Dual Joint Visual Feedback Gait Retraining in Pediatric Hemiplegic Cerebral Palsy
Primary Purpose
Hemiplegic Cerebral Palsy
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Dual Joint Visual Feedback without Scoring
Dual Joint Visual Feedback with Scoring
Sponsored by
About this trial
This is an interventional device feasibility trial for Hemiplegic Cerebral Palsy focused on measuring gait, biofeedback
Eligibility Criteria
Inclusion Criteria:
- I1: Diagnosis of hemiplegic cerebral palsy
- I2: Gait pattern in hemiplegic limb: deficit of knee extension during late swing phase/initial contact
- I3: Age 7 to 17 years
- I4: Able to walk on a treadmill without assistive devices
I5: Able to understand spoken English at the level needed to:
- understand and follow instructions for equipment setup, testing and task performance
- answer questions related to effort and preference
- be able to understand consent document and provide informed consent
Exclusion Criteria:
- E1: Significant injury (such as fracture) in legs or feet that interferes with their ability to walk
- E2: Known risk factor for stroke or heart attack while exercising
- E3: Lower extremity orthopaedic surgery less than 12 months prior to study start
- E4: Other significant health conditions that may interfere with the participant's ability to complete the study or could interfere with interpretation of the study results.
Sites / Locations
- Kessler FoundationRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Experimental Group
Arm Description
Participants will undergo a single testing session of gait retraining using two variants of the dual joint visual feedback system (DJVF). The DJVF system uses IMU sensors to measure knee and hip joint motions and calculates the users foot position, relative to their pelvis. The relative foot position is represented in real time on a screen in front of the user with feedback designed to elicit increases in anteriorly located foot positions.
Outcomes
Primary Outcome Measures
Knee flexion angle at initial contact without feedback
Measurement of how bent the knee is when the foot touches the ground at the end of the swing phase without feedback
Knee flexion angle at initial contact during FBC exposure
Measurement of how bent the knee is when the foot touches the ground at the end of the swing phase during exposure to FBC visual feedback
Knee flexion angle at initial contact during FBCS exposure
Measurement of how bent the knee is when the foot touches the ground at the end of the swing phase during exposure to FBCS visual feedback
Hip flexion angle at initial contact without feedback
Measurement of how flexed the hip is when the foot touches the ground at the end of the swing phase without feedback
Hip flexion angle at initial contact during FBC exposure
Measurement of how flexed the hip is when the foot touches the ground at the end of the swing phase during exposure to FBC visual feedback
Hip flexion angle at initial contact during FBCS exposure
Measurement of how flexed the hip is when the foot touches the ground at the end of the swing phase during exposure to FBCS visual feedback
Participant questionnaire responses
Participant responses to a five-point ordinal scale detailing their 1) comprehension of the feedback display, 2) self-rating of success, 3) preference of which feedback variant (intervention) they preferred, and 4) effort or exhaustion following training.
Secondary Outcome Measures
Full Information
NCT ID
NCT05011201
First Posted
July 27, 2021
Last Updated
January 14, 2022
Sponsor
Kessler Foundation
Collaborators
Children's Specialized Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05011201
Brief Title
Dual Joint Visual Feedback Gait Retraining in Pediatric Hemiplegic Cerebral Palsy
Official Title
Impact and Feasibility of a Dual Joint Visual Feedback Design in Pediatrics With Hemiplegic Cerebral Palsy: A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 19, 2021 (Actual)
Primary Completion Date
May 2022 (Anticipated)
Study Completion Date
August 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
This study aims to assess the feasibility of a visual feedback system designed to augment treadmill-based gait training for children with gait disturbances related to hemiplegic cerebral palsy. The visual feedback uses data from knee and hip joint movements to represent the position of the foot ahead of or behind the body during walking. This study will test eight children with hemiplegic cerebral palsy who have short step lengths related to atypical knee and hip motions when the foot contacts the ground (initial contact). The study will examine walking adaptations in response to the new visual feedback system and compare differences in response and user experience between two variants of the new design. In a single visit, participants will undergo a gait retraining protocol using the dual joint visual feedback (DJVF) system. Hip and knee flexion angles of the paretic (weaker) side will be collected, analyzed, and compared during baseline walking and while responding to the two feedback variants. Muscle firing patterns will be studied using electrodes placed on key lower limb muscles. Study participants will be asked to report their experience and preferences following the gait retraining protocol. The study findings will be used to further refine the DJVF system in preparation for future studies.
Detailed Description
Participant characteristics
This study will recruit 8 pediatric participants with hemiplegic gait secondary to CP, in accordance with the inclusion and exclusion criteria.
Dual Joint Visual Feedback System (DJVF)
The DJVF system uses four inertial measurement unit (IMU) sensors (MTW Devkit, Xsens Technologies BV, Enschede, Netherlands) which are placed on the pelvis, shank, thigh, and foot, to measure three-dimensional segment accelerations and orientations during gait. The software application has been developed by our study team using the MATLAB (Mathworks, Natick, MA) programming language and the application programming interface supplied with the Xsens system. Sensor data is relayed back to a controlling PC for processing and feedback display formulation in real-time. The primary feedback is in the form of a cursor representing the position of the foot ahead of or behind the body. Relative foot position is calculated using the segmental angle and lengths of the paretic thigh and shank. The feedback is designed to reward a more anterior foot placement at the initial contact phase of gait by awarding points according to target screen zones that the cursor enters. The zone reached is highlighted and the instantaneous score is displayed.
