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Cognitive & Motor Training After Stroke For Everyday Walking Restoration

This study has been withdrawn prior to enrollment.
(Never funded)
Sponsor:
ClinicalTrials.gov Identifier:
NCT01160653
First Posted: July 12, 2010
Last Update Posted: February 25, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
VA Office of Research and Development
April 26, 2010
July 12, 2010
February 25, 2014
August 2008
August 2011   (Final data collection date for primary outcome measure)
Coordinated Components of gait using the Gait Assessment and Intervention Tool (G.A.I.T.) [ Time Frame: post treatment ]
Same as current
Complete list of historical versions of study NCT01160653 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
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Cognitive & Motor Training After Stroke For Everyday Walking Restoration
Cognitive and Motor Training After Stroke for Everyday Walking Restoration
The purpose of this study is to test a unique, combined cognitive and motor intervention designed to restore safe, more normal coordinated gait components into the real world environment for individuals with stroke.
Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Stroke
  • Device: FES-IM
    implantable Functional Electrical Stimulation
  • Other: Cognitive training
    training of impaired cognitive processes
  • Experimental: 1
    Gait training and Cognitive Training
    Interventions:
    • Device: FES-IM
    • Other: Cognitive training
  • No Intervention: 2
    Able Bodied
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
0
August 2011
August 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • greater than or equal to 6 months post stroke
  • ability to give informed consent
  • impaired gait
  • medically stable

Exclusion Criteria:

  • pacemaker
  • unstable/uncontrolled medical condition(s)
Sexes Eligible for Study: All
21 Years and older   (Adult, Senior)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01160653
UNF1
No
Not Provided
Not Provided
VA Office of Research and Development
VA Office of Research and Development
Not Provided
Principal Investigator: Janis Daly, PhD MS VA Medical Center, Cleveland
VA Office of Research and Development
February 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP