Mode
Text Size
Log in / Sign up
N/A N=9 Treatment

Pilot Study of the Feasibility and Efficacy of Working Memory Training in Children With Cochlear Implants

Bilateral Hearing Loss

Enrolled (actual)
9
Serious AEs
0.0%
Results posted
Jul 2017
Primary outcome: Primary: Digit Span Total Raw Score (Construct Measured: Verbal Short-Term/Working Memory) — 11; 11.22; 12.89; 13 Scores on a scale — p=0.766

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Cogmed Working Memory Training Program (Behavioral)
Age
Pediatric · 7+ yrs
Sex
All
Sponsor
Indiana University
Primary completion
Feb 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Digit Span Total Raw Score (Construct Measured: Verbal Short-Term/Working Memory)
11; 11.22; 12.89; 13; 11.56 0.766
PRIMARY
Spatial Span Total Raw Score (Construct Measured: Visuospatial Short-Term/Working Memory)
13; 14.33; 16.78; 16.44; 15.11 0.11
PRIMARY
Behavior Rating Inventory of Executive Function (BRIEF) - Working Memory Subscale Raw Score (Construct Measured: Behavioral Attention-Concentration and Working Memory)
16.89; 17.11; 15.33; 16.22; 16.44 0.729

Summary

This study is an investigation of the effect of a computer-based working memory training program on memory and language processing in at-risk children (e.g., those with working memory weaknesses) who have received cochlear implants.

Eligibility Criteria

Inclusion Criteria

  • age 7-16 years at the time of study enrollment,
  • profound bilateral hearing loss (> 90 dB HL in the better hearing ear),
  • implantation prior to age 3 years,
  • use of multichannel CI's,
  • a monolingual English home environment,
  • enrollment in an aural rehabilitative program that encourages the development of speaking and listening skills,
  • educational environment that uses oral or total communication (TC) strategies,
  • sufficient speech perception and language competence to complete basic word and sentence repetition tasks,
  • no significant developmental delay or neurological condition that, in the opinion of the investigators, would interfere markedly with cognitive functioning,
  • Windows-based PC at home capable of running Cogmed working memory training software,
  • mild or greater deficit in working memory, as shown by either (a) a Behavior Rating Inventory of Executive Function (BRIEF) working memory T-score of 50 or higher or (b) a Digit Span scaled score of 10 or lower. Subjects will be discontinued if during the study they have any new or changed intervention (including medication) that involves working memory, attention, concentration, or executive functioning.

Exclusion Criteria

  • Under 7 years or over 16 years of age at time of study entry
  • Implantation after age 3 years
  • Bilingual or non-English-speaking home environment
  • Primary use of American Sign Language (ASL)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00763243). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search