The Effect of Varying Brightness on Palpebral Aperture
1 other identifier
interventional
40
1 country
1
Brief Summary
We aim to establish the point at which glare from bright lights begins to engage our eyelids - causing us to "squint". We will be using a video camera with an LED ring light around it facing the volunteer and we will record the eyelid position as the light brightness is increased gradually. Many studies have looked at the effect glare has on a person through qualitative questionnaires but few have been able to quantify this.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2022
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 14, 2022
CompletedStudy Start
First participant enrolled
January 14, 2022
CompletedFirst Posted
Study publicly available on registry
January 27, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 21, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
February 21, 2022
CompletedJanuary 27, 2022
January 1, 2022
1 month
January 14, 2022
January 14, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The point at which the eyelid begins to contract under what brightness level
Using a light meter, ring light, and EEG machine
All carried out within a 2 week period
Study Arms (1)
The observation of eyelid positioning and EEG pulses from the eyelid on increasing brightness
EXPERIMENTALIn a dimly lit room the participant will place their chin on the slit lamp We will use t he optimal background illumination used for Humphrey and Goldman visual fields which is 31.5 apostilbs (10Lux 9 They will look into the video camera placed 50cm away, which will have a dimmable remote control ring light fitted around it. The part icipant will have a reference measure taped to the headrest and three electrodes placed around the right eye. One active electrode place on the lower lid and one reference electrode towards the temporal margin and one earth electrode placed on the forehead The brightness of the ring light will be increased via the dimmer switch whilst simultaneously recording the lux with the LED light meter. The participant will be advised t o close their eyes if the brightness becomes uncomfortable and this will be repea ted three times.
Interventions
Up to 30 seconds, three times, looking into a video camera as glare is incrementally increased.
Eligibility Criteria
You may qualify if:
- Aged between 18 and 65 years of age
- A member of the Royal Free NHS trust
You may not qualify if:
- No known ocular pathology
- No lid problems/ptosis or previous lid surgery
- No contact lenses in for duration of experiment
- No pseudophakia
- No neurological disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Edinburghlead
- National Health Service, United Kingdomcollaborator
- Royal Free Hospital NHS Foundation Trustcollaborator
Study Sites (1)
Ophthalmology, Royal Free Hospital
London, NW3 2QY, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 14, 2022
First Posted
January 27, 2022
Study Start
January 14, 2022
Primary Completion
February 21, 2022
Study Completion
February 21, 2022
Last Updated
January 27, 2022
Record last verified: 2022-01