Proximal Priority Versus Distal Priority Robotic Priming Effects in Patients With Chronic Stroke

Recruiting now · Not applicable

Conditions studied: Stroke

In brief

This is a single-blind randomized comparative efficacy study involving 54-72 participants with chronic stroke. Participants will be randomized into proximal priority robotic group or distal priority robotic group and receive 18 intervention sessions (90 min/d, 3 d/wk for 6 weeks). The Fugl-Meyer Assessment Upper Extremity subscale, Medical Research Council Scale, Revised Nottingham Sensory Assessment, and Wolf Motor Function Test will be administered at baseline, after treatment, and at the 3-month follow-up. Two-way repeated-measures analysis of variance and the Chi-Square Automatic Interaction Detector Method will be used to examine the comparative efficacy and predictors of outcome, respectively, after intervention.

Key facts

Study ID
NCT04446273
Run by
National Taiwan University Hospital
People needed
72
Starts
2020-07-03
Expected to finish
2026-06-30
Last updated by the study team
2026-02-25

Who can join

Age: 20 and older, up to 75. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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