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Walking Therapy In Hemiparetic Stroke Patients Using Robotic-Assisted Treadmill Training

Gait Restoration In Hemiparetic Stroke Patients Using Goal-Directed, Robotic-Assisted, Treadmill Training

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00075283
Enrollment
50
Registered
2004-01-09
Start date
2002-11-30
Completion date
Unknown
Last updated
2005-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemiparesis, Stroke

Keywords

Physical Therapy, Locomotion therapy, Gait training, Stroke, Robotics, Rehabilitation, Treadmill, Hemiparetic stroke, Unilateral brain lesion

Brief summary

The overall goal of this study is to determine whether robotic-assisted gait training is better than standard physical therapy treatments for improving walking ability in hemiparetic stroke patients.

Detailed description

Subjects enrolled into the study will be randomly assigned to one of 2 groups. The first group will receive one hour of conventional gait training, consisting of lower extremity strengthening exercises, stretching, and full weight bearing walking as tolerated, with appropriate physical assistance from a therapist. The second group will receive walking therapy using a Lokomat, which is a special treadmill that works in conjunction with 2 light-weight robotic arms that assists the subject to move their legs while they try to walk on the treadmill. Some of the subject's body-weight will be supported using a harness. During Lokomat training sessions, subjects will receive feedback of their walking performance on a computer monitor to help them walk. Both groups will be trained for 8-10 weeks, 3 times per week, for 1 hour training sessions (24 total sessions). Resources for transportation to the National Rehabilitation Hospital will be provided to all study participants.

Interventions

DEVICELokomat (Robotic Orthosis) combined with slat belt treadmill

Sponsors

U.S. Department of Education
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Inclusion: * Unilateral brain lesion. * Within 6 months post-stroke. * Receiving no other therapy targeting function of lower limb. * Demonstration of hemiparesis (motor dysfunction in lower limb). * Able to walk 5 meters without therapist assistance (walking device only). * Able to follow commands and protocol. Exclusion: * Significant cognitive or communication impairments. * Uncontrolled hypertension. * Uncontrolled diabetes. * Clinical depression.

Countries

United States

Contacts

Primary ContactCheryl M Lacsamana, BBE
cheryl.lacsamana@medstar.net(202)877-1889

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026