search
Back to results

Step Rate Retraining to Reduce Injury and Disability (STRIDe) (STRIDe)

Primary Purpose

Overuse Injury, Lower Extremity Problem, Stress Injury, Repetitive

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Run Gait Retraining
Sponsored by
Army-Baylor University Doctoral Program in Physical Therapy
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Overuse Injury focused on measuring Running-related lower extremity overuse injuries

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Between the age of 18 - 50 years
  • Active Duty, Department of Defense beneficiaries
  • History of running-related overuse, musculoskeletal injury of the lower extremity (knee, hip, lower leg, or bone stress injury) within the last six months
  • Currently able to run continuously for at least 15 minutes at self-selected pace, 3 times per week.
  • Read and speak English well enough to provide informed consent and follow study instructions

Exclusion Criteria:

  • Known pregnancy currently or in the previous 6 months
  • Lower extremity or low back surgery in the previous 6 months
  • Any lower extremity or low back exercise profile that limits running
  • Participant has already completed a step rate, gait retraining program
  • Participant has a step rate greater than 176 steps per minute

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Retraining (RT) Group

    Control (CON) Group

    Arm Description

    The retraining group will receive a watch accelerometer to use for monitoring their step rate with instructions to increase their preferred step rate by 7.5% over the ten in-field training sessions.

    The control group will receive the same device to monitor their pace but receive no instruction to change their preferred step rate over the ten in-field training sessions.

    Outcomes

    Primary Outcome Measures

    Change in Average vertical loading rate (AVLR)
    The slope of the line on a ground reaction force curve from initial contact to the impact peak
    Change in Step rate (SR)
    The number of steps a participant takes per minute of running
    Injury
    The number of lower extremity, over-use injuries sustained within 1 year after completing the ten in-field training sessions

    Secondary Outcome Measures

    Absolute risk reduction
    Change in risk for lower extremity, over-use injuries in those that complete step rate retraining
    Limited duty days
    Number of days a soldier is non-deployable due to a lower extremity, over-use injury

    Full Information

    First Posted
    July 24, 2020
    Last Updated
    February 8, 2021
    Sponsor
    Army-Baylor University Doctoral Program in Physical Therapy
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT04747223
    Brief Title
    Step Rate Retraining to Reduce Injury and Disability (STRIDe)
    Acronym
    STRIDe
    Official Title
    Step Rate Retraining to Reduce Injury and Disability: A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    February 1, 2021 (Anticipated)
    Primary Completion Date
    June 1, 2022 (Anticipated)
    Study Completion Date
    December 31, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Army-Baylor University Doctoral Program in Physical Therapy

