions in community-dwelling older adults.

详细描述

Participants:

Investigators aim to recruit a minimum of 30 participants aged 65 years or above through convenience sampling at an senior activity centre in the Municipality of Aalborg. Participants inclusion critiria is age about 65, the ability to stand for 30 seconds unaided and the ability to walk 8 meters. Exclusion critiria is severe cognitive impairment (e.g., dementia).

Procedure:

Each participant will undergo two testdays separated by approximately two weeks. Both testdays have the same number and order of tests and are placed approximately the same time of the day. At the first testday descriptive information for each participant is collected.

Measuring device:

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

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

入选标准

  • Minimum 65 years old.
  • Community dwelling

排除标准

  • Unable to stand unsupported for 30 seconds
  • Unable to walk 8 meters unsupported

结局指标

主要结局

Intra-rater reliability for the gait test and the WBB test.

时间窗: Through study completion, app. 8 months.

Comparing the dual task costs for each test between test and retest. Assessments through intraclass correlation coefficient and reportings in accordance with Guidelines for Reporting Reliability and Agreement Studies (GRRAS).

次要结局

  • Agreement between the gait test and the WBB test as dual task measurements.(Through study completion, app. 8 months.)
  • Descriptive data.(Through study completion, app. 8 months.)

研究者

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

Martin Eriksen

Medical student

Aalborg University Hospital

研究点 (1)

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