Biofeedback Gait Retraining for Stiff Knee Gait Correction
Primary Purpose
Brain Injury
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sequential switched feedback training on the knee and the hip (Condition A)
Feedback training on the knee alone (Condition B)
Sponsored by
About this trial
This is an interventional other trial for Brain Injury focused on measuring stiff knee gait, biofeedback
Eligibility Criteria
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.
Sites / Locations
- Kessler FoundationRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
feedback training on single joint first
sequential feedback training on multi-joint first
Arm Description
Participants in Subgroup 1 will first undergo Condition B in the first visit and then Condition A in the second visit.
Participants in Subgroup 2 will start with Condition A in the first visit and then undergo Condition B in the second visit.
Outcomes
Primary Outcome Measures
Root mean square error of the knee flexion angle
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.
Root mean square error of the knee flexion angle
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.
Peak knee flexion angle
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.
Peak knee flexion angle
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.
Peak hip flexion angle
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.
Peak hip flexion angle
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.
Minimum relative phase angle between hip and knee
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.
Minimum relative phase angle between hip and knee
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.
Symmetry ratio of the stance phase
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.
Symmetry ratio of the stance phase
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.
Secondary Outcome Measures
Full Information
NCT ID
NCT05105763
First Posted
September 29, 2021
Last Updated
March 30, 2022
Sponsor
Kessler Foundation
Collaborators
Children's Specialized Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05105763
Brief Title
Biofeedback Gait Retraining for Stiff Knee Gait Correction
Official Title
Biofeedback Gait Retraining for Stiff Knee Gait Correction: Multi-joint Adaptation in Children and Young Adults With Brain Injury
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 30, 2021 (Actual)
Primary Completion Date
June 30, 2022 (Anticipated)
Study Completion Date
September 29, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kessler Foundation
Collaborators
Children's Specialized Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The research team has developed a visual kinematic biofeedback system which is designed to help children with hemiplegic cerebral palsy (CP) correct a pattern of reduced knee extension in terminal swing and early stance. The system provides real-time feedback on the knee angle pattern during walking on a treadmill. From a pilot study on children with CP, the investigators observed that when the system was used in children who have stiff knee gait (SKG), training with knee feedback alone could lead to an increase in hip flexion which in turn led to limited normalization of the knee pattern through the whole gait cycle. This study, funded by the NIDILRR Switzer grant (PI: X Liu, Ph.D.), seeks to address the question of whether a training design with feedback on both the knee and hip joints would reduce this tendency to generate unintended changes in hip joint motion, and in doing so also improve convergence to the intended knee joint pattern. This study will test ten children and young adults with brain injury who have SKG and examine their short term adaptations to two types of kinematic feedback training: feedback training on the knee alone (condition B) and sequential switched feedback training on the knee and the hip (condition A). An additional sensor placed on the pelvis will be added to the current feedback system for measurement and feedback on the hip joint angle. Software enhancements will also be made with methods that will allow study and description of adaptations in measures of inter-limb symmetry during training. The participants will visit twice with a 2-week washout period between the two visits. Five participants will first undergo condition B in the first visit and then condition A in the second visit, while the other five participants will start with condition A in the first visit and then undergo condition B in the second visit. To compare the effects of the conditions on normalizing the joint angle trajectories, the knee and hip kinematics will be collected and analyzed in both the conditions. To investigate the coordination of lower limb segments under feedback training, relative phase measures will be analyzed on the hip and the knee. To examine whether participants adapt to the feedback retraining in terms of improvement in gait quality, symmetry ratios will be analyzed.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Injury
Keywords
stiff knee gait, biofeedback
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
A counterbalanced repeated measures design will be used in this study to examine the adaptation of children and young adults with brain injury who have SKG to two types of feedback training: feedback training on the knee alone (Condition B) and sequential switched feedback training on the knee and the hip (Condition A). The participants will participate in treadmill training twice with a 2-weeks washout period between the two visits and will receive the two training conditions in different orders. Ten participants will be alternately allocated to two subgroups according to the sequence they are recruited to the study. In the end, the investigators will have five participants in Subgroup 1 and the other five participants in Subgroup 2. Participants in Subgroup 1 will first undergo Condition B in the first visit and then Condition A in the second visit, while participants in Subgroup 2 will start with Condition A in the first visit and then undergo Condition B in the second visit.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
feedback training on single joint first
Arm Type
Other
Arm Description
Participants in Subgroup 1 will first undergo Condition B in the first visit and then Condition A in the second visit.
Arm Title
sequential feedback training on multi-joint first
Arm Type
Other
Arm Description
Participants in Subgroup 2 will start with Condition A in the first visit and then undergo Condition B in the second visit.
Intervention Type
Other
Intervention Name(s)
Sequential switched feedback training on the knee and the hip (Condition A)
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Feedback training on the knee alone (Condition B)
Intervention Description
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.
Primary Outcome Measure Information:
Title
Root mean square error of the knee flexion angle
Description
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.
Time Frame
immediate after the first training session
Title
Root mean square error of the knee flexion angle
Description
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.
Time Frame
immediate after the second training session
Title
Peak knee flexion angle
Description
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.
Time Frame
immediate after the first training session
Title
Peak knee flexion angle
Description
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.
Time Frame
immediate after the second training session
Title
Peak hip flexion angle
Description
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.
Time Frame
immediate after the first training session
Title
Peak hip flexion angle
Description
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.
Time Frame
immediate after the second training session
Title
Minimum relative phase angle between hip and knee
Description
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.
Time Frame
immediate after the first training session
Title
Minimum relative phase angle between hip and knee
Description
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.
Time Frame
immediate after the second training session
Title
Symmetry ratio of the stance phase
Description
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.
Time Frame
immediate after the first training session
Title
Symmetry ratio of the stance phase
Description
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.
Time Frame
immediate after the second training session
10. Eligibility
Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xuan Liu, PhD
Phone
973-324-3561
Email
XLiu@kesslerfoundation.org
First Name & Middle Initial & Last Name or Official Title & Degree
Peter Barrance, PhD
Phone
973-324-3550
Email
PBarrance@kesslerfoundation.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xuan Liu, PhD
Organizational Affiliation
Kessler Foundation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kessler Foundation
City
West Orange
State/Province
New Jersey
ZIP/Postal Code
07052
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xuan Liu, PhD
Phone
973-324-3561
Email
XLiu@kesslerfoundation.org
First Name & Middle Initial & Last Name & Degree
Peter Barrance, PhD
Phone
973-324-3550
Email
PBarrance@kesslerfoundation.org
12. IPD Sharing Statement
Plan to Share IPD
No
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Biofeedback Gait Retraining for Stiff Knee Gait Correction
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