- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05105763
Biofeedback Gait Retraining for Stiff Knee Gait Correction
Biofeedback Gait Retraining for Stiff Knee Gait Correction: Multi-joint Adaptation in Children and Young Adults With Brain Injury
Study Overview
Status
Conditions
Detailed Description
Participant characteristics
This study will recruit 10 participants according to the inclusion and exclusion criteria.
System development
In order to measure the quantitative change in hip joint angle online, an additional sensor will be placed on the pelvis segment (overlying the sacrum between the posterior superior iliac spines) and added to the current feedback system. Totally four sensors will be used, including the sensors on the pelvis, thigh, shank, and heel. The hip flexion angle will be calculated from pelvis and thigh sensors. The knee flexion angle will be calculated from thigh and shank sensors, while the heel sensor signal is monitored to isolate strides by detecting contact of the foot with the support surface. To help subjects easily recognize which joint the feedback is cueing for, different backgrounds is selected for the feedback interface for the hip joint and knee joint, respectively. Gait patterns will be video recorded in a sagittal view of the lower extremities. In order to test gait asymmetry by symmetry ratio (dividing the smaller value by the larger value between trained and untrained lower limbs), stance phase duration (% gait cycle) from heel strike to toe off will be identified by motion capturing system with reflective markers. Reflective markers will be placed on the ankles and shoes (fifth metatarsal, heel, rearfoot along the line from heel to toe and below the ankle) on both sides to measure the heel down and toe off events.
Biofeedback gait retraining protocol
Feedback training on the knee alone (Condition B) will include four 6-mins training blocks: 4-mins knee joint feedback-on and 2-mins feedback-off. Sequential switched feedback training on the knee and the hip (Condition A) will include four 6-mins training blocks: 2-mins knee joint feedback-on, 2-mins hip joint feedback-on, and 2-mins feedback-off. Subjects will wear their comfortable footwear and daily used bracing/orthotic devices during the training sessions. Totally four inertial sensors (MTw, Xsens, Netherlands) will be placed separately on the pelvis, anterior thigh, posterior shank and the heel of the paretic lower limb. For calibration purpose, the subject will first stand in his/her natural standing posture and then stand with the knee (weaker side) flexed at 60 degree adding to the knee angle in the natural standing posture. Prior to training, a treadmill walking trial with comfortable speed will be recorded as the baseline trial. After the baseline trial, a 3 minute practice trial will allow interactive demonstration and practice with the goal that the subject has a clear understanding of the task and how to interpret the feedback. In both the two training conditions, subjects will have 3 mins sitting rest between two consecutive blocks to reduce fatigue.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Xuan Liu, PhD
- Phone Number: 973-324-3561
- Email: XLiu@kesslerfoundation.org
Study Contact Backup
- Name: Peter Barrance, PhD
- Phone Number: 973-324-3550
- Email: pbarrance@kesslerfoundation.org
Study Locations
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New Jersey
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West Orange, New Jersey, United States, 07052
- Recruiting
- Kessler Foundation
-
Contact:
- Xuan Liu, PhD
- Phone Number: 973-324-3561
- Email: XLiu@kesslerfoundation.org
-
Contact:
- Peter Barrance, PhD
- Phone Number: 973-324-3550
- Email: pbarrance@kesslerfoundation.org
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- age 7 to 21;
- has SKG
- diagnosed with brain injury including but not limited to Cerebral Palsy, Stroke,Traumatic Brain Injury;
- ability to walk on a treadmill without assistive devices based on parent/guardian report and/or treatment history;
- the cognitive development is at the level needed to: understand and follow instructions, answer questions, be able to understand the purpose of the study and the activities involved.
Exclusion Criteria:
- Botulinum toxin treatment less than 16 weeks before initiation of the study
- Recent or concurrent treatment that might interfere with the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: feedback training on single joint first
Participants in Subgroup 1 will first undergo Condition B in the first visit and then Condition A in the second visit.
|
Condition A will include four 6-mins training blocks: 2-mins knee joint feedback-on, 2-mins hip joint feedback-on, and 2-mins feedback-off.
Training with feedback on will occur as follows: The subject will walk on the treadmill and try to achieve the target hip and/or knee flexion pattern shown on the feedback interface.