    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 will be the first project to evaluate the effectiveness of wearable technology (Garmin Forerunner35) while performing gait retraining in field on military members. The watch will provide real time feedback to the runner on their step rate while performing running sessions outside of the lab. This allows the runner to modify their step rate to meet a recommended step rate provided by the study team member. Aim 1: To demonstrate the utility of wearable sensors to modify running step rate through real time biofeedback. Aim 2: To determine whether altering step rate using real time biofeedback reduces lower extremity musculoskeletal injury reoccurrence within 1 year post training.
    Detailed Description
    Volunteers meeting all inclusion and exclusion criteria will read and sign an informed consent form approved by the institutional review board (IRB). After consenting, each participant will answer a demographic questionnaire related to injury history and pertinent injury risk factors (location, duration and type of previous injury, profile time, height, weight, changes in menstruation, etc). The participant will then undergo a running analysis in which the individual will run on an instrumented treadmill while video of running form in the sagittal plane and frontal plane are captured using two stationary two-dimensional digital cameras sampling at 240 Hz. The video will capture the runner from the waist down in order to protect privacy and blinding. Information collected from the treadmill will include AVLR of vGRF, while step rate and other kinematic information will be collected from video analysis. Volunteers will run at their self-selected pace for three minutes on a treadmill, with step rate and AVLR analyzed during the last minute of running. During the inital data collection, if the participant's step rate is greater than 176 spm, the participant will be exluded from the study at this time. The same data collection procedure will be repeated for all participants after retraining and for a subset of participants at 6 months to observe post intervention AVLR and step rate. Volunteers will then be placed into a retraining group and a control group through random allocation. Each participant, regardless of group, will be provided a Garmin Forerunner35 to use while performing PRT with their unit and/or personal physical training for ten in-field training sessions. The ten in-field training sessions will be performed by the participant outside of the researcher's lab without a researcher present. The participant will be instructed to return to their normal running routine, but to use the watch during 10 running sessions to either monitor and modify their step rate for the retraining group or their pace and distance for the control group. Both groups will receive a training log to track their training sessions. The retraining group will receive a watch accelerometer to use for monitoring their step rate with instructions to increase their preferred step rate by 7.5% over the ten in-field training sessions. The runner will receive a training log with a target step rate recorded on it. The target step rate will be a 7.5% increase from the preferred step rate the runner used during the gait analysis. The researcher will provide instruction to the participant to match the target step rate while the participants are performing their in-field training sessions by using the watch to monitor their step rate. The watch provides the runner with real-time feedback on their step rate. This allows the runner to monitor their step rate while running and the runner should either increase or decrease their step rate to meet the target step rate provided by the study team member. Training units at FT. Sam Houston perform ability group or self-paced runs for the majority of their endurance training, so participants should not have difficulty adjusting their step rates IAW study plans. Willy et al. was successful using eight in-field training sessions to sustain a 7.5% increase in step rate 1 month post-training in healthy runners (Willy 2016). Adherence to step rate will be assessed at the follow-up by reviewing the last 7 training sessions in the history of the watch. The watch only saves 7 sessions at a time to the watch memory without connecting to an internet database. Viewing the last 7 sessions allows the investigators to assess adherence without relying on the runner to upload data to a server before the participants have completed their training sessions. The average step rate from the last 7 training sessions will be input into an excel spreadsheet and the training sessions will be deleted from the watch. The control group will receive the same device to monitor their pace but receive no instruction to change their preferred step rate. The participant will also receive a training log, but will track their pace and distance for each run. Every participant will perform a 2-3 minute running session on the treadmill after data collection in order to acclimate looking down at the watch, periodically, for 3-5 seconds. This should minimize risk with falling while intermittently looking at the watch for feedback while running overground without supervision. Volunteers will return after 10 in-field training sessions using their monitoring device and a subset of the study participants will return at 6 months to re-assess AVLR and step rate. The intake questionnaire asks if a participant will remain in the Fort Sam Houston area for 7 months after study enrollment. If the participant mark yes, investigators will ask them if the participant would return for a six month follow-up. Investigators will have 30 runners (15 from control group and 15 from retraining group) return for a six month follow-up. The watch has GPS capability to provide accurate feedback on the runner's pace and distance. Investigators will not be monitoring GPS location information for the purpose of this study. All running data will be deleted off the watch when the participant return for their follow-up after the 10 in-field training sessions. A retrospective medical record review, using AHLTA, querying lower extremity injury diagnoses and low back pain will be conducted at six months and at the completion of one year after the retraining program. All volunteers will also receive four email surveys over the year asking them to give their weekly running mileage and (yes/no) if the participant has limited activity due to a running-related overuse injury for one or more days during that quarter. If the answer is yes, the runner will receive additional questions regarding the location and nature of the injury. This quarterly survey is necessary to maximize the accuracy of mileage and injury information to account for mileage conducted and for injuries for which the runner does not seek medical attention. If after 4 weeks the email response rate is less than 50%, the subjects will be contacted by phone to respond to the survey questions. A retrospective profile review, using MODS/Eprofile, querying limited duty days from running-related injuries will be conducted at six months and at the completion of one year after the retraining program. The participants will be required to return the Garmin Watch at the completion of the retraining program or if the participant chooses to leave the study at any time.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Overuse Injury, Lower Extremity Problem, Stress Injury, Repetitive, Patellofemoral Pain Syndrome, Shin Splint
    Keywords
    Running-related lower extremity overuse injuries

