Identifying Cerebral Hemodynamic Patterns in Mood Disorders and Mild Cognitive Impairment: A Functional Near-Infrared Spectroscopy (fNIRS) Study
Recruiting
Observational Study
Major Depressive DisorderBipolar DisorderMild Cognitive Impairment
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
200 (estimated)
Sponsor
Mayo Clinic · Other
Who this trial is looking for
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The purpose of this research is to measure brain activity in individuals with mood disorders and memory problems using a simple, safe, and noninvasive method called functional near-infrared spectroscopy (fNIRS). By comparing brain activity across different groups and relating it to symptom severity, this study aims to improve our understanding of how these conditions affect the brain.
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Eligibility Criteria
Inclusion Criteria
General Inclusion Criteria (across all diagnostic groups):
* 18 years and older
* Ability to provide written informed consent
* Adequate cognitive and language abilities to understand and complete study tasks, including clinical assessments and fNIRS procedures
* Confirmed clini…
Inclusion Criteria
General Inclusion Criteria (across all diagnostic groups):
* 18 years and older
* Ability to provide written informed consent
* Adequate cognitive and language abilities to understand and complete study tasks, including clinical assessments and fNIRS procedures
* Confirmed clinical diagnosis of major depressive disorder, bipolar disorder, or mild cognitive impairment (MCI)
* Stable psychiatric or cognitive condition, without acute episodes requiring immediate intervention
Specific Inclusion Criteria (for diagnostic groups):
* Healthy control
o No past or current psychiatric or cognitive disorder
* Major depressive disorder (MDD):
* Diagnosis of major depressive disorder, confirmed through clinical evaluation.
* No history of bipolar disorder or psychotic symptoms.
* Bipolar disorder:
o Diagnosis of bipolar disorder I or II, confirmed through clinical evaluation.
* Mild Cognitive Impairment (MCI):
* Pre-existing clinical diagnosis of mild cognitive impairment, supported by neuropsychological testing and/or MRI, PET scan data.
* No history of major psychiatric disorders, such as major depression, bipolar disorder or schizophrenia.
Exclusion Criteria
General Exclusion Criteria (across all diagnostic groups):
* Active primary psychotic or substance use disorders (except nicotine dependence) within the past year
* Any severe or unstable medical condition that could interfere with participation or data collection
* Any active neurological condition (including seizure disorder, traumatic brain injury, stroke) that could affect cognitive functioning or brain imaging results
* Inability to comply with study procedures, including cognitive testing, fNIRS assessment, or other assessments required by the protocol
* Pregnant women will be excluded due to potential physiological changes that could affect study outcomes
Specific Exclusion Criteria (for diagnostic groups):
* Healthy control
o Any past or current psychiatric or cognitive disorder
* Major depressive disorder (MDD):
* Diagnosis of bipolar disorder or schizophrenia.
* Brain stimulation therapy within the past 3 months.
* Bipolar disorder:
o Diagnosis of schizophrenia or schizoaffective disorder.
* Mild Cognitive Impairment (MCI):
* Diagnosis of dementia.
* Significant cognitive impairment preventing understanding or completion of study tasks.
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