Musculoskeletal InjuryNCT02987517
A Comparative Effectiveness Study of Two Interventions Aimed at Reducing Impact Loads in Runners
A study testing Increased running cadence gait retraining, Forefoot Strike gait retraining and Strengthening exercises in people with Musculoskeletal Injury, run by Spaulding Rehabilitation Hospital.
Trial summary
This study will use a comparative effectiveness design of two interventions known to reduce running impacts. The study will be conducted at the Spaulding National Running Center. Read more about this study
- Who is it for?
- Ages 18 to 50 yearsHealthy volunteers can take part
- Conditions the study is for
- Musculoskeletal Injury
- What is being tested?
- Increased running cadence gait retraining, Forefoot Strike gait retraining and Strengthening exercises
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 39 participants
- Where
- No sites listed yet
- Study dates
- Jan 2016to 31 May 2017
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 50 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- history of running-related injury (outside of the past 3 months)
- ages 18 to 50 years
- currently running 5 to15 miles per week for at least 3 months
- habitual running cadence of less than or equal to 170 steps/min
- no contraindications for exercise as determined by the Physical Activity Readiness Questionnaire (PAR-Q).
Who cannot join
- do not use a heel strike as their habitual gait pattern
- habitual cadence greater than 170 steps/min
- history of injury within the past 3 months
- any history of stress fracture to any bone of the foot or ankle
- any past injuries or surgeries that have permanently altered gait
- color blindness
- Injury will be defined as:
- Running-related (training or competition) musculoskeletal pain in the lower limbs that causes a restriction on or stoppage of running (distance, speed, duration or training) for at least seven days or three consecutive scheduled training sessions, or that requires the runner to consult a physician or other health professional
About this study
Official title: A Prospective Study of Interventions Aimed at Reducing Impact Loads in Runners
This study will use a comparative effectiveness design of two interventions known to reduce running impacts. The study will be conducted at the Spaulding National Running Center. A total of 40 male and female participants, between ages 18-50 years, running 10- 30 miles per week will be recruited from the local running community. All potential subjects will be cleared for physical activity using a Physical Activity Readiness Questionnaire (PAR-Q) and screened via high-speed video to determine their habitual footstrike pattern. Those who are rearfoot strikers will be included and will then be randomized to either an increased cadence (CAD) or a forefoot strike (FFS) intervention group. Standardized running shoes will be provided to both groups for the duration of the study. All participants will attend 2 strength-training instruction sessions with a physical therapist prior to gait-retraining intervention. They will be instructed to perform the learned exercises daily for 4 weeks to prepare the body tissues for forces associated with new gait methods. Subjects will then attend 8 gait-retraining sessions over 2-3 weeks. Sessions will be scheduled as two sequential days of training followed by a day of rest. The gait retraining protocols will be conducted on a treadmill. 3D Motion Capture analysis will be conducted at baseline and at 3 points following intervention (1 week, 1 month, and 6 months).
Read the detailed description
SUBJECT ENROLLMENT
When potential participants are contacted (or contact investigators), they will be screened by phone or email to ensure they meet the study inclusion or exclusion criteria. If they do, details of the study procedures will be explained and they will be given the opportunity to ask questions and take as much time as required to decide if they would like to participate. In addition, once consent is obtained, subjects will undergo an initial screening treadmill run to ensure foot strike and cadence inclusion criteria are met.
Before the study begins, participants will be provided with a written consent form and be given the opportunity to ask any further questions. Prior to initiation of initial screening, data collection, or treatment, participants must sign the consent form.
Participants will be randomly assigned via computer to one of two treatment conditions: 1) increased cadence running gait or 2) forefoot strike running gait.