Training with feedback off will occur as follows: The subject will walk on the treadmill and try to maintain the pattern without any form of visual or verbal feedback.
Condition B will include four 6-mins training blocks: 4-mins knee joint feedback-on and 2-mins feedback-off.
Training with feedback on will occur as follows: The subject will walk on the treadmill and try to achieve the target hip and/or knee flexion pattern shown on the feedback interface.
Training with feedback off will occur as follows: The subject will walk on the treadmill and try to maintain the pattern without any form of visual or verbal feedback.
|
|
Other: sequential feedback training on multi-joint first
Participants in Subgroup 2 will start with Condition A in the first visit and then undergo Condition B in the second visit.
|
Condition A will include four 6-mins training blocks: 2-mins knee joint feedback-on, 2-mins hip joint feedback-on, and 2-mins feedback-off.
Training with feedback on will occur as follows: The subject will walk on the treadmill and try to achieve the target hip and/or knee flexion pattern shown on the feedback interface.
Training with feedback off will occur as follows: The subject will walk on the treadmill and try to maintain the pattern without any form of visual or verbal feedback.
Condition B will include four 6-mins training blocks: 4-mins knee joint feedback-on and 2-mins feedback-off.
Training with feedback on will occur as follows: The subject will walk on the treadmill and try to achieve the target hip and/or knee flexion pattern shown on the feedback interface.
Training with feedback off will occur as follows: The subject will walk on the treadmill and try to maintain the pattern without any form of visual or verbal feedback.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Root mean square error of the knee flexion angle
Time Frame: immediate after the first training session
|
The root-mean-square error of the knee flexion angle (RMSE_KF) will be calculated between the measured and target knee flexion angles in the last ten strides of the last trial with feedback off in each training session.
|
immediate after the first training session
|
|
Root mean square error of the knee flexion angle
Time Frame: immediate after the second training session
|
The root-mean-square error of the knee flexion angle (RMSE_KF) will be calculated between the measured and target knee flexion angles in the last ten strides of the last trial with feedback off in each training session.
|
immediate after the second training session
|
|
Peak knee flexion angle
Time Frame: immediate after the first training session
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The Peak knee flexion angle (PKF) is the mean maximum knee flexion angles in the last ten strides of the last trial with feedback off.
|
immediate after the first training session
|
|
Peak knee flexion angle
Time Frame: immediate after the second training session
|
The Peak knee flexion angle (PKF) is the mean maximum knee flexion angles in the last ten strides of the last trial with feedback off.
|
immediate after the second training session
|
|
Peak hip flexion angle
Time Frame: immediate after the first training session
|
The Peak hip flexion angle (PHF) is the mean maximum knee flexion angles in the last ten strides of the last trial with feedback off.
|
immediate after the first training session
|
|
Peak hip flexion angle
Time Frame: immediate after the second training session
|
The Peak hip flexion angle (PHF) is the mean maximum knee flexion angles in the last ten strides of the last trial with feedback off.
|
immediate after the second training session
|
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Minimum relative phase angle between hip and knee
Time Frame: immediate after the first training session
|
Minimum relative phase angle between hip and knee is the minimum difference in phase angle between hip and knee.
Phase angle is computed as the inverse tangent of angular velocity divided by angular displacement.
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immediate after the first training session
|
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Minimum relative phase angle between hip and knee
Time Frame: immediate after the second training session
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Minimum relative phase angle between hip and knee is the minimum difference in phase angle between hip and knee.
Phase angle is computed as the inverse tangent of angular velocity divided by angular displacement.
|
immediate after the second training session
|
|
Symmetry ratio of the stance phase
Time Frame: immediate after the first training session
|
The symmetry ratio is calculated by dividing the smaller value by the larger value (trained vs. untrained lower limbs) of the stance phase time (% gait cycle).
This results in a value between 0.0 and 1.0, with values closer to 1.0 indicating greater symmetry.
|
immediate after the first training session
|
|
Symmetry ratio of the stance phase
Time Frame: immediate after the second training session
|
The symmetry ratio is calculated by dividing the smaller value by the larger value (trained vs. untrained lower limbs) of the stance phase time (% gait cycle).
This results in a value between 0.0 and 1.0, with values closer to 1.0 indicating greater symmetry.
|
immediate after the second training session
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Xuan Liu, PhD, Kessler Foundation
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R-1084-19
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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