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Interactive Exoskeleton Robot for Walking - Knee Joint

Interactive Exoskeleton Robot for Walking - Knee Joint

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02497703
Enrollment
25
Registered
2015-07-14
Start date
2015-05-27
Completion date
2016-12-31
Last updated
2017-09-18

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

Conditions

Stroke

Brief summary

An exoskeleton robotic knee system for stroke rehabilitation is proposed in this study. This robotic system has been developed to facilitate functional motor recovery by practices walking with a one joint motor powered exoskeleton to reduce the muscle weakness in the shank and reduce the hyperextension in the knee joint. The robotic knee system is able to sense the gait pattern from the stroke patients and assist the walking and control the knee angle. The clinical trial will use repeated measurements to evaluate the effectiveness of the robotic knee system in gait rehabilitation post stroke.

Interventions

DEVICEKnee robot

Sponsors

The Hong Kong Polytechnic University
CollaboratorOTHER
Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. Ischemic or hemorrphagic stroke with drop foot problem. 2. Sufficient cognition to follow simple instructions and to understand the content and purpose of the study. (Mini-Mental State Examination \> 20) 3. Capable of standing and walking independently for an extended period of time. (Functional Ambulation Category \> 3, Berg Balance Scale \> 40)

Exclusion criteria

1. Any medical or psychological dysfunctions that would affect their ability to comply with test study protocol, such as lower back pain, neuralgia, rotational vertigo, muscloskeletal disorders, injuries, and pregnancy. 2. Any severe contractures in hip, knee, or ankle joint that would preclude passive range of motion in the lower extremity. 3. Participation in any therapeutic treatment (outside therapy) performed with the lower extremity during the planned study, including the baseline and the followup.

Design outcomes

Primary

MeasureTime frameDescription
Functional Ambulation Category3-month followupPatients can be rated on the following categories: 0: Patient cannot walk, or needs help from 2 or more persons 1. Patients needs firm continuous support from 1 person who helps carrying weight and with balance 2. Patient needs continuous or intermittent support of one person to help with balance and coordination. 3. Patient requires verbal supervision or stand-by help from one person without physical contact 4. Patient can walk independently on level ground, but requires help on stairs, slopes or uneven surfaces 5. Patient can walk independently anywhere
6-minute Walk Test3-month followupWalk as far a distance as possible over 6 minutes with their preferred speed; assistive devices can be used but kept consistent from test to test Individual should be able to ambulate without physical assistance.

Secondary

MeasureTime frameDescription
Timed 10-meter Walk Test3-month followupThe individual is instructed to walk a set distance (10 meters). Time is measured while the individual walks the set distance (often the individual is given space to accelerate to his/her preferred walking speed (this distance is not included when determining speed). The distance covered is divided by the time it took the individual to walk that distance.
Kinematic and Kinetic Gait Motion Capture3-month followupMotion analysis to evaluation the ankle, knee and hip angles; and ground reaction force
Berg Balance Scale3-month followupStatic and dynamic activities of varying difficulty are performed Item-level scores range from 0-4, determined by ability to perform the assessed activity Item scores are summed Maximum score = 56
Modified Ashworth Scale3-month followupTests resistance to passive movement about a joint with varying degrees of velocity; scores range from 0-4, with 6 choices
Fugl-Meyer Assessment Lower Extremity3-month followupEvaluates and measures motor function recovery in post-stroke hemiplegic patients Used in both clinical and research settings, maximum score = 34

Countries

Hong Kong

Outcome results

None listed

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