Trial reportJournal of neuroengineering and rehabilitation2025
Botulinum toxin A combining with robot-assisted bimanual therapy integrating mirror therapy versus botulinum toxin A combining with robot-assisted bimanual therapy in patients with post-stroke spastic fingers: a randomized controlled pilot trial.
Trial report in Journal of neuroengineering and rehabilitation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04826900 (A Randomized Control Trial to Compare the Effects Between Wearable Robotic System and Robotic Mirror Therapy in Patients With Spastic Hemiplegia Post Botulinum Toxin Injection), which is not on this map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
A Randomized Control Trial to Compare the Effects Between Wearable Robotic System and Robotic Mirror Therapy in Patients With Spastic Hemiplegia Post Botulinum Toxin Injection: Neurophysiological and Behavior Outcomes
Who cites it
2 citing papers in PubMed.
- Pulsed Radiofrequency for Post-Stroke Complications: From Neuromodulation to Functional Recovery.Current neurology and neuroscience reports · 2026Review
- Advances in the diagnosis and management of post-stroke limb spasticity: a narrative review.Frontiers in neurologyReview
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundFinger spasticity, which worsens hand function, is common in stroke patients. Botulinum toxin A (BoNT-A) treatment is effective in relieving spasticity but has little effect on arm-hand capacity. The adding of a rehabilitation program following BoNT-A injection has been suggested to enhance spasticity treatment outcomes. This pilot study aimed to compare the effects of BoNT-A combing with robot-assisted bimanual therapy (RBT) versus BoNT-A combing with RBT integrating mirror therapy (RBMT) in patients with chronic stroke and spastic fingers.
methodsPatients with chronic stroke and finger spasticity were recruited. They were randomly allocated to receive 24 training sessions of RBT or RBMT. Assessments were performed before BoNT-A injection, after 24 training sessions, and 3 months follow-up. The outcomes included Fugl-Meyer assessment for the upper extremity (FMA-UE-total, proximal and distal component scores), modified Ashworth scale (MAS), action research arm test (ARAT), box and block test (BBT), and motor activity log (MAL). We applied Friedman's test to analysis intragroup, generalized estimating equations for intergroup differences of the treatment effects.
resultsThirty-one patients were randomly allocated to the RBMT (n = 16) and RBT (n = 15) groups. After BoNT-A injection and training, both groups showed statistically significant improvements in FMA-UE total and FMA-proximal, MAS, and ARAT scores. Only the RBMT group showed significant improvements in the FMA-UE distal, and MAL scores. Neither group showed a significant improvement in the BBT. In the RBMT group the injection and post-training gains were maintained at the 3-month follow-up, except for MAS. The RBT group did not show a maintenance effect, except for the amount of use the affected UE, which showed significant improvement from baseline to follow-up. Comparing the treating effects between the two groups, there were significant differences in the FMA distal scores at post-training, favoring RBMT.
conclusionsOur pilot data demonstrated that an adjunct to BoNT-A for post-stroke spastic fingers, RBMT may provide more benefit in distal UE function than did RBT. However, a larger sample size and adding a proper control group are required to validate our findings in future studies. Trial registration This study was registered at ClinicalTrials.gov (ID no. NCT04826900, registered retrospectively on 03/28/2021).
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