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Combinatory Rehabilitation Used for Substantially Helping Individuals With Traumatic Brain Injury (CRUSH-IT)

Primary Purpose

Traumatic Brain Injury

Status
Recruiting
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
KF-mSMT Plus Aerobic Exercise Training
KF-mSMT Plus Stretching Exercise Training
Sponsored by
Kessler Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traumatic Brain Injury

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age between 18-65 to control for age related brain changes Diagnosis of moderate-to-severe TBI based on TBIMS criteria at least one year prior to enrollment Having no to low substance use / involvement (drug/alcohol) as documented via ASSIST Being insufficiently physically active based on a Godin Leisure-Time Exercise Questionnaire Health Contribution Score of <14 Having a proficiency in the English language Being right handed to control for brain organization Having chronic medical conditions (e.g. diabetes) in addition to TBI will require approval to participate from a physician, consistent with PAR-Q+. Having an in-tact ability to follow directions based on the Telephone Interview for Cognitive Status (TICS-M) (i.e., TICS-M scores of ≥18) Demonstrating new learning and memory impairment based on Open-Trial Selective Reminding Task (OT-SRT) scores at least 1.5 standard deviations below healthy controls (8+ trials to reach criterion) Exclusion Criteria: Regularly taking steroids & benzodiazapines to control for medications effects Having a history of neurological disorders beyond TBI Having a history of severe mental illness (e.g., schizophrenia, bipolar, severe major depression) Having metal in the body, claustrophobia, and other risk factors that would make MRI scanning unsafe. Having moderate or high risk for exercise training contraindications (e.g. diabetes), defined as ≥1 YES on pages 2-3 of the Physical Activity Readiness Questionnaire for Everyone (PAR-Q+) Having significantly impaired vision by scotomas (corrected vision in worse eye worse than 20/60), diplopia, or nystagmus.

Sites / Locations

  • Kessler FoundationRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

KF-mSMT Plus Aerobic Exercise Training

KF-mSMT Plus Stretching Exercise Training

Arm Description

Participants will undergo 12 weeks of supervised aerobic cycling exercise training. During the last 8 weeks of cycling exercise, participants will also undergo treatment with the Kessler Foundation modified Story Memory Technique as an approach for cognitive rehabilitation.

Participants will undergo 12 weeks of supervised stretching and toning exercise training. During the last 8 weeks of stretching exercise, participants will also undergo treatment with the Kessler Foundation modified Story Memory Technique as an approach for cognitive rehabilitation.

Outcomes

Primary Outcome Measures

Change in California Verbal Learning Test-3 Performance
This is a test of new learning and memory

Secondary Outcome Measures

Change in hippocampal volume
This involves a structural MRI scan wherein the volume of the bilateral hippocampi will be measured.
Change in hippocampal activation
This involves an fMRI list-learning task wherein activation of the hippocampus during encoding and recall will be measured
Change in hippocampal resting-state functional connectivity
This involves a resting-state fMRI paradigm wherein connectivity between the hippocampus and other brain regions that are important for learning and memory will be measured.
Change in Everyday Memory Simulations Performance
This multi-component test examines aspects of memory that are relevant to daily life.

