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Clinical Trials/NCT05408637
NCT05408637CompletedPhase 2

Transcranial Photobiomodulation for Executive Function in Bipolar Disorder (TPEB)

Paolo Cassano1 site in 1 country13 target enrollmentStarted: August 9, 2022Last updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
13
Locations
1
Primary Endpoint
Test the Effect of Transcranial Photobiomodulation (tPBM) on Cerebral Blood Flow (CBF)

Study Overview

Brief Summary

Transcranial light therapy, or transcranial photobiomodulation (tPBM), is a treatment that stimulates the brain by applying near-infrared light to the forehead. Transcranial light therapy has been found to promote brain metabolism, which may help improve executive function in people with bipolar disorder. The research team proposes a novel approach to treating bipolar disorder by using transcranial light therapy.

Detailed Description

This study involves a virtual screening visit, 7 in-office visits, and a virtual check-in call with a clinician. Participation will last approximately 3 weeks in total.

Participants will attend a baseline visit during which they will complete mood questionnaires and a gambling task. Participants will then receive five treatments of transcranial light therapy over one week. The first and last of these treatments will be administered while the participant is in an MRI scanner. At the first visit, participants will also receive a "sham" tPBM treatment, meaning that the device will simulate real treatment, but will not actually apply the near-infrared light. The check-in call will occur approximately 2-3 days after the final treatment visit. This will be a brief call with a study clinician to check-in on the participant's mental and physical health. The follow up visit will occur approximately one week after the final visit. Subjects will be asked to complete mood questionnaires and/or gambling tasks during the first and fifth treatment visits, as well as at the follow up visit.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
Single (Participant)

Masking Description

During the first treatment visit within the MRI, participants will receive one active tPBM treatment and one sham tPBM treatment. Participants will be blinded as to the order in which they receive these treatments.

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Adults between the ages of 18 and 65
  • •Diagnosis of bipolar disorder
  • •Currently experiencing symptoms of impulsivity
  • •Vision normal or corrected to normal with contacts

Exclusion Criteria

  • •Currently in depressive, manic, or mixed episode
  • •Currently psychotic
  • •Judged to be at serious and imminent suicidal risk
  • •Currently in alcohol or substance use disorder (meeting criteria in the past 3 months)
  • •Unstable medical conditions
  • •Inability to consent or to complete study procedures
  • •Failure to meet standard MRI safety requirements (e.g. claustrophobia, non-removable piercings, implanted medical devices, other non-removable metals)
  • •Changes in medications or use of augmentative devices and other interventions in the 2 weeks prior to the study
  • •Participation in other clinical research trials that may influence primary outcomes or adherence to the proposed study
  • •Current pregnancy.

Outcomes

Primary Outcomes

Test the Effect of Transcranial Photobiomodulation (tPBM) on Cerebral Blood Flow (CBF)

Time Frame: Day 1 of tPBM Treatment

Compare blood-oxygenation-level-dependent (BOLD) signal during sham stimulation at Day 1 versus BOLD signal during active stimulation at Day 1. Increased BOLD signal is thought to reflect increased brain activity, and thus a positive outcome. In this specific case, higher BOLD signal during active as compared to sham treatment in the right dorsolateral prefrontal cortex (rDLPFC) is thought to reflect target engagement, that is the tPBM device which is placed on the right forehead is in fact irradiating and having an effect on brain function within the rDLPFC.

Test Effect of tPBM on CBF

Time Frame: Day 1 and Day 5

Compare BOLD signal during active stimulation at Day 1 versus active stimulation at Day 5. Greater BOLD signal at Day 5 compared to Day 1 would indicate an increase in brain activity following active treatment, supporting tPBM target engagement.

Secondary Outcomes

  • Test the Effect of tPBM on Impaired Decision Making(Baseline to Follow-Up)
  • Test the Effect of Repeated t-PBM Sessions on Mood Symptoms (MOODS-SR) in Subjects With Bipolar Disorder (BD)(Baseline to Follow Up)

Investigators

Sponsor
Paolo Cassano
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Paolo Cassano

Director of Photobiomodulation

Massachusetts General Hospital

Study Sites (1)

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