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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02256007
Other study ID # Pro00031722
Secondary ID
Status Terminated
Phase N/A
First received September 28, 2014
Last updated April 3, 2018
Start date September 2014
Est. completion date July 2015

Study information

Verified date April 2018
Source Cedars-Sinai Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study designs and develops an evidence-based game approach that will enhance the investigators understanding and usability of electronic tools to measure cognitive and sensorimotor abilities in an inpatient rehabilitation stroke population.


Description:

The rehabilitation industry is the incipient stages of developing and using electronic based assessment and intervention tools. With the growing understanding of cognitive recovery following stroke, rehabilitation specialists are optimistic that appropriate rehabilitation interventions may optimize and enhance functional outcomes. The use of technology based assessments via video games may assist in a patient's cognitive recovery. Design and development of an evidence-based game approach will enhance the investigators understanding and usability of electronic tools to measure cognitive and sensorimotor abilities. There is no intervention only an assessment for usability.


Recruitment information / eligibility

Status Terminated
Enrollment 2
Est. completion date July 2015
Est. primary completion date July 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- New onset stroke

- Ability to follow one-step commands

- All participants must be admitted to the inpatient rehabilitation unit at Cedars-Sinai Medical Center

- Scores needed for Participation in Study on the Complex Ideational Material-Short Form from the Boston Diagnostic Aphasia Examination and the Montreal Cognitive Assessment:

- Complex Ideational Material-Short Form from the Boston Diagnostic Aphasia Examination-Participants must obtain a total score of at least 5/6 item pairs to participate

- Montreal Cognitive Assessment-Participants must obtain a total score of 16 or greater and obtain a score of 6/6 on the orientation subtest

- In order to participate, participants must meet both of the above criteria

Exclusion Criteria:

- Patients who do not meet inclusion criteria as noted above.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Paper and Pencil Assessments
Videogame Assessments

Locations

Country Name City State
United States Pamela Roberts Los Angeles California

Sponsors (2)

Lead Sponsor Collaborator
Cedars-Sinai Medical Center Blue Marble Rehab Inc

Country where clinical trial is conducted

United States, 

References & Publications (3)

King M, Hale L, Pekkari A, Persson M, Gregorsson M, Nilsson M. An affordable, computerised, table-based exercise system for stroke survivors. Disabil Rehabil Assist Technol. 2010 Jul;5(4):288-93. doi: 10.3109/17483101003718161. — View Citation

Lewis GN, Rosie JA. Virtual reality games for movement rehabilitation in neurological conditions: how do we meet the needs and expectations of the users? Disabil Rehabil. 2012;34(22):1880-6. Epub 2012 Apr 5. Review. — View Citation

Lewis GN, Woods C, Rosie JA, McPherson KM. Virtual reality games for rehabilitation of people with stroke: perspectives from the users. Disabil Rehabil Assist Technol. 2011;6(5):453-63. doi: 10.3109/17483107.2011.574310. Epub 2011 Apr 17. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Usability Questionnaire Participant will perform videogame assessments and standardized paper-pencil assessments and evaluate the utility of the touch screen tests compared to the traditional testing methods using the Usability Questionnaire. The focus will be on the Usability Questionnaire (not the video or paper assessments) Session in which participant completes standardized assessments before the patient's discharge from inpatient rehabilitation (within 2 weeks)
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