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The Brain Metabolism of Unpredictable Signals

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Mass General Brigham

Status

Not yet enrolling

Conditions

Healthy

Treatments

Behavioral: (Un)predictable and (un)attended stimuli

Study type

Interventional

Funder types

Other

Identifiers

NCT05756335
2022P002851

Details and patient eligibility

About

The investigators will be studying brain glucose and oxygen metabolism using hybrid PET/fMRI imaging to better understand how decoupling between brain glucose and oxygen metabolism relates to the processing of unpredictable sensory signals.

Full description

The proposed research consists of one experiment, combining positron emission tomography (PET) and magnetic resonance imaging (MRI) techniques to simultaneously estimate the cerebral metabolic rates of glucose (CMRglc) and oxygen (CMRO2), and their ratio (oxygen:glucose index; OGI). These outcome measures will be collected in the context of a behavioral intervention presenting subjects with predictable and unpredictable stimuli, and attended and unattended stimuli. Functional PET uses a slow infusion of 2-[18F]-fluro-deoxyglucose (FDG) to estimate regional CMRglc, measuring relative changes in radiotracer uptake between blocks of task and rest. Dual-calibrated fMRI uses a sequence of hyperoxic (increased O2) and hypercapnic (increased CO2) challenges, along with a specialized sequence of MRI scans (estimating cerebral blood flow and blood-oxygen level-dependent signal) to estimate absolute CMRO2.

All subjects will be scanned, and each will complete the same behavioral intervention. First, the investigators will aim to assess the reliability of this hybrid imaging technique by having subjects complete two identical scan sessions. Second, the investigators will deliver a behavioral intervention to test the relationship between stimuli predictability, CMRglc, CMRO2, and OGI.

This experimental design is capable of producing effects observable in single subjects, and prior studies using fPET and dual-calibrated fMRI have produced effect sizes that our sample size is more than adequate to detect.

Enrollment

30 estimated patients

Sex

All

Ages

21 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults aged 21-35.
  • No contraindications to MRI or PET scanning.
  • Right-handed.
  • Fluent to speak, read, and understand English.

Exclusion criteria

  • Adults unable to consent
  • Contraindications to fMRI scanning and PET scanning (including the presence of a cardiac pacemaker or pacemaker wires, metallic particles in the body, vascular clips in the head or previous neurosurgery, prosthetic heart valves, claustrophobia)
  • Inability to lie motionless in the scanner
  • Pregnancy, seeking or suspecting pregnancy, or breastfeeding
  • History of major head trauma
  • Intracranial lesion
  • Cardiovascular disorders, including heart disorders or high blood pressure [>155/95]
  • Breathing problems such as severe asthma, emphysema, or pulmonary disease
  • Bleeding disorder, or use of anticoagulants
  • Bladder obstruction, urinary problems, or history of impaired elimination
  • Known kidney or liver problems
  • Past severe COVID-19 infection
  • Intestinal blockage
  • Raynaud syndrome
  • Anemia
  • Peripheral nerve injury
  • Diabetes
  • Glaucoma
  • Current or recent use of medications (neurological or psychiatric) affecting brain function
  • Current or past history of major medical, neurological, or psychiatric condition
  • Current or past history of chronic pain (assessed at the discretion of PI)
  • Current smoker
  • Body mass index above 35
  • Research-related radiation exposure exceeds current Radiology Department guidelines
  • Lack of current health insurance coverage
  • Employed under the direct supervision of the investigators conducting the research
  • Unwilling or unable to cooperate with breathing maneuvers required during the gas challenge
  • Respiratory or cardiac limitations to breathing at 20 L/min

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Behavioral intervention
Experimental group
Description:
Subjects are presented with a simultaneous sequence of faces and spoken words. Face stimuli include a representative sample of realistic faces across a range of ages. Spoken word stimuli are simple nouns spoken by a single female speaker.
Treatment:
Behavioral: (Un)predictable and (un)attended stimuli

Trial contacts and locations

1

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Central trial contact

Christin Y Sander, PhD; Irena Bass

Data sourced from clinicaltrials.gov

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