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临床试验/NCT05077046
NCT05077046已完成不适用

Efficacy of an Ergonomic Handwriting Pen - a Monocenter Randomized Controlled Counter-balanced Trial

University of Applied Sciences for Health Professions Upper Austria2 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2021年9月27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
17
试验地点
2
主要终点
Subjectively perceived muscle fatigue changes as determined with a Visual Analogue Scale (VAS)

研究概览

简要总结

This clinical investigation is a monocenter, prospective, randomized, controlled, counter-balanced, two-arm study investigating the effect of a novel ergonomic handwriting pen.

详细描述

Background:

Extended and prolonged handwriting activities can be exhausting for the writer and can lead to muscle cramps, irritations in the hand and lower arm as well as high pressures in the fingers and pain. As muscle pain in the upper extremities can affect hand writing quality, and as it is well known that high tendon activities and tissue pressures can lead to health issues, there is a need for ergonomic handwriting materials, especially for people with prolonged and extended handwriting activities (e.g. students).

Despite the high number of ergonomic handwriting pens on the market, clinical or scientific investigations for such pens are very rare. Indeed only a few studies on such pens are available, and there is little knowledge on how ergonomics can impact physiological and performance parameters. As high forces and pressures in the hand region over a long period of time can lead to health issues, a pen design targeting the reduction of grip forces and pressures was developed.

To investigate if this pen design can affect handwriting performance, perceived fatigue, pen and discomfort, the AWP pen study was developed. To follow international recommendations and to reduce potential bias as well as interpersonal variation, this study was designed as randomized controlled counter-balanced trial. The insights of this study can further help to develop novel handwriting tools and to support people with handwriting disabilities (e.g. stroke patients).

Methods:

研究设计

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

盲法说明

Participants will be informed that the effect of the handwriting pen design on different physiological parameters will be investigated within the study. Although participants know that they will execute the test battery twice with two different handwriting pens, they will receive no information on which of the pens will be the intervention of interest (intervention pen). To realize an efficient masking process, control pens will be exclusively created for the study. Control pens will be made of the same material and will contain cartridge. They will only differ in design.

入排标准

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

入选标准

  • Informed consent
  • People aged between 18 and 50 years
  • People free of acute or chronical diseases limiting their handwriting capabilities (e.g. Parkinson, hand/arm amputee)
  • Education level: at least high school diploma
  • People using a handwriting pen > once per week
  • Sufficient German language skills (min. B2 level - Questionnaire language)

排除标准

  • People with mental disorders limiting their writing performance
  • People with chronical fatigue syndrome
  • People incapable of concentrating on tasks for more than 30 minutes
  • Non-corrected visual disturbances

结局指标

主要结局

Subjectively perceived muscle fatigue changes as determined with a Visual Analogue Scale (VAS)

时间窗: 1 experimental day

Subjects will rate their subjectively perceived muscle fatigue prior and after the test battery by means of a Visual Analogue Scale (VAS). The VAS used for this study ranges from 0 (none) to 100 (strongly pronounced) points. Question: How would you describe your current muscle fatigue in your writing hand?

Subjectively perceived discomfort as determined with a Visual Analogue Scale (VAS)

时间窗: 1 experimental day

Subjects will rate their subjectively perceived discomfort in the writing hand prior and after the test battery by means of a Visual Analogue Scale (VAS). The VAS used for this study ranges from 0 (none) to 100 (strongly pronounced) points. Question: How would you describe your current discomfort in the writing hand?

次要结局

  • Handwriting speed as determined with a maze task (accuracy based)(1 experimental day)
  • Muscle pain estimated as determined with a Visual Analogue Scale (VAS)(1 experimental day)
  • Handwriting speed as determined with a dot in cycle task(1 experimental day)
  • Positioning accuracy as determined with a maze task (accuracy based)(1 experimental day)
  • Positioning accuracy as determined with a maze task (speed and accuracy based)(1 experimental day)
  • Handwriting speed as determined with a maze task (speed and accuracy based)(1 experimental day)
  • Handwriting speed as determined with a fatigue task(1 experimental day)
  • Handwriting performance as determined with the Handwriting Assessment Battery for Adults (HAB)(1 experimental day)
  • Usability as determined with a non-standardized questionaire(1 experimental day)

研究者

发起方
University of Applied Sciences for Health Professions Upper Austria
申办方类型
Other
责任方
Sponsor

研究点 (2)

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