Full Information

First Posted
January 13, 2023
Last Updated
June 7, 2023
Sponsor
Kessler Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT05716048
Brief Title
Combinatory Rehabilitation Used for Substantially Helping Individuals With Traumatic Brain Injury
Acronym
CRUSH-IT
Official Title
Randomized Controlled Trial of Combined Cognitive Rehabilitation and Exercise Training for Learning and Memory in Persons With Moderate to Severe Traumatic Brain Injury
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 21, 2023 (Actual)
Primary Completion Date
February 28, 2028 (Anticipated)
Study Completion Date
February 28, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kessler Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
KF-mSMT Plus Aerobic Exercise Training
Arm Type
Experimental
Arm Description
Participants will undergo 12 weeks of supervised aerobic cycling exercise training. During the last 8 weeks of cycling exercise, participants will also undergo treatment with the Kessler Foundation modified Story Memory Technique as an approach for cognitive rehabilitation.
Arm Title
KF-mSMT Plus Stretching Exercise Training
Arm Type
Active Comparator
Arm Description
Participants will undergo 12 weeks of supervised stretching and toning exercise training. During the last 8 weeks of stretching exercise, participants will also undergo treatment with the Kessler Foundation modified Story Memory Technique as an approach for cognitive rehabilitation.
Intervention Type
Behavioral
Intervention Name(s)
KF-mSMT Plus Aerobic Exercise Training
Intervention Description
Participants will undergo this combinatory intervention 3 days per week for 12 weeks. The combined session duration will begin with 15 minutes and last up to 2 hours by the end of the 12th week
Intervention Type
Behavioral
Intervention Name(s)
KF-mSMT Plus Stretching Exercise Training
Intervention Description
Participants will undergo this combinatory intervention 3 days per week for 12 weeks. The combined session duration will begin with 15 minutes and last up to 2 hours by the end of the 12th week
Primary Outcome Measure Information:
Title
Change in California Verbal Learning Test-3 Performance
Description
This is a test of new learning and memory
Time Frame
From 0 to 12 weeks
Secondary Outcome Measure Information:
Title
Change in hippocampal volume
Description
This involves a structural MRI scan wherein the volume of the bilateral hippocampi will be measured.
Time Frame
From 0 to 12 weeks
Title
Change in hippocampal activation
Description
This involves an fMRI list-learning task wherein activation of the hippocampus during encoding and recall will be measured
Time Frame
From 0 to 12 weeks
Title
Change in hippocampal resting-state functional connectivity
Description
This involves a resting-state fMRI paradigm wherein connectivity between the hippocampus and other brain regions that are important for learning and memory will be measured.
Time Frame
From 0 to 12 weeks
Title
Change in Everyday Memory Simulations Performance
Description
This multi-component test examines aspects of memory that are relevant to daily life.
Time Frame
From 0 to 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18-65 to control for age related brain changes Diagnosis of moderate-to-severe TBI based on TBIMS criteria at least one year prior to enrollment Having no to low substance use / involvement (drug/alcohol) as documented via ASSIST Being insufficiently physically active based on a Godin Leisure-Time Exercise Questionnaire Health Contribution Score of <14 Having a proficiency in the English language Being right handed to control for brain organization Having chronic medical conditions (e.g. diabetes) in addition to TBI will require approval to participate from a physician, consistent with PAR-Q+. Having an in-tact ability to follow directions based on the Telephone Interview for Cognitive Status (TICS-M) (i.e., TICS-M scores of ≥18) Demonstrating new learning and memory impairment based on Open-Trial Selective Reminding Task (OT-SRT) scores at least 1.5 standard deviations below healthy controls (8+ trials to reach criterion) Exclusion Criteria: Regularly taking steroids & benzodiazapines to control for medications effects Having a history of neurological disorders beyond TBI Having a history of severe mental illness (e.g., schizophrenia, bipolar, severe major depression) Having metal in the body, claustrophobia, and other risk factors that would make MRI scanning unsafe. Having moderate or high risk for exercise training contraindications (e.g. diabetes), defined as ≥1 YES on pages 2-3 of the Physical Activity Readiness Questionnaire for Everyone (PAR-Q+) Having significantly impaired vision by scotomas (corrected vision in worse eye worse than 20/60), diplopia, or nystagmus.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nancy Moore, MA
Phone
973-324.8450
Email
nbmoore@kesslerfoundation.org
Facility Information:
Facility Name
Kessler Foundation
City
West Orange
State/Province
New Jersey
ZIP/Postal Code
07052
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brian M Sandroff, PhD

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Combinatory Rehabilitation Used for Substantially Helping Individuals With Traumatic Brain Injury

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