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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01663454
Other study ID # bhø_2011/2271
Secondary ID
Status Completed
Phase N/A
First received August 9, 2012
Last updated October 7, 2014
Start date September 2012
Est. completion date December 2012

Study information

Verified date October 2014
Source Helse Stavanger HF
Contact n/a
Is FDA regulated No
Health authority Norway: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this pilot study is to assist the preparation of a larger multi-center study. The main aim is to determine the feasibility of conducting computerized working memory training in a group of children with cerebral palsy.


Recruitment information / eligibility

Status Completed
Enrollment 6
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 7 Years to 8 Years
Eligibility Inclusion Criteria:

- Born at term with unilateral spastic CP

- Born preterm with bilateral spastic CP

Exclusion Criteria:

- Children with Gross Motor Function Classification Scale (GMFCS) level V

- Severe visual or hearing impairments

- Photosensitive epilepsy

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Cogmed Robomemo working memory training
The Cogmed Robomemo program is designed as a computer game in which an animated robot gives different tasks to be solved by the child. The tasks have various degrees of difficulty adapted continuously throughout the intervention period to the performance of the individual child. The program is standardized in that each child receives the same set of tasks during the training period. The child will perform the training sessions at home using their own computer for about 35-40 minutes each day.

Locations

Country Name City State
Norway Stavanger University Hospital Stavanger

Sponsors (1)

Lead Sponsor Collaborator
Helse Stavanger HF

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in training index The training index is based on the user's best results from selected exercises in the program. The Start Index is calculated with the results from days 2 and 3, and the Max Index is calculated with the results from the two best days during the training period. The Index Improvement is calculated by subtracting the Start Index from the Max Index. Changes in training index is measured during 5 weeks of working memory training No
Secondary Neuropsychological testing baseline and 2 months No
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