Last reviewed · How we verify

NCT05880940: Boost

Comparing Different Rehabilitation Exercise Strategies for Improving Arm Recovery After Stroke

Completed NA Results posted Last updated 27 February 2026
What this trial tests

NA trial testing Boost - Moveable Wheelchair Armrest in Stroke in 35 participants. Completed in 28 February 2025.

Timeline
15 September 2023
Primary endpoint
31 January 2025
28 February 2025

Quick facts

Lead sponsorUniversity of California, Irvine
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment35
Start date15 September 2023
Primary completion31 January 2025
Estimated completion28 February 2025
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of California, Irvine

Who can join

Adults 18 to 84, any sex, with Stroke. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Fugl-Meyer Arm Motor Assessment Score (FMAMA) Primary · Baseline upon admission (assessed within 3 days upon admission), Post-intervention evaluation at discharge (At discharge: assessed up to 3 weeks post baseline), and 3-month post-stroke evaluation (Follow up occurred at Month 3 after Baseline)

The investigators measure the change of the Fugl-Meyer Arm Motor Assessment scores from the baseline evaluation to the 3-month post stroke follow up evaluation. Fugl-Meyer Arm Motor Assessment is a 66-point scale measuring the movement pattern of the upper extremities. The minimum score is zero and the maximum score is 66. The higher scores indicate a better outcome.

Change in score (PI - BL)
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest11.8± 6.8
Electronic Arm Exercises6.9± 6.9
Change in score (FU - BL)
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest18.6± 11.3
Electronic Arm Exercises19.2± 9.4
Modified Ashworth Spasticity Scale (MASS) Secondary · Baseline upon admission (assessed within 3 days upon admission), Post-intervention evaluation at discharge (At discharge: assessed up to 3 weeks post baseline), and 3-month post-stroke evaluation (Follow up occurred at Month 3 after Baseline)

The investigators measure the spasticity of the upper extremity at baseline, post-intervention, and at the 3-month post stroke 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.

MASS of elbow at BL
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest1.7± 1.1
Electronic Arm Exercises1.7± 1.1
MASS of elbow at PI
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest1.7± 1.3
Electronic Arm Exercises1.5± 1.1
MASS of elbow at FU
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest1.9± 1.5
Electronic Arm Exercises1.9± 1.1
MASS of wrist at BL
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest0.9± 0.9
Electronic Arm Exercises1.0± 1.1
MASS of wrist at PI
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest1.3± 1.1
Electronic Arm Exercises1.0± 0.8
MASs of wrist at FU
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest1.5± 1.1
Electronic Arm Exercises1.4± 1.0
Box and Blocks Test Secondary · Baseline upon admission (assessed within 3 days upon admission), Post-intervention evaluation at discharge (At discharge: assessed up to 3 weeks post baseline), and 3-month post-stroke evaluation (Follow up occurred at Month 3 after Baseline)

The investigators measure the Box and Blocks Test scores at baseline, post-intervention, and at 3-month post stroke 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 as a single block. The higher scores indicate a better outcome.

BBT at BL
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest3.2± 5.9
Electronic Arm Exercises1.9± 4.7
BBT at PI
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest8.2± 9.4
Electronic Arm Exercises6.7± 9.6
BBT at FU
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest16.0± 14.3
Electronic Arm Exercises22.5± 14.9
Shoulder Subluxation Distance Secondary · Baseline upon admission (assessed within 3 days upon admission), Post-intervention evaluation at discharge (At discharge: assessed up to 3 weeks post baseline), and 3-month post-stroke evaluation (Follow up occurred at Month 3 after Baseline)

The investigators measure the shoulder subluxation distance at baseline, post-intervention, and at 3-month post stroke follow up evaluation. Participants are asked to be seated in a upright chair and relax their affected upper extremity. The evaluator measures the distance, in centimeter, between the inferior aspect of the acromion and the superior aspect of the humeral head. The lower scores indicate a better outcome.

Shoulder subluxation distance at BL
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest0.6± 0.7
Electronic Arm Exercises0.6± 0.9
Shoulder subluxation distance at PT
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest0.4± 0.8
Electronic Arm Exercises0.2± 0.4
Shoulder subluxation distance at FU
GroupValue95% CI
Boost - Moveable Wheelchair Arm Rest0.5± 0.8
Electronic Arm Exercises0.3± 0.6

Sponsor's own description

The purpose of this research study is to measure the effect of participating in extra arm exercise in addition to standard rehabilitation exercises in the Acute Rehabilitation Unit. This study will compare two different ways to perform the extra arm exercise. The first is following a customized program of hand and arm exercises that will be developed for study participants by an experienced rehabilitation therapist. The second is moving a participants arm back and forth when they are sitting in their wheelchair by using a moveable wheelchair arm rest (Boost).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Stroke

Currently open trials in the same condition.

Other University of California, Irvine trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05880940.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing