The Promotoer, a brain-computer interface-assisted intervention to promote upper limb functional motor recovery after stroke: a statistical analysis plan for a randomized controlled trial

被引:2
|
作者
Cipriani, Marta [1 ,2 ]
Pichiorri, Floriana [3 ]
Colamarino, Emma [3 ,4 ]
Toppi, Jlenia [3 ,4 ]
Tamburella, Federica [3 ]
Lorusso, Matteo [3 ]
Bigioni, Alessandra [3 ]
Morone, Giovanni [3 ]
Tomaiuolo, Francesco [5 ]
Santoro, Filippo [6 ]
Cordella, Daniele [7 ]
Molinari, Marco [3 ]
Cincotti, Febo [3 ,4 ]
Mattia, Donatella [3 ]
Puopolo, Maria [1 ]
机构
[1] Ist Super Sanita, Dept Neurosci, Rome, Italy
[2] Sapienza Univ Rome, Dept Stat Sci, Rome, Italy
[3] Fdn Santa Lucia, IRCCS, Rome, Italy
[4] Sapienza Univ Rome, Dept Comp Control & Management Engn Antonio Rubert, Rome, Italy
[5] Univ Messina, Dept Clin & Expt Med, Messina, Italy
[6] Ist Super Sanita, Res Coordinat & Support Serv, Rome, Italy
[7] Ist Super Sanita, IT Serv, Rome, Italy
关键词
EEG-based brain-computer interface; Stroke; Hand functional motor recovery; Neurorehabilitation; Randomized controlled trial; Statistical analysis plan; REHABILITATION; METHODOLOGY; IMPAIRMENT; EFFICIENCY;
D O I
10.1186/s13063-023-07773-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundElectroencephalography (EEG)-based brain-computer interfaces (BCIs) allow to modulate the sensorimotor rhythms and are emerging technologies for promoting post-stroke motor function recovery. The Promotoer study aims to assess the short and long-term efficacy of the Promotoer system, an EEG-based BCI assisting motor imagery (MI) practice, in enhancing post-stroke functional hand motor recovery. This paper details the statistical analysis plan of the Promotoer study.MethodsThe Promotoer study is a randomized, controlled, assessor-blinded, single-centre, superiority trial, with two parallel groups and a 1:1 allocation ratio. Subacute stroke patients are randomized to EEG-based BCI-assisted MI training or to MI training alone (i.e. no BCI). An internal pilot study for sample size re-assessment is planned. The primary outcome is the effectiveness of the Upper Extremity Fugl-Meyer Assessment (UE-FMA) score. Secondary outcomes include clinical, functional, and user experience scores assessed at the end of intervention and at follow-up. Neurophysiological assessments are also planned. Effectiveness formulas have been specified, and intention-to-treat and per-protocol populations have been defined. Statistical methods for comparisons of groups and for development of a predictive score of significant improvement are described. Explorative subgroup analyses and methodology to handle missing data are considered.DiscussionThe Promotoer study will provide robust evidence for the short/long-term efficacy of the Promotoer system in subacute stroke patients undergoing a rehabilitation program. Moreover, the development of a predictive score of response will allow transferring of the Promotoer system to optimal clinical practice. By carefully describing the statistical principles and procedures, the statistical analysis plan provides transparency in the analysis of data.Trial registrationClinicalTrials.gov NCT04353297. Registered on April 15, 2020.
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页数:11
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