Skip to main content
OpenTrials
Completed

NCT Number: NCT02830893

Efficacy Study of the LARA Wheelchair System for Subacute Stroke Patients

This study will test the effectiveness of a new lever drive wheelchair, LARA - Lever Actuated Resonance Assistance. LARA facilitates patients in performing a high amount of practice using their moderate to severely impaired upper extremity after stroke.

Investigators will recruit 44 subjects with subacute strokes to participate in the study through the acute rehabilitation unit of the UC Irvine Douglas Hospital. Study participants will be randomized into 2 groups: LARA therapy group or standard therapy group. The LARA therapy group will use LARA to propel themselves to therapy appointments in the unit and to play video games with the affected upper extremity for 30 mins / day. The standard therapy group will use a standard wheelchair to propel themselves using their unaffected upper and lower extremities. They will be asked to perform a matched duration of standard arm exercises for 30 mins/ day. This program of standard arm exercises was developed by an OT at the Rehabilitation Institute of Chicago which consists of graded-difficulty table-supported exercises.

This study will have 3 assessment visits: baseline, 3 weeks after therapy or upon discharge from the acute rehabilitation unit if sooner, and a 3-month follow up.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Cerebrovascular Accident Brain Diseases Cardiovascular Diseases Central Nervous System Diseases Cerebrovascular Disorders Nervous System Diseases Stroke Vascular Diseases

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of California, Irvine

Irvine, California, 92697, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years at the time of enrollment
  • Stroke onset 1-4 weeks prior to study enrollment
  • Arm motor FM score of < 30 (out of 66) at Baseline Visit
  • Absence of moderate to severe shoulder pain ( Score <3 on the 10 point visual analog pain scale)
  • Any deficit in vision, alertness, language, attention, or other cognitive functions that interfere with playing the LARA games

Exclusion criteria

  • Age >80 years at the time of enrollment
  • Severe tone in the affected upper extremities (Score ≥ 4 on the Modified Ashworth Spasticity Scale)
  • Severe language problem that would prevent participants from properly understanding instructions
  • Severe reduced level of consciousness
  • Severe aphasia (score of 3 on the NIH stroke scale (question 9))
  • Severe loss of sensation in stroke-affected upper extremities (Score < 1 on the Nottingham sensory assessment)
  • Currently pregnant
  • Difficulty in understanding or complying with the instructions given by the experimenter
  • Inability to perform the experimental task that will be studied

Treatment and study plan

LARA

Device

Study participants will use LARA to propel themselves and to play computer games with the impaired upper extremity for 30 min/day in addition to standard of care rehabilitation therapy for 3 weeks or the duration of their stay.

Standard

Behavioral

Study participants will receive no exposure to LARA, will use a standard wheelchair, and will be asked to perform a program of conventional arm exercises for 30 min/day, also in addition to standard of care rehabilitation therapy for 3 weeks or the duration of their stay.

Other names: Conventional Arm and Hand Exercise Program

Primary outcomes

  1. Fugl-Meyer (FM) Motor Assessment of the Upper Extremity

    Time frame: Baseline, Post-intervention evaluation at 3 weeks, and 3-month evaluation after the end of intervention

    We measure the change of the Fugl-Meyer Motor Assessment scores from the baseline evaluation to the 3-month follow up evaluation after the end of intervention. Fugl-Meyer is a 66-point scale measuring the movement pattern of the upper extremities. For the study, we analyze the total score only. The higher scores indicate a better outcome.

Secondary outcomes

  1. Modified Ashworth Spasticity Scale

    Time frame: Baseline, Post-intervention evaluation at 3 weeks, and 3-months after the end of intervention

    We measure the spasticity of the upper extremity at baseline, post-intervention, and at the 3-month follow up evaluation. Spasticity is described as the resistance to passive movement. Participants are asked to relax and evaluators assess muscle resistance to passive movement at one joint at a time: Shoulder, Elbow, Wrist, and Fingers. The evaluator will then grade the resistance on a 6-point scale for each joint. Higher scores indicate more rigid movement or more muscle tone resistance. The minimum score is zero and the maximum score is 4. For this study, we combine all subscores from each joint to compute a total spasticity score.

  2. Timed 10-meter Walk

    Time frame: Baseline, Post-intervention evaluation at 3 weeks, and 3-months after the end of intervention

    We measure the time one takes to complete a 10-meter walk at baseline evaluation, the post-intervention evaluation, and the 3-month follow up evaluation. Participants are instructed to walk at a distance of 10-meter over a level surface with 2 meters for acceleration and 2 meters for deceleration. Participants are instructed to walk at their comfortable or normal speed over the entire distance. Participants are timed once the first foot passes the acceleration path; the time is stopped once the first foot enters the deceleration path. The lower scores indicate a better outcome.

  3. Box and Blocks Test

    Time frame: Baseline, Post-intervention evaluation at 3 weeks, and 3-months after the end of intervention

    We measured the Box and Blocks Test scores at baseline evaluation, the post-intervention, and at the 3-month follow up evaluation. Participants are instructed to move as many blocks as possible, one at a time, from one compartment in a box to a second compartment over a divider for a period of 60 seconds; each block that is moved is counted, and multiple blocks moved at the same time are counted are counted as a single block. The higher scores indicate a better outcome.

Sponsors and collaborators

Lead sponsor

University of California, Irvine

Other

Registry information

Official study title

Lever Actuated Rehabilitation of the Arm Using Wheelchair Propulsion and Computer Gaming

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Jul 13, 2016
Registry last updated
Jul 21, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.