Physiological Effect of Non-invasive Photobiomodulation on Cognition and Mood in Older Adults With Subjective Cognitive Impairment
1 other identifier
interventional
80
1 country
1
Brief Summary
Subjective cognitive impairment (SCI) is a non-clinical condition manifesting as a self-reported decline in cognitive function without objective clinical evidence, and is prevalent among older adults and strongly associated with declining mood. This study explores the potential of photobiomodulation (PBM) as a therapeutic intervention for SCI. PBM, using near-infrared light, is a non-invasive neuromodulation approach that has shown promise in improving neuronal function, blood flow, and reducing inflammation in both healthy adults and patients with neurological conditions, including dementia and depression. This study proposes investigating the potential of forehead (tPBM), intranasal (iPBM) and vagal (vPBM) PBM to enhance mood and cognitive function in individuals with SCI as a proof of concept for the future use of PBM as therapy for cognitive decline in general. This study will recruit approximately 80 participants with SCI for the study, and the total expected duration of the participant\'s participation in the study is 5 weeks. The active and sham Neuro 5T device consisting of a headset with a built-in controller, nasal and neck applicators will be used. The nasal and neck applicators each contains a single LED and will be placed into the nostril or neck and secured into place. The headset contains multiple LEDs in a wearable applicator and may be adjusted. The Neuro 5T also contains telemetry features to allow documentation of patient usage of the device. LEDs are semiconductor electronic components that emit light. Participants will be given PBM devices for in-home usage, 2 times a day, 7 days a week, for 5 weeks. Participants will undergo EEG, MRI, cognitive and nasal microbiome assessments before and after the 5-week period.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jun 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 14, 2025
CompletedFirst Posted
Study publicly available on registry
March 3, 2026
CompletedStudy Start
First participant enrolled
June 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2028
Study Completion
Last participant's last visit for all outcomes
July 1, 2028
March 3, 2026
October 1, 2025
2.1 years
July 14, 2025
February 25, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Geriatric Depression Scale (Short Form)
The Geriatric Depression Scale (Short Form), or GDS-SF, is a 15-item questionnaire used to screen older adults for depression. It is a simplified version of the original 30-item GDS, designed to be easier to administer, especially to those who are physically ill, easily fatigued, have short attention spans, or have mild cognitive impairment. A score of 5 or greater suggests the need for further evaluation for depression.
The first assessment will take place before participants receive treatment, and another session no more than 2 weeks after their final treatment session.
Montreal Cognitive Assessment
The Montreal Cognitive Assessment (MoCA) is a rapid screening instrument designed to detect mild cognitive impairment. It assesses various cognitive domains, including attention, memory, language, and executive functions. The MoCA is a brief test, taking approximately 10 minutes to administer, and is widely used in clinical and research settings.
The first assessment will take place before participants receive treatment, and another session no more than 2 weeks after their final treatment session.
Secondary Outcomes (4)
EEG signal metrics and spatial-temporal pattern
Two sessions, to be completed no more than 2 weeks before the start of the treatment sessions and then no more than 2 weeks after the conclusion of all treatment sessions
Alpha diversity
Two nasal swab samples collected; one before the administration of the first treatment session, and one after the last treatment session.
Resting-state fMRI
Two scans, to be completed no more than 2 weeks before the start of the first treatment session and no more than 2 weeks after the conclusion of the last treatment session.
Beta diversity
Two nasal swab samples collected; one before the administration of the first treatment session, and one after the last treatment session.
Study Arms (4)
Sham
SHAM COMPARATORParticipants will have the devices positioned but not turned on
tPBM (forehead PBM)
ACTIVE COMPARATORParticipants will have the devices positioned but only the tPBM device turned on
iPBM (intranasal PBM)
ACTIVE COMPARATORParticipants will have the devices positioned but only the iPBM device turned on
vPBM (vagus PBM)
ACTIVE COMPARATORParticipants will have the devices positioned but only the vPBM device turned on
Interventions
the application of red and near-infrared light
Eligibility Criteria
You may qualify if:
- Affirmative responses to two questions on a self-report questionnaire: "Do you feel your memory is becoming worse?" "If so, are you concerned?"
You may not qualify if:
- Presence of clinically diagnosed dementia, mild cognitive impairment, depression, post-traumatic stress disorder, obsessive-compulsive disorder, eating disorder(s), schizophrenia, or other psychiatric disorders.
- History of a manic, hypomanic, or mixed depressive episode.
- Treatment with electroconvulsive therapy, intravenous and/or intranasal ketamine in the 6-weeks prior to study enrolment.
- History of substance-use disorder in the past 12 months.
- Presence of current alcohol-use disorder.
- A positive urine toxicology screen for non-prescribed substance use.
- A positive pregnancy test at screening.
- A history of major medical or neurological illness.
- A history of traumatic brain injury, stroke, seizures, or previous brain surgery.
- Current use of anti-coagulants.
- Contraindications to magnetic resonance imaging (MRI) scanning.
- Being currently involved in other intervention studies.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Baycrestlead
Study Sites (1)
Rotman Research Institute
Toronto, Ontario, M6A 2E1, Canada
Related Publications (35)
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BACKGROUND
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, CARE PROVIDER
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Scientist
Study Record Dates
First Submitted
July 14, 2025
First Posted
March 3, 2026
Study Start (Estimated)
June 1, 2026
Primary Completion (Estimated)
July 1, 2028
Study Completion (Estimated)
July 1, 2028
Last Updated
March 3, 2026
Record last verified: 2025-10
Data Sharing
- IPD Sharing
- Will not share