Light Therapy for Parkinson's Disease
What You Need to Know Before You Apply
What is the purpose of this trial?
The study looks to investigate the effects that light therapy delivered to the frontal cortex could have on Parkinson's disease related symptoms ( both cognitive and motor). The therapy is a non invasive technique that deliverers low level wavelength light to the front part of the head for 12 minutes. for this study the therapy will be done 3 times a week for 6 weeks. To measure the potential effects on the therapy in Parkinson symptoms, we will do a set of cognitive and motor test before and after the intervention to measure any changes as well as control for any potential markers such as age, sex, disease level, medication and exercise.
Do I need to stop taking my current medications for the trial?
Yes, you will need to stop taking your Parkinson's disease medication for certain assessments in the trial.
Is light therapy safe for humans?
How does light therapy differ from other treatments for Parkinson's disease?
Light therapy is unique because it is a non-drug treatment that uses light exposure to improve both motor and non-motor symptoms of Parkinson's disease, such as depression and sleep disturbances. Unlike traditional treatments that focus on replacing dopamine, light therapy may work by influencing the circadian system and has fewer side effects.12346
What data supports the effectiveness of the treatment Light Therapy for Parkinson's Disease?
Research shows that Light Therapy can significantly improve both movement and non-movement symptoms in Parkinson's patients, such as better motor function, reduced depression, and improved sleep. Studies also suggest that Light Therapy may help slow the progression of the disease when used alongside traditional treatments.12456
Are You a Good Fit for This Trial?
This trial is for individuals diagnosed with Parkinson's disease who can walk unassisted and consent to participate. It excludes those with recent head injuries, non-primary or atypical parkinsonism, deep brain stimulation devices, psychiatric disorders, cancer history, photosensitivity, or other movement/neurological conditions.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Pre-intervention Assessment
Cognitive and motor tests are conducted to establish baseline measures before the intervention
Treatment
Participants receive light therapy 3 times a week for 6 weeks
Post-intervention Assessment
Cognitive and motor tests are conducted to measure changes after the intervention
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Light Therapy
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Delaware
Lead Sponsor
NeuroThera
Industry Sponsor