Cognitive & Motor Training After Stroke For Everyday Walking Restoration

NCT ID: NCT01160653

Last Updated: 2014-02-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2008-08-31

Study Completion Date

2011-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Stroke

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

1

Gait training and Cognitive Training

Group Type EXPERIMENTAL

FES-IM

Intervention Type DEVICE

implantable Functional Electrical Stimulation

Cognitive training

Intervention Type OTHER

training of impaired cognitive processes

2

Able Bodied

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

FES-IM

implantable Functional Electrical Stimulation

Intervention Type DEVICE

Cognitive training

training of impaired cognitive processes

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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)
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

US Department of Veterans Affairs

FED

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Janis Daly, PhD MS

Role: PRINCIPAL_INVESTIGATOR

VA Medical Center-Cleveland

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

VA Medical Center, Cleveland

Cleveland, Ohio, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

UNF1

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Stroke Motor Recovery for the Hand and Fingers
NCT06604143 NOT_YET_RECRUITING NA
Combined Cognitive and Gait Training
NCT02362282 TERMINATED NA
Strength Training and Stroke
NCT00629005 COMPLETED PHASE1/PHASE2