跳至主要内容
临床试验/ISRCTN59250807
ISRCTN59250807已完成未知

Computerized cognitive training for pediatric patients with congenital or acquired brain injury: a home-based randomized controlled trial using the Lumosity platform

Scientific Institute (IRCCS) Eugenio Medea0 个研究点目标入组 68 人开始时间: 2017年10月25日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
68

研究概览

简要总结

2018 Results article in https://www.ncbi.nlm.nih.gov/pubmed/29924823 feasibility study results 2020 Results article in https://pubmed.ncbi.nlm.nih.gov/31996709/ preliminary results in a sample of patients (added 21/11/2023) 2023 Results article in https://pubmed.ncbi.nlm.nih.gov/37666983/ study outcome results (added 21/11/2023)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Participants are recruited among the adolescents with a congenital or acquired brain injury who had been referred to the Neurorehabilitation Units of the Scientific Institute IRCCS E. Medea in the last year. Patients with acquired brain injury are considered eligible for the study only if they are in a chronical phase (i.e., at least 1 year post-injury). For the whole sample, inclusion criteria for eligibility are:
  • 1. An age between 11 and 16 years, as in this age-range cognitive requests are generally elevated and individuals are usually able to use technological devices
  • 2. Being native Italian speakers, as in this study demonstrations and instructions on training games were provided in Italian language

排除标准

  • 1. Severe sensory or motor deficits that could not be corrected through compensatory tools and could interfere with training execution and assessment
  • 2. Being simultaneously involved in a different cognitive rehabilitation treatment, to prevent excessive demands to children and possible interference on training adherence rates
  • 3. A diagnosis of photosensitive epilepsy, as computer-based stimulation could produce negative health effects in these patients

研究者

发起方
Scientific Institute (IRCCS) Eugenio Medea

相似试验

Computerized cognitive training for pediatric... | 临床试验