跳至主要内容
临床试验/NCT04804501
NCT04804501Unknown不适用

Effect of Blue Light Glasses on Screen Usage After a Concussion in College Students

Rochester Institute of Technology1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2021年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
64
试验地点
1
主要终点
Time on Screen

研究概览

简要总结

Premature cessation of screen usage is a common behavior post-concussion, given the taxing nature of a screen-time task. In the academic setting, screen-time is a near unavoidable component, however, complete avoidance of class and screen use may in fact provoke psychological symptoms of anxiety and depression in students, for fear of falling behind in their studies. Thus, compensatory measures should be investigated to assist students as they attempt to maintain academic involvement throughout their concussion recovery. Blue light blocking glasses have been shown to significantly increase screen-time usage in individuals with post-concussion syndrome, yet these results are only representative of a small portion of the concussion population. Thus, we propose investigating whether blue light blocking glasses can prolong screen usage prior to symptom exacerbation, specifically in concussed students that are still within the normal recovery timeframe. This cross-sectional randomized clinical trial will provide further evidence of the utility blue light blocking glasses can offer as a therapeutic tool for students recovering from concussion. We would like to test volunteers from the Rochester Institute of Technology who have been treated by a medical provider within the university's health center. Blue light glasses will be worn during a one-time computer reading task while the subject is participating in the study. The total time for the complete the reading task is dependent upon the participant's symptom fluctuations; however, we suspect completion criteria will be met within 20 minutes from beginning. The risks in this study are minimal and results may increase our understanding of therapeutic tools for patients with ocular-driven concussion symptoms.

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
None

入排标准

年龄范围
18 Years 至 26 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Full-time student at RIT
  • •Diagnosed mild traumatic brain injury
  • •Between 18-26 years of age
  • •Within 3-14 days post-injury

排除标准

  • •Any head, neck, or face injury in the 1 year prior to the study (e.g., concussion, eye injury) other than the current injury
  • •History of vestibular or ocular dysfunction\
  • •Any neurological disorders (e.g., seizure disorders, closed head injuries with loss of consciousness greater than 15 minutes, CNS neoplasm, history of stroke)
  • •Injury more severe than mild traumatic brain injury (skull fracture, positive CT or MRI)
  • •Having taken pain medication within 8 hours prior to testing
  • •Not able to personally consent
  • •Deaf or hard of hearing.

研究组 & 干预措施

Blue Light Glasses (experimental)

Experimental

These subjects will wear the device (glasses) while performing a reading task.

干预措施: Blue Light Glasses (Device)

Blue Light Glasses (experimental)

Experimental

These subjects will wear the device (glasses) while performing a reading task.

干预措施: Computer Reading Task (Other)

No Glasses (control)

Other

These subjects will not wear the device (glasses) while performing a reading task.

干预措施: Computer Reading Task (Other)

结局指标

主要结局

Time on Screen

时间窗: 30 minutes or less

The amount of time a participant can spend on time, prior to meeting termination criteria, will be recorded and compared between experimental and control groups.

次要结局

未报告次要终点

研究者

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

Zachary Bevilacqua

Principal Investigator

Rochester Institute of Technology

研究点 (1)

Loading locations...

相似试验