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New treatment option for Mild Traumatic Brain Injury
Official title Pilot Study of Neurofeedback for Photosensitivity in Mild Traumatic Brain Injury
ClinicalTrials.gov ID: NCT06109909
What this study is testing
- What it's testing
- The goal of this study is to complete a pilot study testing the feasibility and acceptability of low-intensity pulse-based transcranial stimulation (LIP-tES) neurofeedback intervention for reducing photosensitivity symptoms in Veterans with a history of mild traumatic brain injury (mTBI). The study will also complete resting-state MRI scans to assess neurophysiological markers of photosensitivity and changes associated with LIP-tES intervention.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 65
You may be able to join if
- Ages 18-65
- Documented history of mTBI at least 6 months prior to initial study visit
- Documented symptoms of photosensitivity
- Eye exam within the last 12 months documenting best-corrected acuity of 20/20 or better, normal pupillary function, color vision, no abnormalities on...
You likely can't join if
- History of strabismus or amblyopia
- Significant ocular media opacity that could reduce the amount of light entering the pupil in one or both eyes
- Previous or current history of retinal or optic nerve pathology in one or both eyes
- History of stroke and/or visual neglect
- History of neurodegenerative disease (e.g., Parkinson's, multiple sclerosis)
- History of epilepsy or seizures
See the full eligibility criteria
- Ages 18-65
- Documented history of mTBI at least 6 months prior to initial study visit
- Documented symptoms of photosensitivity
- Eye exam within the last 12 months documenting best-corrected acuity of 20/20 or better, normal pupillary function, color vision, no abnormalities on OCT scan, and normal Humphrey Visual Field test
- History of strabismus or amblyopia
- Significant ocular media opacity that could reduce the amount of light entering the pupil in one or both eyes
- Previous or current history of retinal or optic nerve pathology in one or both eyes
- History of stroke and/or visual neglect
- History of neurodegenerative disease (e.g., Parkinson's, multiple sclerosis)
- History of epilepsy or seizures
- History of motor tics
- Current use of medications or substances that may severely affect pupillary response and/or increase photosensitivity
- Individuals with impaired decision-making capacity
- Illiterate or no English language proficiency
The study team makes the final eligibility decision.
Where it's taking place
- Boston, Massachusetts, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 65 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Boston, Massachusetts, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.