scholarly journals Effect of early use of AbobotulinumtoxinA after stroke on spasticity progression: Protocol for a randomised controlled pilot study in adult subjects with moderate to severe upper limb spasticity (ONTIME pilot)

2017 ◽  
Vol 6 ◽  
pp. 9-16 ◽  
Author(s):  
Keng He Kong ◽  
Jovita Balcaitiene ◽  
Hugues Berard ◽  
Pascal Maisonobe ◽  
Khean Jin Goh ◽  
...  
2015 ◽  
Vol 37 (5) ◽  
pp. 434-440 ◽  
Author(s):  
Yanna Tong ◽  
Brian Forreider ◽  
Xinting Sun ◽  
Xiaokun Geng ◽  
Weidong Zhang ◽  
...  

2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Judith V. Graser ◽  
Caroline H. G. Bastiaenen ◽  
Urs Keller ◽  
Hubertus J. A. van Hedel

Abstract Background If adults practice several motor tasks together, random practice leads to better transfer and retention compared to blocked practice. Knowledge about this contextual interference (CI) effect could be valuable to improve neurorehabilitation of children. We present the protocol of a randomised controlled pilot study investigating the feasibility of blocked practice vs. random practice of robot-assisted upper limb reaching in children with brain lesions undergoing neurorehabilitation. Methods Children with affected upper limb function due to congenital or acquired brain lesions undergoing neurorehabilitation will be recruited for a randomised controlled pilot study with a 3-week procedure. In the control week (1), two assessment blocks (robot-assisted reaching tasks, Melbourne assessment 2, subscale fluency), 2 days apart, take place. In the practice week (2), participants are randomly allocated to blocked practice or random practice and perform 480 reaching and backward movements in the horizontal and vertical plane using exergaming with an exoskeleton robot per day during three consecutive days. Assessments are performed before, directly after and 1 day after the practice sessions. In the follow-up week (3), participants perform the assessments 1 week after the final practice session. The primary outcome is the immediate transfer of the Melbourne Assessment 2, subscale fluency. Secondary outcomes are the immediate retention, 1-day and 1-week delayed transfer and retention and acquisition during the practice sessions. We will evaluate the feasibility of the inclusion criteria, the recruitment rate, the scheduling procedure, the randomisation procedure, the procedure for the participants, the handling of the robot, the handling of the amount of data, the choice of the outcome measures and the influence of other therapies. Furthermore, we will perform a power calculation using the data to estimate the sample size for the main trial. Discussion The protocol of the pilot study is a first step towards a future main randomised controlled trial. This low risk pilot study might induce some benefits for the participants. However, we need to place its results into perspective, especially concerning the generalisability, as it remains questionable whether improving reaching constrained within a robotic device will ameliorate daily life reaching tasks. Trial registration ClinicalTrials.gov Identifier: NCT02443857


2017 ◽  
Vol 7 ◽  
pp. 179-185 ◽  
Author(s):  
Sarah R. Valkenborghs ◽  
Milanka M. Visser ◽  
Ashlee Dunn ◽  
Kirk I. Erickson ◽  
Michael Nilsson ◽  
...  

2017 ◽  
Vol 6 (94) ◽  
pp. 6877-6880
Author(s):  
Naorem Bimol ◽  
Yumnam Ningthemba Singh ◽  
Taha Peya ◽  
Yumnam Nandabir Singh ◽  
Akoijam Joy Singh ◽  
...  

Toxins ◽  
2018 ◽  
Vol 10 (7) ◽  
pp. 253 ◽  
Author(s):  
Raymond Rosales ◽  
Jovita Balcaitiene ◽  
Hugues Berard ◽  
Pascal Maisonobe ◽  
Khean Goh ◽  
...  

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Judith V. Graser ◽  
Caroline H. G. Bastiaenen ◽  
Anja Gut ◽  
Urs Keller ◽  
Hubertus J. A. van Hedel

Abstract Introduction Evidence about contextual interference in children with brain lesions when practising motor tasks is lacking. Our main objective was to evaluate the feasibility of a randomised controlled trial (RCT) comparing blocked with random practice order of an upper limb robotic exergame to improve reaching in children with neuromotor disorders with a pilot trial. Methods We recruited children with brain lesions and impaired upper limb functions who underwent a 3-week schedule that consisted of baseline assessments, intervention period (participants were randomised to a blocked or random order group), and follow-up assessment. We evaluated ten feasibility criteria, including the practicability of the inclusion/exclusion criteria, recruitment rate, feasibility of randomisation, scheduling procedure, and the participants’ programme adherence. Results The inclusion/exclusion criteria were not completely feasible as patients who were not able to perform the exergames were included. Twelve participants were recruited, and six datasets were used for analysis. The scheduling and randomisation procedures were generally feasible, but the procedure was only partially feasible for the participants, as some sessions were aborted due to lack of motivation and fatigue. Conclusion An RCT following this study protocol is not feasible. We formulated suggestions for future studies that aim to investigate contextual interference as in this pilot study. Trial registration ClinicalTrials.gov Identifier: NCT02443857, registered on May 14, 2015


Author(s):  
Federico Posteraro ◽  
Simona Crea ◽  
Stefano Mazzoleni ◽  
Mihai Berteanu ◽  
Ileana Ciobanu ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document