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临床试验/NCT05121272
NCT05121272已完成不适用

Fatigability and Cognitive Demand With Aging

University of Oklahoma1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年10月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
1
主要终点
force

研究概览

简要总结

This study will determine the influence of a cognitive task performed during fatiguing contractions.

详细描述

Individuals will participate in one familiarization session followed by 3 randomized experimental sessions (crossover design).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Other
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Healthy individuals aged between 18-35 and 65-90

排除标准

  • •Metal implants or joint replacement. neuromuscular disease

研究组 & 干预措施

young men

Experimental

Individuals will participate in 1 familiarization and 3 test sessions

干预措施: cognitive task (Behavioral)

young women

Experimental

Individuals will participate in 1 familiarization and 3 test sessions

干预措施: cognitive task (Behavioral)

older men

Experimental

Individuals will participate in 1 familiarization and 3 test sessions

干预措施: cognitive task (Behavioral)

older women

Experimental

Individuals will participate in 1 familiarization and 3 test sessions

干预措施: cognitive task (Behavioral)

结局指标

主要结局

force

时间窗: Each session will take approximately 2-3 hours (total of 4 test sessions)

Change in force of the arm muscles will be evaluated with a custom made device during each test session

fatigue

时间窗: Each session will take approximately 2-3 hours (total of 4 test sessions

changes in fatigue will be assessed with questionnaires

anxiety levels

时间窗: Each session will take approximately 2-3 hours (total of 4 test sessions

changes in anxiety levels quantified with a questionnaire

arterial pressure

时间窗: Each session will take approximately 2-3 hours (total of 4 test sessions

changes in arterial pressure will be quantified with a non-invasive device (finometer)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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