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Testing of a New Computer Screen for Patients With Persistent Concussion Symptoms (PCS).

Evaluation of a New Computer Screen for Patients With Persisting Concussion Symptoms Including Computer Screen Intolerance.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05660057
Enrollment
100
Registered
2022-12-21
Start date
2022-11-07
Completion date
2024-07-31
Last updated
2023-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-Concussion Symptoms

Brief summary

This study will examine whether a newly designed monitor for computers is better tolerated by concussed patients than the standard computer monitor. The information gathered from this study will contribute to the understanding of the persisting concussion symptoms including computer screen intolerance and photosensitivity, with the aim of helping those with concussions.

Detailed description

The study will involve completing a reading task on the standard computer monitor and the newly designed computer monitor. First, participants will be asked to rate their pre-test symptoms using a SCAT-III symptom checklist. Then they will read a short story and watch moving images on one of the devices (standard computer monitor or the newly designed computer monitor) for 30 minutes or until persisting concussion symptoms of moderate severity arise. Then, they will be asked to rate their post-test clinical symptoms using a SCAT-III symptom checklist. On a second visit, 7 to 10 days later, they will do the same activity on the other device. Each visit will take 60 minutes. The study will involve 100 patients with a history of concussion and computer screen intolerance.

Interventions

DEVICENew computer monitor

The device to be studied is a newly designed computer monitor and will be compared with the standard computer monitor.

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

Participants will read a short story and watch moving images for 30 minutes or until any of their persisting concussion symptoms will arise on the standard computer monitor and the newly designed computer monitor in two visits.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of persisting concussion symptoms (1 month to 5 year since concussion) * Must speak English * Must provide written consent * No alcohol/recreational drug use within 24 hours of intervention * No other neurological, psychiatric or ocular conditions

Exclusion criteria

* No diagnosis of Persisting Concussion Symptoms * Under the age of 18, over the age of 65 * Other neurological/psychiatric or ocular conditions * Alcohol or recreational drug use within 24 hours of intervention

Design outcomes

Primary

MeasureTime frameDescription
The investigators believe that patients will subjectively perceive the new monitor to be a more effective reading device than the standard monitor.Two visits 7 to 10 days apartSCAT-III Symptoms checklist will be completed before and after study tasks (reading an excerpt and watching a moving image) to measure symptoms number and severity arising after the study task on a standard monitor and compare it to the newly designed monitor.

Countries

Canada

Contacts

Primary ContactMozhgan Khodadadi, MA
mozhgan.khodadadi@uhn.ca416-603-5800

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026