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Clinical Trials/NCT04206475
NCT04206475
Completed
Not Applicable

Feasibility Randomized Trial for an Intensive Memory-Focused Training Program for School Aged Children With Acquired Brain Injury.

IRCCS Eugenio Medea1 site in 1 country21 target enrollmentOctober 21, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acquired Brain Injury
Sponsor
IRCCS Eugenio Medea
Enrollment
21
Locations
1
Primary Endpoint
Psychometric evaluation
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Memory deficits are common sequelae of pediatric Acquired Brain Injury (ABI). Only methods for non-focused cognitive remediation are available to the pediatric field. The aims of this feasibility trial are the description, implementation, and test of an intensive program specific to the training and re-adaptation of memory function in children (IM-FTP). Method: Eleven children and adolescents with ABI (mean age at injury=12.2 years, brain tumor survivors excluded) were clinically assessed and rehabilitated over 1-month through IM-FTP, including physio-kinesis/occupational, speech, and neuropsychology treatments. Each patient received a psychometric evaluation and a brain functional MRI at enrollment and at discharge. Ten pediatric controls with ABI (mean age at injury=13.8 years) were clinically assessed, and rehabilitated through a standard program.

Registry
clinicaltrials.gov
Start Date
October 21, 2013
End Date
February 3, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
IRCCS Eugenio Medea
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • i) age at first assessment between 6 and 18 years;
  • ii) time between injury and first assessment \<3 months;
  • iii) documented evidence of a severe ABI of traumatic or non-traumatic (i.e. anoxic, vascular or infectious) etiology, as indicated by a Glasgow Coma Scale (GCS, \[26\]), score ≤8 at insult;
  • iv) presence of severe memory impairment, as assessed at first evaluation;
  • v) sufficient attentive skills for attending a simple task and understanding simple commands/directions, and sufficient verbal comprehension for executing simple procedures/exercises;
  • vi) absence of congenital pathology or disability previous to the injury;
  • vii) medical records sufficiently detailed to determine the injury severity and neurological findings;
  • viii) absence of severe motor or sensitive deficits.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Psychometric evaluation

Time Frame: 4 weeks

At both time points, the patients were administered the Rey- Osterrieth complex figure test (REY), the test for immediate and delayed memory of a list of words of the Italian 'Batteria di Valutazione Neuropsicologica' (BVN) battery (BVNLi and BVNLd, respectively), the test for immediate and delayed recall in prose memory of the Italian BVN battery (BVNPi and BVNPd), the test for immediate and delayed recall in positional memory supra-span (SUPRASPANi and SUPRASPANd), and the Italian TEMA test for the learning of couples of related and unrelated words (TEMA)

Study Sites (1)

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