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Masking Description
    Participants are masked to group assignment. Investigators are blinded to participant's group at follow-ups.
    Allocation
    Randomized
    Enrollment
    100 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Retraining (RT) Group
    Arm Type
    Experimental
    Arm Description
    The retraining group will receive a watch accelerometer to use for monitoring their step rate with instructions to increase their preferred step rate by 7.5% over the ten in-field training sessions.
    Arm Title
    Control (CON) Group
    Arm Type
    No Intervention
    Arm Description
    The control group will receive the same device to monitor their pace but receive no instruction to change their preferred step rate over the ten in-field training sessions.
    Intervention Type
    Other
    Intervention Name(s)
    Run Gait Retraining
    Intervention Description
    Running step rate will be retrained by real-time biofeedback via a watch accelerometer. Recent literature showed that performing gait retraining by altering step rate reduces loading rates and joint stress that are associated with lower extremity injuries (Wilson et al 2014, Lenhart et al 2014, Heidersheit et al 2011).
    Primary Outcome Measure Information:
    Title
    Change in Average vertical loading rate (AVLR)
    Description
    The slope of the line on a ground reaction force curve from initial contact to the impact peak
    Time Frame
    Baseline, 10 weeks, 6 months
    Title
    Change in Step rate (SR)
    Description
    The number of steps a participant takes per minute of running
    Time Frame
    Baseline, 10 weeks, 6 months
    Title
    Injury
    Description
    The number of lower extremity, over-use injuries sustained within 1 year after completing the ten in-field training sessions
    Time Frame
    1 year
    Secondary Outcome Measure Information:
    Title
    Absolute risk reduction
    Description
    Change in risk for lower extremity, over-use injuries in those that complete step rate retraining
    Time Frame
    1 year
    Title
    Limited duty days
    Description
    Number of days a soldier is non-deployable due to a lower extremity, over-use injury
    Time Frame
    1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    50 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Between the age of 18 - 50 years Active Duty, Department of Defense beneficiaries History of running-related overuse, musculoskeletal injury of the lower extremity (knee, hip, lower leg, or bone stress injury) within the last six months Currently able to run continuously for at least 15 minutes at self-selected pace, 3 times per week. Read and speak English well enough to provide informed consent and follow study instructions Exclusion Criteria: Known pregnancy currently or in the previous 6 months Lower extremity or low back surgery in the previous 6 months Any lower extremity or low back exercise profile that limits running Participant has already completed a step rate, gait retraining program Participant has a step rate greater than 176 steps per minute
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jamie Morris, DPT, DSc
    Phone
    7069739040
    Email
    jamiebushmorris@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    David Boland, DPT, PhD
    Phone
    931-206-9527
    Email
    bolanddpt@gmail.com

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    20581720
    Citation
    Heiderscheit BC, Chumanov ES, Michalski MP, Wille CM, Ryan MB. Effects of step rate manipulation on joint mechanics during running. Med Sci Sports Exerc. 2011 Feb;43(2):296-302. doi: 10.1249/MSS.0b013e3181ebedf4.
    Results Reference
    background
    PubMed Identifier
    25585589
    Citation
    Willson JD, Ratcliff OM, Meardon SA, Willy RW. Influence of step length and landing pattern on patellofemoral joint kinetics during running. Scand J Med Sci Sports. 2015 Dec;25(6):736-43. doi: 10.1111/sms.12383. Epub 2015 Jan 14.
    Results Reference
    background
    PubMed Identifier
    25156044
    Citation
    Lenhart R, Thelen D, Heiderscheit B. Hip muscle loads during running at various step rates. J Orthop Sports Phys Ther. 2014 Oct;44(10):766-74, A1-4. doi: 10.2519/jospt.2014.5575. Epub 2014 Aug 25.
    Results Reference
    background
    PubMed Identifier
    25652871
    Citation
    Willy RW, Buchenic L, Rogacki K, Ackerman J, Schmidt A, Willson JD. In-field gait retraining and mobile monitoring to address running biomechanics associated with tibial stress fracture. Scand J Med Sci Sports. 2016 Feb;26(2):197-205. doi: 10.1111/sms.12413. Epub 2015 Feb 4.
    Results Reference
    background

    Learn more about this trial

    Step Rate Retraining to Reduce Injury and Disability (STRIDe)

    We'll reach out to this number within 24 hrs