Purpose

We will be looking at 3 treatment arms in the form of different type of glasses to see if one is superior to helping kids have sustained a concussion and are symptomatic.

Conditions

Eligibility

Eligible Ages
Between 9 Years and 17 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Sustained a concussion > 6 weeks < 16 weeks from date of initial visit - Criteria for concussion: formally diagnosed by physician - Minimum best corrected visual acuity: 20/25 in right and left eyes at distance and 20/30 both eyes at near - Minimum Stereopsis: 500" global - CISS score > 16 - Refractive error at least + 0.50D sphere or cylinder - Ability to clear > 0.50 cycles per minute in monocular accommodative flipper of and binocular accommodative flipper of +/-1.50

Exclusion Criteria

  • Diplopia from nerve palsies - Retinal pathology - Previous treatment of any amount of bifocal lenses and base in prism since concussion. - Vision therapy > 6 weeks since concussion

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Investigator)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Single vision glasses
Typical glasses prescribed for children to correct only distance refractive error and to be worn all waking hours.
  • Device: Glasses
    Glasses traditionally prescribed for refractive error
Experimental
Single vision glasses with anti-glare coating
Typical glasses prescribed for children to correct only distance prescription with anti-glare coating and to be worn all waking hours.
  • Device: Glasses
    Glasses traditionally prescribed for refractive error
Experimental
Eyezen
Commercially available, low-powered, progressive addition lenses glasses with anti-glare coating to be worn all waking hours
  • Device: Glasses
    Glasses traditionally prescribed for refractive error

More Details

Status
Terminated
Sponsor
University of Alabama at Birmingham

Study Contact

Detailed Description

Recent studies have shown children who sustain a concussion are susceptible to having chronic symptoms (post-concussion syndrome). This chronicity can lead to delays in returning to learn and returning to play. Blurry vision, double vision, eye strain and eye tracking problems are some of the reported chronic symptoms that can affect patients' daily activities. Concussion awareness has increased recently and there is a surge of interest to better understand and treat the symptoms of post-concussion syndrome. Currently, ocular treatment for patients are often empirically determined. Common treatments are vision therapy and/or bifocal glasses. There has yet to be any standardization or prospective studies looking into treatment for these concussed patients with ocular symptoms and findings. The objective of this protocol is to compare three different types of glasses (typical prescription glasses for kids, typical glasses for kids with anti-glare coating, and progressive addition lenses with anti-glare coating) as treatment options for participants who are still symptomatic four weeks out from their concussion. The main outcome is the effectiveness of these three different options in reducing patients' symptoms and improving the participants' visual findings.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.