MRI Markers of Feedback Timing During Learning in Individuals With TBI With and Without Clinical Depression

Sponsor

Kessler Foundation (Other)

Overall Status

Recruiting

CT.gov ID

NCT05009511

Collaborator

National Institute of Neurological Disorders and Stroke (NINDS) (NIH), Moss Rehabilitation Research Institute (Other)

180

Enrollment

Location

Arms

Anticipated Duration (Months)

3.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The goal of this proposal is to examine the influence of feedback timing on learning and brain function in individuals with moderate-to-severe traumatic brain injury (TBI), with and without depression.

Condition or Disease	Intervention/Treatment	Phase
Traumatic Brain Injury Major Depressive Disorder	Behavioral: Learning through feedback	N/A

Detailed Description

The overall objective of the proposed project is to investigate brain mechanisms during learning in individuals with traumatic brain injury (TBI) with and without clinical depression. Such knowledge can help guide rehabilitation strategies and reduce the burden of TBI. Feedback about the accuracy of one's actions can improve learning by informing an individual whether his/her action is correct or not. Individuals with depression have been shown to have learning deficits and altered brain activity during learning compared to healthy individuals when feedback is presented immediately. Impaired learning through immediate feedback has also been observed in Parkinson's disease (PD) patients. However, PD patients are able to learn from feedback when it is presented after a delay, engaging separate neural mechanisms. Individuals with TBI have also been shown to have learning deficits that are likely exacerbated by depressive symptoms. However, there is no evidence directly examining the neural mechanisms of learning in individuals with TBI with and without depression. The proposed research explores this distinction.

The elucidation of the neural mechanisms associated with learning in individuals with TBI with and without clinical depression will inform 1) scientific knowledge about the effect of depression on the injured brain, 2) TBI interventions about the effectiveness of feedback and its timing, and 3) interventions for other clinical populations that require rehabilitation and have high occurrence of depression. These objectives lie at the heart of the mission of the National Institute of Neurological Disorders and Stroke as they will broaden "fundamental knowledge about the brain and nervous system" associated with learning in TBI and the knowledge gained from fulfilling the above objectives will "reduce the burden" of learning deficits after TBI.

To test these hypotheses, participants will be recruited based on structured clinical interview performed by the team member trained in psychiatric interviewing. Qualified participants will perform an experiment during which they will first study word pairs outside of the functional magnetic resonance imaging scanner. Then, in the scanner, participants will see word pairs again in a multiple-choice format and will have to choose a match for each word. After participants make their choice, feedback will be presented either immediately or after a delay of 25 minutes. The experiment will end with the Test phase, which takes place outside of the scanner, where participants will be presented with the words in the multiple-choice format again so the influence of each feedback type on learning can be evaluated.

Investigators hypothesize that depressed individuals with and without TBI will learn better from delayed compared to immediate feedback, because learning through delayed feedback relies on a different neural mechanism, which is not affected by depression and TBI, compared to learning through immediate feedback. Non-depressed individuals without TBI and clinically depressed individuals without TBI will also be recruited to delineate the influences of depression from the impact of TBI on the brain.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

180 participants

Allocation:

Randomized

Intervention Model:

Single Group Assignment

Masking:

Single (Investigator)

Primary Purpose:

Basic Science

Official Title:

MRI Markers of Feedback Timing During Learning in Individuals With TBI With and Without Clinical Depression

Actual Study Start Date :

Sep 1, 2021

Anticipated Primary Completion Date :

Jan 31, 2026

Anticipated Study Completion Date :

Jan 31, 2026

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Traumatic Brain Injury (TBI) Individuals with moderate-to-severe injury severity, defined as post-traumatic amnesia lasting more than 24hrs, loss of consciousness lasting more than 30 min, Glasgow Coma Scale (GCS) score less than 13.	Behavioral: Learning through feedback The goal of this investigation is to examine the influence of feedback timing on learning and brain function.
Experimental: Traumatic Brain Injury (TBI) with MDD Individuals with moderate-to-severe injury severity, defined as post-traumatic amnesia lasting more than 24hrs, loss of consciousness lasting more than 30 min, Glasgow Coma Scale (GCS) score less than 13. In addition, individuals will have a diagnosis of major depressive disorder (MDD) as per DSM-5.	Behavioral: Learning through feedback The goal of this investigation is to examine the influence of feedback timing on learning and brain function.
Experimental: Major Depressive Disorder (MDD) Individuals meeting criteria for major depressive disorder (MDD) including qualifiers 'in partial remission' or 'in full remission' if they are actively in treatment for the condition and still carry the depression diagnosis.	Behavioral: Learning through feedback The goal of this investigation is to examine the influence of feedback timing on learning and brain function.
Experimental: Healthy Individuals Healthy individuals without psychiatric and neurological conditions.	Behavioral: Learning through feedback The goal of this investigation is to examine the influence of feedback timing on learning and brain function.

Outcome Measures

Primary Outcome Measures

Learning accuracy [Collected during the single 1 day study]
Participants' learning accuracy (in percent) assessed with Eprime software
functional MRI [Collected during the single 1 day study]
Participants brain activity

Secondary Outcome Measures

Verbal Paired Associates test [Collected during the single 1 day study]
Verbal learning and memory assessment
Logical Memory test [Collected during the single 1 day study]
Verbal learning and memory assessment
Delis-Kaplan Executive Function System [Collected during the single 1 day study]
Executive functioning assessment
Test of Premorbid Functioning [Collected during the single 1 day study]
Pre-morbid cognitive and memory functioning assessment
Ruff 2 & 7 Selective Attention Test [Collected during the single 1 day study]
Attention Assessment
Wechsler Adult Intelligence Scale, 4th edition [Collected during the single 1 day study]
Working memory/processing assessment
Behavioral Inhibition/Behavioral Approach Scale [Collected during the single 1 day study]
Questionnaire
GAD [Collected during the single 1 day study]
Questionnaire
PCL [Collected during the single 1 day study]
Questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 65 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

I am between the ages of 18 and 65.
I have been diagnosed with a TBI.
I am an individual without TBI.
I am right-handed.
I have normal vision or corrected to normal vision.
I can read and speak English fluently.
I do or do not have a current diagnosis of Depression.
I am not currently pregnant.

Exclusion Criteria:

I have had a neurological disease, other than TBI.
I have a significant history of alcohol or drug abuse as determined by study staff.
I have metal in my body (shrapnel, piercing that cannot be taken off, retainer on the upper jaw).
I have something in my body that restricts me from having an MRI such as: an aneurysm clip; implanted neural stimulator; implanted cardiac pacemaker or auto-defibrillator; cochlear implant (internal hearing aids); ocular foreign body (e.g. metal shavings in my eye), insulin pump or any pre- existing eye conditions (such as blurry vision, seeing double, and abnormal eye movements).
I experience discomfort in closed spaces (claustrophobia).
I have been diagnosed with a neurologic illness such as epilepsy, brain tumors, etc. (e.g. schizophrenia and bipolar disorder).
I have had corticosteroid treatment less than a month ago as determined by study staff review of my medications.
I have been informed by my doctor that is it unsafe for me to receive regular MRI as part of my medical care.