MedDataX Logo

Innovative Modalities for Restoring Upper Limb Function Post Stroke

NCT ID: NCT01725659

Last Updated: 2012-11-14

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

COMPLETED

Clinical Phase

NA

Total Enrollment

35 participants

Study Classification

INTERVENTIONAL

Study Start Date

2001-09-30

Study Completion Date

2009-12-31

Brief Summary

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

PURPOSE. After stroke many patients are unable to engage in normal upper limb functional activities, which may restrict them from participation in meaningful life roles. For many, conventional rehabilitation does not restore upper limb function to a useful level. The purpose of this research is to investigate the benefits of three promising motor learning interventions: focused intensive, motor learning (FIML); 2) robotics and motor learning (ROB-ML); and 3) functional neuromuscular stimulation and motor learning (FNS-ML).

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.

Cerebrovascular Accident

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Stroke electric stimulation robotics motor learning

Study Design

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

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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.

Motor Learning

subjects are provided with intensive motor learning training of the upper limb

Group Type EXPERIMENTAL

Motor Learning

Intervention Type OTHER

training of the hemiplegic upper limb with motor learning

Robotics and Motor Learning

subject are provided with intensive motor learning and robotics training of the upper limb

Group Type EXPERIMENTAL

Motor Learning

Intervention Type OTHER

training of the hemiplegic upper limb with motor learning

Robotics

Intervention Type OTHER

subjects perform training of hemiplegic arm using an upper extremity robot

Motor learning and FES

subjects are provided with intensive motor learning and surface FES (Functional Electrical Stimulation) of the upper limb

Group Type EXPERIMENTAL

Motor Learning

Intervention Type OTHER

training of the hemiplegic upper limb with motor learning

surface FES

Intervention Type OTHER

subjects are provided with surface FES to the hemiplegic upper limb

Interventions

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

Motor Learning

training of the hemiplegic upper limb with motor learning

Intervention Type OTHER

Robotics

subjects perform training of hemiplegic arm using an upper extremity robot

Intervention Type OTHER

surface FES

subjects are provided with surface FES to the hemiplegic upper limb

Intervention Type OTHER

Eligibility Criteria

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

Inclusion Criteria

* \>1 year post stroke no acute, uncontrolled medical condition single stroke

Exclusion Criteria

* pacemaker other neurological condition more than one stroke
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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

Malcom Randall VA Medical Center

FED

Sponsor Role lead

Responsible Party

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

Janis Daly

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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

Louis Stokes Cleveland Department of Veterans Affairs Medical Center

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.

B2801R

Identifier Type: -

Identifier Source: org_study_id