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Groningen Meander Walking Test in Older Adults With Balance Problems (GMWT-OA)

2026年9月11日 更新者:Elif AYGUN POLAT、Ordu University

Test-Retest Reliability and Construct Validity of the Groningen Meander Walking Test in Older Adults With Self-Reported Balance Problems and/or a History of Falls

This observational cross-sectional psychometric study aims to examine the test-retest reliability and construct validity of the Groningen Meander Walking Test in older adults with self-reported balance problems and/or a history of falls. Participants aged 65 years or older will be recruited from the Orthopedics and Traumatology outpatient clinic of Ordu University Training and Research Hospital. The Groningen Meander Walking Test will be performed twice during the first session and repeated in a second session to assess within-day and between-day reliability. Construct validity will be evaluated using the Timed Up and Go Test, Figure-of-Eight Walking Test, Berg Balance Scale, and Falls Efficacy Scale-International. The study will also explore the ability of the Groningen Meander Walking Test to discriminate between participants with low and increased fall risk according to the Berg Balance Scale.

研究概览

地位

完全的

详细说明

This observational cross-sectional study will evaluate the reliability and validity of the Groningen Meander Walking Test in older adults with self-reported balance problems and/or a history of falls. Participants aged 65 years or older will be recruited from the Orthopedics and Traumatology outpatient clinic of Ordu University Training and Research Hospital.

The Groningen Meander Walking Test will be administered in two assessment sessions to examine within-day and between-day test-retest reliability. Completion time and overstep score will be recorded. Construct validity will be assessed by comparing Groningen Meander Walking Test outcomes with established clinical measures of functional mobility, curved walking performance, balance, and concern about falling.

The study aims to determine whether the Groningen Meander Walking Test is a clinically useful assessment tool for advanced walking ability in older adults with balance problems and/or fall history.

研究类型

观察性的

注册 (实际的)

71

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 年长者

接受健康志愿者

不

取样方法

非概率样本

研究人群

Adults aged 65 years or older with self-reported balance problems and/or a history of falls within the previous 12 months will be recruited from the Orthopedics and Traumatology outpatient clinic of Ordu University Training and Research Hospital. Eligible participants will be individuals who can walk independently with or without a single walking aid and who are able to complete the clinical walking and balance assessments.

描述

Inclusion Criteria:

Aged 65 years or older Self-reported balance problems during activities of daily living and/or a history of at least one fall within the previous 12 months Able to walk independently with or without a single walking aid Able to understand and follow verbal instructions Willing to provide written informed consent

Exclusion Criteria:

Presence of neurological, vestibular, visual, orthopedic, systemic, or medical conditions that may substantially affect gait or balance Acute lower-extremity injury or recent lower-extremity surgery Severe pain preventing completion of the walking or balance tests Cognitive impairment that may limit the ability to understand or follow test instructions Inability to walk independently without personal assistance Use of a rollator

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
Older Adults With Balance Problems
Participants aged 65 years or older with self-reported balance problems and/or a history of falls within the previous 12 months will undergo clinical assessments, including the Groningen Meander Walking Test, Timed Up and Go Test, Figure-of-Eight Walking Test, Berg Balance Scale, and Falls Efficacy Scale-International. No intervention will be administered.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Groningen Meander Walking Test Completion Time
大体时间:Baseline and 3 to 7 days after baseline
Completion time of the Groningen Meander Walking Test will be recorded in seconds. The mean of the start-to-end and end-to-start completion times will be used as the Groningen Meander Walking Test completion time. A longer completion time indicates poorer advanced walking performance.
Baseline and 3 to 7 days after baseline

次要结果测量

结果测量
措施说明
大体时间
Groningen Meander Walking Test Overstep Score
大体时间:Baseline and 3 to 7 days after baseline
The number of times the participant's foot completely lands outside the marked pathway will be recorded. Oversteps from the start-to-end and end-to-start directions will be summed. A higher score indicates poorer stepping accuracy.
Baseline and 3 to 7 days after baseline
Timed Up and Go Test Completion Time
大体时间:Baseline
Functional mobility will be assessed using the Timed Up and Go Test. The time required to stand from a chair, walk 3 meters, turn, return to the chair, and sit down will be recorded in seconds. A longer time indicates poorer functional mobility.
Baseline
Figure-of-Eight Walking Test Completion Time
大体时间:Baseline
Curved walking performance will be assessed using the Figure-of-Eight Walking Test. Completion time will be recorded in seconds, and a longer time indicates poorer advanced walking performance.
Baseline
Berg Balance Scale Score
大体时间:Baseline
Functional balance will be assessed using the Berg Balance Scale. Total scores range from 0 to 56, with higher scores indicating better balance performance and lower fall risk.
Baseline
Falls Efficacy Scale-International Score
大体时间:Baseline
Concern about falling during daily activities will be assessed using the Falls Efficacy Scale-International. Total scores range from 16 to 64, with higher scores indicating greater concern about falling.
Baseline

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:ELİF A POLAT, Assoc.Prof.、Ordu university

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年7月15日

初级完成 (实际的)

2026年8月30日

研究完成 (实际的)

2026年9月7日

研究注册日期

首次提交

2026年7月3日

首先提交符合 QC 标准的

2026年7月3日

首次发布 (实际的)

2026年7月9日

研究记录更新

最后更新发布 (实际的)

2026年9月15日

上次提交的符合 QC 标准的更新

2026年9月11日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • ODU-SBFTR-AYGUNPOLAT-007

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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