Effects of Photobiomodularion on Brain Connectivity and Cognitive Function in Cognitive Impairment

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age55+
SponsorUskudar University

About this trial

The goal of this clinical trial is to learn if transcranial photobiomodulation (t-PBM), a light-based brain therapy, can help improve memory and cognitive skills in older adults with amnestic mild cognitive impairment (aMCI). This condition involves memory problems that are greater than normal aging and may increase the chance of developing Alzheimer's disease.

The main questions this study aims to answer are:

1. Does t-PBM, when used together with cognitive training, improve memory and cognitive skills? 2. Does t-PBM change how certain brain areas communicate with each other, especially in the default mode network (DMN)?

Researchers will compare:

t-PBM plus cognitive training to sham (inactive) t-PBM plus the same cognitive training to see if the active light treatment leads to better cognitive improvement and healthier brain activity.

Participants will:

* Provide a blood sample so the research team can create a genetic profile; * Complete cognitive tests before and after the 4-week program; * Meet with a dietitian before and after the program so the research team can make sure diet stays consistent and does not influence brain results; * Have a brain fMRI scan before and after treatment to measure brain connectivity changes; * Take part in eight sessions of cognitive training; * Receive either active t-PBM or sham t-PBM during these sessions.

Eligibility criteria

Qualifiers

Age 55 years or older

Diagnosis of amnestic Mild Cognitive Impairment (aMCI)

Disqualifiers

Presence of a neurological disorder

Presence of a severe psychiatric disorder

Having a pacemaker or other implanted medical device that is not MRI-compatible

Trial design

Treatments tested in this trial

  • Active transcranial Photobiomodulation
  • sham transcranial Photobiomodulation
  • Cognitive Rehabilitation

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators