The Brave Initiative: Bringing Rehabilitation to American Veterans in an Enriched Environment (TBI)
Traumatic Brain Injury
About this trial
This is an interventional treatment trial for Traumatic Brain Injury focused on measuring Constraint-Induced Movement Therapy, Physical Therapy, Rehabilitation, Occupational Therapy, Fitness Training, Recovery of Function, Neuroplasticity, Exercise Therapy, Brain Injuries, Traumatic Brain Injury, Physical Therapy Modalities, Neuroimaging
Eligibility Criteria
Inclusion Criteria:
- Motor criteria will be made using an impairment-level system for characterizing the severity of an upper-extremity (UE) motor deficit based on Active Range of Motion (AROM). All UE motor criteria determinations will be made with the subject sitting. The more-affected forearm will be resting on a supporting surface (e.g. arm of chair) to allow for maximum wrist flexion with gravity. This study will treat patients at levels of Grade 2 (mild/moderate impairment) and Grade 3 (moderate impairment).
The minimum motor criterion (MMC) for inclusion in Grade 3 (moderate impairment) will be ability to:
- Extend against gravity at least 10 degrees at the wrist from a fully flexed starting position
- Extend two or more fingers at least 10 degrees at the metacarpophalangeal (MP) joint and either the proximal or distal interphalangeal (IP) joints
- Extend or abduct the thumb at least 10 degrees
- Extend the elbow at least 20 degrees from a 90 degree flexed starting position
- Flex and abduct the shoulder at least 45 degrees
The MMC for inclusion in Grade 2 (mild/moderate impairment) will be ability to:
- Extend against gravity at least 20 degrees at the wrist from a fully flexed starting position
- Extend all fingers at least 10 degrees at the MP joint and either the proximal or distal IP joints
- Extend or abduct the thumb at least 10 degrees
- Extend the elbow at least 20 degrees from a 90 degree flexed starting position
- Flex and abduct the shoulder at least 45 degrees
- Additionally, subjects must have substantially reduced use of the extremity in the activities of daily living as indicated by a score of less than 2.5 on the Motor Activity Log (MAL).
Note: Each movement described above must be repeated 3 times in 1 minute.
Exclusion Criteria:
- Those < 3 months post-TBI.
- Excessive UE spasticity.
- Insufficient stamina to carry out the requirements of the therapy (based on clinical judgment).
Medication (including psychoactive substances) will not be exclusionary except in the following cases: (If subjects are on other medications, the medications will be recorded and the possible effect on treatment outcome will be analyzed separately)
- Participation in any experimental drug field study
- Botox injections to the more-affected UE less than 3 months prior to participation
- Baclofen or Dantrium taken orally at the time of study
- Mini-Mental Status Exam (MMSE) score below 20.
- Concurrent participation in any formal physical rehabilitation program or clinical trial.
- Excessive pain in any joint of the more-affected extremity that could limit ability to cooperate with the intervention (based on clinical judgment).
- Serious, uncontrolled medical problems (e.g., cardiovascular, severe rheumatoid arthritis, serious joint deformity of arthritic origin, symptomatic cancer or renal disease, any kind of end-stage pulmonary or cardiovascular disease, uncontrolled epilepsy) as judged by the Medical Director.
- Other neurological or musculoskeletal conditions affecting UE function.
- Unable to read or speak English.
- Inadequate communication skills, i.e., not able to reliably understand questions or not able to express needs or report own behavior, to participate in study based on clinical judgment.
- Substantial use of the more-affected arm in daily life as reflected by a Motor Activity Log score > 2.5.
- Pain that interferes with use of the more-affected arm based on clinical judgment.
- A positive pregnancy test will exclude participants from MRI scanning, but would not exclude them from clinical treatment.
Sites / Locations
- University of Alabama at Birmingham
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Active Comparator
Active Comparator
Standard CI Therapy Group
Enhanced CI Therapy Group
Standard Fitness Training Group
Enhanced Fitness Training Group
This group will receive Constraint-Induced Movement Therapy (CIMT) with the Standard Transfer Package (sTP).
This group will receive CIMT with the enhanced Transfer Package (eTP).
This group will receive Lakeshore Enriched Fitness Training (LEFT) with the standard Transfer Package (sTP).
This group will receive LEFT with the enhanced Transfer Package (eTP)