BURT Efficacy in Improving Upper Extremity Strength and Function During Post-stroke Inpatient Rehabilitation
Stroke, Stroke, Acute, Cerebral Vascular Accident
About this trial
This is an interventional treatment trial for Stroke focused on measuring BURT, Upper extremity function, Inpatient rehabilitation, Upper extremity robotics
Eligibility Criteria
Inclusion Criteria:
- Inpatient at Sunnyview Rehabilitation Hospital
- >/= 18 years
- Unilateral stroke affecting dominant side
- UE paresis affected arm with 3-/5 or less manual muscle testing throughout
Exclusion Criteria:
>30 days post stroke
- Severe Neglect
- Bilateral stroke
- Prior stroke with residual deficits
- Patients receiving prism adaptation treatment
- Comorbid neurological disorders
- Upper limb comorbidities that could limit functional improvement (UE arthritis pain, UE fracture, fixed contracture not allowing for proper device alignment)
- Severe shoulder subluxation that cannot be accommodated by the device
- Severe osteoporosis
- Unable to follow simple directions
- Unable to tolerate sitting 30 minutes
- Expected length of stay (LOS) < 15 days.
Sites / Locations
- Gaylord Hospital
- Sunnyview Rehabilitation HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Conventional Upper Extremity Neuroeducation
BURT Upper Extremity
74 patients will receive the standard occupational therapy sessions that they would normally receive during their IRF stay. UE neuroeducation sessions are typically focused on improving strength and mobility of the upper arm. Clinicians will not be given instructions on how to run their sessions, however they will not be allowed to use BURT. Other devices that would normally be used during neuro-educational sessions (including X-cite, electrical stimulation and RT-300) will be allowed for use in this group. The therapists will track the activity, level of assistance and time provided in a tracking sheet, as well as document any adverse events that may occur
As part of routine therapy, 74 patients will receive up to 5 sessions per week of BURT UE therapy in place of conventional neuro re-education. Patients in this arm of the study will receive any conventional therapy during the remainder of their treatment sessions. When using BURT, therapists will track the activity, level of assistance and time provided in a tracking sheet, as well as document any adverse events that may occur.