Actively Recruiting
Combinatory Rehabilitation Used for Substantially Helping Individuals With Traumatic Brain Injury
Led by Kessler Foundation · Updated on 2025-09-04
60
Participants Needed
1
Research Sites
253 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
New learning and memory impairment (NLMI) is a common and devastating manifestation of TBI associated with substantial life burdens. Persons with moderate to severe TBI have shown improvement in NLM for prose material (e.g. story) as well as beneficial changes in default-mode network (DMN) activation during list-learning19 following treatment with the Kessler Foundation modified Story Memory Technique® (KF-mSMT®). Benefits, however, were moderate and did not yield downstream improvements in daily life. It is thus critical to examine other approaches to complement the KF-mSMT® for robustly managing NLMI in TBI. The proposed RCT will be the first to include aerobic exercise training (AET) as a highly-promising complement to the KF-mSMT® for robustly managing NLMI, examining impact on NLM, its neural correlates, and daily life in NLM impaired persons with moderate-to-severe TBI. We thus propose a two-arm, parallel group, double-blind RCT comparing the effects of the KF-mSMT+AET with the KF-mSMT+S/T (active control condition) on NLM (Aim 1), hippocampal MRI (Aim 2), and daily life outcomes (Aim 3). 60 NLM impaired persons with moderate-to-severe TBI will be randomized to one of 2 conditions (30 per condition). Each condition will take place 3 days per week for 12 weeks and will be supervised by KF personnel. Participants will be blinded as to the intent of the conditions. We will further explore baseline predictors of clinically meaningful changes in NLM for those completing the KF-mSMT + AET condition (Exploratory Aim 4). If successful, this trial will position combinatory KF-mSMT and AET within the clinician's arsenal for robustly managing NLMI in persons with TBI. By augmenting the effects of KF-mSMT with AET, this treatment aims to exert a powerful countermeasure to TBI-related NLMI, and ultimately help those with TBI-related NLMI return to the workforce, independently manage their everyday lives, and maintain optimal quality of life. Additionally, while rigorously designed to answer the scientific question of the relative benefit of AET with the KF-mSMT, the proposed study is will likely provide some level of benefit to all study participants. If successful, this trial will provide Class I evidence of combined KF-mSMT and AET for rehabilitating NLMI in TBI, based on standards published for therapeutic trials by the American Academy of Neurology, thus positioning such an approach within the clinician's arsenal for robustly managing NLMI. By augmenting the effects of KF-mSMT with AET, we anticipate this treatment will ultimately help those with TBI-related NLMI return to the workforce, independently manage their everyday lives, and maintain optimal quality of life.
CONDITIONS
Official Title
Combinatory Rehabilitation Used for Substantially Helping Individuals With Traumatic Brain Injury
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 65 years
- Diagnosis of moderate-to-severe traumatic brain injury at least one year before enrollment
- No to low substance use or involvement as documented by ASSIST
- Insufficient physical activity with a Godin Leisure-Time Exercise Questionnaire Health Contribution Score less than 14
- Proficiency in the English language
- Right-handedness
- Approval from a physician if chronic medical conditions are present, consistent with PAR-Q+
- Ability to follow directions with a Telephone Interview for Cognitive Status (TICS-M) score of 18 or higher
- New learning and memory impairment shown by Open-Trial Selective Reminding Task scores at least 1.5 standard deviations below healthy controls
You will not qualify if you...
- Regular use of steroids or benzodiazepines
- History of neurological disorders other than traumatic brain injury
- History of severe mental illness such as schizophrenia, bipolar disorder, or severe major depression
- Presence of metal in the body, claustrophobia, or other conditions making MRI unsafe
- Moderate or high risk for exercise contraindications based on Physical Activity Readiness Questionnaire (PAR-Q+)
- Significant vision impairment including scotomas, diplopia, or nystagmus
AI-Screening
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Trial Site Locations
Total: 1 location
1
Kessler Foundation
West Orange, New Jersey, United States, 07052
Actively Recruiting
Research Team
N
Nancy Moore, MA
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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