Cognitive & Motor Training After Stroke For Everyday Walking Restoration

This study has been terminated.
(The P.I. has moved her lab to Gainesville VA)
Sponsor:
Information provided by (Responsible Party):
Department of Veterans Affairs
ClinicalTrials.gov Identifier:
NCT01160653
First received: April 26, 2010
Last updated: November 21, 2011
Last verified: November 2011

April 26, 2010
November 21, 2011
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 ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01160653 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
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
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: 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.
 
Terminated
10
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)
Both
21 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01160653
UNF1
No
Department of Veterans Affairs
Department of Veterans Affairs
Not Provided
Principal Investigator: Janis Daly, PhD MS VA Medical Center, Cleveland
Department of Veterans Affairs
November 2011

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