STUDY PROCEDURES
Subjects will have 13 visits to the Spaulding National Running Center for screening, interventions, and biomechanical analyses. Each visit is outlined below: Visit 1 (2.5 hours) determine if subject uses habitual heel strike and cadence less than or equal to 170, color vision test measure subject's weight, height, leg length, and arch height Baseline biomechanical analysis on instrumented treadmill Physical therapist-researcher will instruct strengthening exercises for feet and legs Subjects told to perform exercises daily and keep journal for 4 weeks
Visit 2 (30 minutes) One week after exercise instruction, subjects meet with a physical-therapist researcher to review and perform strengthening exercises and voice any questions or concerns
Visits 3-10 (1 hour each) Gait retraining on a treadmill using auditory feedback (metronome for cadence or Noraxon system for forefoot strike) and verbal instruction from a physical therapist.
These visits will be distributed over a 2-3 week time period. Subjects may run 2 days in a row, but never 3 days in a row.
Visit 11 (1 week after final gait retraining) (2 hours) Measure subject's resting heart rate, weight, height, leg length, and arch height Biomechanical analysis of running gait on instrumented treadmill Biomechanical analysis of running gait on instrumented treadmill until either 85-90 percent of age predicted heart rate is reached or a Borg Rating of Perceived Exertion score of greater than or equal to 17 is reached.
Subjects instructed in use of REDCap secure web application for journal of running frequency and distance (in miles), any discomfort or injuries that occur with running over the next 6 months.
Visit 12 (1 month after final gait retraining) (2 hours)
Measure subject's weight, height, leg length, and arch height Biomechanical analysis on instrumented treadmill Remind subjects to continue to keep journal
Reminder via email or phone call Physical therapist-researcher will contact subjects 1 time per month over the next 5 months to remind them to continue keeping journal of running frequency and distance (in miles), and any discomfort or injuries that occur.
Visit 13 (6 months after final gait retraining) (2 hours) Measure subject's weight, height, leg length, and arch height Biomechanical analysis on instrumented treadmill
The outcomes to be measured may include any combination of the following:
Structural measures: Height, weight, leg length, arch height. Video analysis: Digital video will only record the waist and below. Motion analysis: recording 3 dimensional movements using a computerized system with reflective markers attached to the body and high-speed cameras.
Ground reaction forces: gathered through force sensing platforms embedded in the treadmill Impact: an accelerometer attached to the body to record the impact experienced by the body with each footstrike.
Devices to be used The data will be collected using 3D motion capture (Vicon Motion Systems) in conjunction with 2 force plates (AMTI), which are embedded in the treadmill. Other devices to be used are foot calipers for arch height, a digital metronome, and an accelerometer with auditory feedback (Noraxon). These are all minimally invasive procedures that involve attaching sensors or markers to the skin and recording the output from the sensor.
- Procedures/interventions All study procedures will take place at the Spaulding National Running Center in the Instrumented Treadmill Lab and clinic. Biomechanical Analysis
All biomechanical analyses of running gait will take place in the Treadmill Lab using an instrumented treadmill (AMTI) and a 3D motion analysis system. Four biomechanical analyses will be conducted over the duration of this investigation. These will occur at baseline, 1 week after the final gait retraining session, 1 month following gait retraining, and 6 months following gait retraining. Procedures for each analysis are as follows:
Subjects will run for a 3 minute warm up and be allowed to adjust to a speed of their preference. An investigator will control treadmill speed, but both participant and investigator can stop the treadmill at anytime via the emergency stop buttons. After warm up, data collection will occur for 4000 frames (15-20 steps). To minimize or prevent any laboratory performance effects, subjects will be distracted during data recording. The distraction technique is based on the Stroop Color and Word Test, and involves subjects reading aloud words on a screen directly in front of the treadmill. The correctness of the test is of no interest; rather, it only serves as a distraction technique.
Fatigue run One week after the final gait retraining session, subjects will be asked to run until they feel fatigued. Fatigue will be defined as either of the following two criteria: when the subject reaches 85-90 percent of age predicted heart rate max or when they report a score greater than or equal to 17 on the Borg Rating of Perceived Exertion scale. Once fatigue is reached, data will be collected for 4000 frames (15-20 steps).