FBC vs FBCS: addition of cumulative scoring:
Two feedback conditions representing two variants will be tested. The first (FBC) is as above, with only instantaneous scoring. The FBCS condition will be the same as the FBC condition with the following addition: game context cues of the cumulative score will be provided as visual numerical count displayed to the right of the main feedback interface.
Study Protocol
Researchers will place inertial sensors on the pelvis, thigh, shank, and shoe of the paretic limb, using elastic wraps and medical tape. Researchers will place surface EMG sensors on the participant's lower extremity paretic side. If any sensors cannot be placed due to the presence of orthotics or other complicating factors, data for that sensor will not be collected. Researchers will check the signal of each sensor, by having participants perform some easy activities such as flexing their knee, squatting, going on their toes, and raising their toes.
Following setup, participants will first walk on the study treadmill at a self-selected comfortable speed while baseline (BAS) gait patterns are recorded. After the baseline trial, practice, and orientation to the feedback, including the FBC and FBCS variants, will occur. The order of these training blocks will be randomized prior to participant arrival. Between training blocks, participants will be allotted rest periods to reduce fatigue.
Following testing, participants will complete a questionnaire with items on a five-point ordinal scale describing their 1) comprehension of the feedback display, 2) self-rating of success, 3) preference of which feedback variant (intervention) they preferred, and 4) effort or exhaustion following training.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemiplegic Cerebral Palsy
Keywords
gait, biofeedback
7. Study Design
Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All participants will take part in the same interventional model. Participants will undergo several gait retraining bouts using two variants of the DJVF system. The order of bouts during the gait retraining will be block randomized.
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental Group
Arm Type
Experimental
Arm Description
Participants will undergo a single testing session of gait retraining using two variants of the dual joint visual feedback system (DJVF). The DJVF system uses IMU sensors to measure knee and hip joint motions and calculates the users foot position, relative to their pelvis. The relative foot position is represented in real time on a screen in front of the user with feedback designed to elicit increases in anteriorly located foot positions.
Intervention Type
Device
Intervention Name(s)
Dual Joint Visual Feedback without Scoring
Intervention Description
Participants will walk on the treadmill while given instantaneous anterior and posterior foot position and immediate scoring information using the DJVF interface. A pediatric physical therapist will provide (1) verbal encouragement and redirection of attention to the task as needed (2) verbal cueing to assist if difficulty in interpreting the feedback and appropriate modification is noted.
Intervention Type
Device
Intervention Name(s)
Dual Joint Visual Feedback with Scoring
Intervention Description
Participants will walk on the treadmill using the same DJFB with additional visual cumulative scoring on their performance. A pediatric physical therapist will provide (1) verbal encouragement and redirection of attention to the task as needed (2) verbal cueing to assist if difficulty in interpreting the feedback and appropriate modification is noted.
Primary Outcome Measure Information:
Title
Knee flexion angle at initial contact without feedback
Description
Measurement of how bent the knee is when the foot touches the ground at the end of the swing phase without feedback
Time Frame
1 day (At single time point)
Title
Knee flexion angle at initial contact during FBC exposure
Description
Measurement of how bent the knee is when the foot touches the ground at the end of the swing phase during exposure to FBC visual feedback
Time Frame
1 day (At single time point)
Title
Knee flexion angle at initial contact during FBCS exposure
Description
Measurement of how bent the knee is when the foot touches the ground at the end of the swing phase during exposure to FBCS visual feedback
Time Frame
1 day (At single time point)
Title
Hip flexion angle at initial contact without feedback
Description
Measurement of how flexed the hip is when the foot touches the ground at the end of the swing phase without feedback
Time Frame
1 day (At single time point)
Title
Hip flexion angle at initial contact during FBC exposure
Description
Measurement of how flexed the hip is when the foot touches the ground at the end of the swing phase during exposure to FBC visual feedback
Time Frame
1 day (At single time point)
Title
Hip flexion angle at initial contact during FBCS exposure
Description
Measurement of how flexed the hip is when the foot touches the ground at the end of the swing phase during exposure to FBCS visual feedback
Time Frame
1 day (At single time point)
Title
Participant questionnaire responses
Description
Participant responses to a five-point ordinal scale detailing their 1) comprehension of the feedback display, 2) self-rating of success, 3) preference of which feedback variant (intervention) they preferred, and 4) effort or exhaustion following training.
Time Frame
1 day (At single time point)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
I1: Diagnosis of hemiplegic cerebral palsy
I2: Gait pattern in hemiplegic limb: deficit of knee extension during late swing phase/initial contact
I3: Age 7 to 17 years
I4: Able to walk on a treadmill without assistive devices
I5: Able to understand spoken English at the level needed to:
understand and follow instructions for equipment setup, testing and task performance
answer questions related to effort and preference
be able to understand consent document and provide informed consent
Exclusion Criteria:
E1: Significant injury (such as fracture) in legs or feet that interferes with their ability to walk
E2: Known risk factor for stroke or heart attack while exercising
E3: Lower extremity orthopaedic surgery less than 12 months prior to study start
E4: Other significant health conditions that may interfere with the participant's ability to complete the study or could interfere with interpretation of the study results.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Peter J Barrance, PhD
Phone
9733243550
Email
pbarrance@kesslerfoundation.org
First Name & Middle Initial & Last Name or Official Title & Degree
Erik Hummer, PhD
Phone
973 965 6624
Email
ehummer@kesslerfoundation.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter J Barrance, 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
Peter J Barrance, PhD
Phone
973-324-3550
Email
PBarrance@KesslerFoundation.org
First Name & Middle Initial & Last Name & Degree
Peter J Barrance, PhD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Dual Joint Visual Feedback Gait Retraining in Pediatric Hemiplegic Cerebral Palsy
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