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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01684267
Other study ID # 2009-P-000447
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date January 2012
Est. completion date May 2016

Study information

Verified date April 2019
Source Spaulding Rehabilitation Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To test the usability and effectiveness of a robotic device, called the Robotic Gait Rehabilitation (RGR) Trainer, in (1) healthy subjects with no gait impairment and (2) patients with stroke with gait abnormalities secondary to impaired knee function.


Description:

The device is designed to train stroke patients to correct abnormal gait patterns associated with exaggerated and uncoordinated movements of the pelvis by applying force fields to correct the movement of the pelvis. The focus will be on correcting hip hiking (i.e. exaggerated unilateral upward movements of one side of the pelvis) in post-stroke patients. The human-robot interface will be based on impedance control techniques so that the force-field actuators generate smooth virtual spring/damper restitution forces at the patient's pelvic area.

As part of the study we will determine whether the force fields applied by the actuated components of the device can effect an acute change in gait biomechanics, primarily pelvis motion during stance and swing phases, in healthy subjects and patients with stroke during ambulation. The investigators will also evaluate the usability of the orthosis in terms of donning & doffing, user confidence, and comfort.


Recruitment information / eligibility

Status Terminated
Enrollment 23
Est. completion date May 2016
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 70 Years
Eligibility HEALTHY

Inclusion Criteria:

- Can walk comfortably on a treadmill

Exclusion Criteria:

- any known orthopedic, musculoskeletal, neurological, cardiovascular, pulmonary, or gait disorder that results in an abnormal gait pattern

- Females in the second or third trimester of pregnancy

STROKE

Inclusion Criteria:

- single non-traumatic ischemic or hemorrhagic stroke at least 6 months prior to enrollment

- persistent hemiparesis, mild spasticity, and residual mild-to-moderate weakness of the lower extremity

- residual deficits of gait

- be able to ambulate without the use of assistive devices or assistance of a person

- able to walk at a comfortable walking speed of ~0.6 m/s

- able to walk safely on a treadmill

- medically stable

- No other neurological problems, or any known cardiovascular or musculoskeletal disorders that effects their gait or excludes them from exercise

Exclusion Criteria:

- unable to attend and follow instructions

- require physical assistance for ambulation

- other known orthopedic, musculoskeletal, neurological, cardiovascular, pulmonary, or gait disorder that results in an abnormal gait pattern

- severe joint contractures of the hemi-paretic knee

- females in the second or third trimester of pregnancy

Study Design


Related Conditions & MeSH terms

  • Gait Re-training in Healthy Subjects
  • Gait Re-training in Stroke Survivors
  • Stroke

Intervention

Device:
Robotic Gait Rehabilitation (RGR) Trainer


Locations

Country Name City State
United States Spaulding Rehabilitation Hospital Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Spaulding Rehabilitation Hospital Northeastern University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pelvic obliquity Change in pelvic obliquity during gait consequent to force application 1 day