Depression Research Study
Researchers at the Nathan Kline Institute and NYU Langone Health are conducting a research study to learn how near-infrared light energy may affect blood flow and mood in people experiencing depression.
Fast Facts
Experiencing Symptoms of Depression
Ages 18-65
Compensation Provided
Conducted in
New York
Study Background
Researchers at the Nathan Kline Institute and NYU Langone Health are studying whether near-infrared light therapy can potentially improve symptoms of depression.
We want to determine if applying near-infrared light energy to the forehead changes blood flow in the brain, and whether or not it can affect mood. Near-infrared energy is like light but is not visible to the human eye.
This study will involve 20 appointments where participants will be asked to:
- Answer surveys
- Complete MRIs
- Undergo 16 treatment sessions where they may or may not be exposed to near-infrared energy
- Report any side effects that they might experience
Study Background
Researchers at the Nathan Kline Institute and NYU Langone Health are studying whether near-infrared light therapy can potentially improve symptoms of depression.
We want to determine if applying near infrared light energy to the forehead changes blood flow in the brain, and whether or not it can affect mood. Near-infrared energy is like light but is not visible to the human eye.
This study will involve 20 appointments where participants will be asked to:
Answer surveys
Complete MRIs
Undergo 16 treatment sessions where they may or may not be exposed to near-infrared energy
Report any side effects that they might experience
Additional Information
This research study is being done to determine whether near-infrared light therapy can potentially improve symptoms of depression.
You may qualify for this study if you meet the following criteria.
Inclusion Criteria:
- Ages 18-65
- Experiencing symptoms of depression
- No dependence on alcohol or other drugs
- No diagnosis of any neurological disorders (e.g., dementia, TBI, stroke, seizure disorder)
- No history of antisocial personality disorder
- If female, not currently pregnant
- No history of ECT in the last 12 months or lifetime history of Vagus Nerve Stimulation (VNS)
- No current significant skin conditions on the forehead
This study will last approximately 11-20 weeks and will involve about 20 appointments.
During these appointments participants will be asked to share information about their mental and physical health, complete 2 brain scans, undergo 16 treatment sessions where they may or may not be exposed to near-infrared energy, and report on any side effects. There will also be a follow-up appointment.
Participants will receive compensation for time and travel for completing all study visits. If they choose to withdraw before the study is completed, they will only be compensated for completed visits.
There is no cost for you to participate in our research study.
