2020
DOI: 10.1186/s12887-019-1904-x
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Study protocol of a randomized controlled trial of home-based computerized executive function training for children with cerebral palsy

Abstract: Background: Cerebral palsy (CP) is frequently associated with specific cognitive impairments, such as executive dysfunction which are related to participation and quality of life (QOL). The proposed study will examine whether a computerized executive function (EF) training programme could provide superior benefits for executive functioning, participation, QOL and brain plasticity, as compared to usual care. Methods: A single-blind randomized controlled trial (RCT) design will be performed. Thirty children with… Show more

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Cited by 8 publications
(6 citation statements)
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“…[30][31][32][33][34] Even current protocols, such as proposed by García-Galant et al fail to include a proper long-term assessment or follow-up. 35 Even regarding the use of invasive treatments, such as intrathecal Baclofen's or selective dorsal rhizotomy (SDR), that should actually had been better followed-up, the evidence is very scarce and insufficient. 36 Therefore, we are not able to compare our data to other results.…”
Section: Discussionmentioning
confidence: 99%
“…[30][31][32][33][34] Even current protocols, such as proposed by García-Galant et al fail to include a proper long-term assessment or follow-up. 35 Even regarding the use of invasive treatments, such as intrathecal Baclofen's or selective dorsal rhizotomy (SDR), that should actually had been better followed-up, the evidence is very scarce and insufficient. 36 Therefore, we are not able to compare our data to other results.…”
Section: Discussionmentioning
confidence: 99%
“…Given that the quality of evidence for the effectiveness of many of the included motor rehabilitation interventions varied from low to moderate, new study protocols based on rigorous methodologies might modify the recommendations formulated. [37][38][39][40][41][42][43][44]…”
Section: Strengths and Limitationsmentioning
confidence: 99%
“…Images were acquired as part of a clinical trial involving temporal lobe resection for epilepsy (n = 3 before surgery, n = 6 after surgery), glioma resection (n = 2 before surgery), or removal of arteriovenous malformations (n = 1 before surgery). This study included acquisition of a T1w MPRAGE scan (1mm isotropic, α = 9˚; TE = 2.9 ms; TI = 900 ms; TR = 1900 ms; acquisition time 4m 18s) and a modern multishell diffusion acquisition (12 @ b = 0s/mm 2 ; 20 directions @ b = 2000s/mm 2 ; 30 directions @ b = 1000s/mm 2 ; 60 directions @ b = 3000s/mm 2 ; 2mm isotropic; acquisition time 11m 30s) that is in use in a variety of studies [36][37][38]. Written informed consent was provided by all patients and the study approved by the Royal Brisbane and Women's Hospital (RBWH) Human Research Ethics Committee.…”
Section: In-vivo Experimentsmentioning
confidence: 99%