Strengthening exercises During the first visit, a physical-therapist investigator will instruct subjects in strengthening exercises for the feet and legs. These activities will prepare musculoskeletal tissues to adapt to new forces they will experience during gait retraining. Subjects will be instructed to perform the exercises daily for 4 weeks, and will be given a journal to record their exercise performance. One week after exercise instruction, subjects will meet with the physical therapist-investigator to review the strengthening exercises and report any questions or concerns.
Gait Retraining
There will be 8 gait-retraining sessions over a 2-3 week time period. Subjects will be randomly assigned to either an increased cadence gait or a forefoot strike gait. The gait retraining protocols will be conducted on a treadmill (Woodway) in the clinic of the Spaulding National Running Center in the following manner:
Increased cadence (CAD) Protocol: After a 3-minute warm up, subjects' preferred step rate will be determined during their self-selected moderate intensity run for an additional 3 minutes using a visual count of footstrikes. Subjects will then be asked to increase their normal cadence by 7.5 percent while maintaining their speed. This will be accomplished by having subjects match their footstrikes to the beat of an audible digital metronome.
Forefoot strike (FFS) Protocol: Subjects will wear an accelerometer on the right anterior distal tibial. After a 3-minute warm up run, subjects will continue running for an additional 3 minutes and a baseline rearfoot strike accelerometer value will be recorded. Next, subjects will be instructed to land gently on the ball of their foot and lower their heels to the ground. They will be guided with verbal cues and visual inspection from a physical therapist. A forefoot strike accelerometer value will be recorded. If this value is exceeded, the device will provide audible feedback when a heel strike is detected signaling the runner to land with a FFS pattern.
For both groups, run time will be gradually increased from 10-30 minutes over 8 sessions. The auditory feedback will be provided constantly for the first 4 sessions and then gradually decreased in a systematic manner for the last four sessions. This feedback schedule has produced successful outcomes in a number of gait retraining studies.4,5,6 The feedback schedule for both groups is detailed as follows:
Session 1 - 10 minute treadmill run with metronome auditory feedback 100 percent of the time
Sessions 2,3,4 - Time of run will be gradually increased over sessions 2,3,4 to 12, 15, and 18 minutes respectively. Auditory feedback 100 percent of the time.
Sessions 5,6,7,8 - Time of run will be gradually increased over sessions 5,6,7,8 to 21,24,27, and 30 minutes respectively. Auditory feedback will be gradually reduced and given only at the beginning, middle, and end of a run.
This will be 4 minutes for sessions 5; 3 minutes for session 6; 2 minutes for session 7; and 1 minute for session 8.
Participants will be instructed not to run at any other time outside of the gait-retraining period. After completion of gait retraining, subjects will be encouraged to continue their new gait pattern as they run independently in the community. They will be instructed to increase running distance by no greater than 10 percent per week until they reach their desired running duration or distance. Subjects will be asked to keep journals of running activity after gait retraining until they return for the final gait analysis. This will be done via the REDCap (Research Electronic Data Capture) secure web application.
Data to be collected and when the data is to be collected:
Biomechanical outcomes as described above will be collected during each of the 5 biomechanical analyses that participants attend at the Spaulding National Running Center. Every effort will be made to accommodate participants' schedules for these sessions. Data collection will occur at the first visit (baseline), 1 week following gait retraining (approximately 7 to 8 weeks from baseline), 1 month after gait retraining (approximately 11 weeks from baseline), and 6 months after gait retraining (approximately 35 weeks from baseline).
Journals of daily strengthening exercise performance will be collected at Visit 3 (4 weeks from baseline). Journals of running frequency and distance and any discomfort or injuries will be collected throughout the 6 month follow up period using REDCap secure web application (9 to 35 weeks from baseline).
- Conditions
- Musculoskeletal Injury
- Being tested
- Increased running cadence gait retraining, Forefoot Strike gait retraining, Strengthening exercises
- Keywords
- running, vertical load rates, cadence, footstrike
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Increased running cadence gait retrainingOther
Runners use an increased cadence, or step rate, 7.5% greater than baseline preferred cadence
Forefoot Strike gait retrainingOther
Runners use a forefoot strike running gait instead of a rear foot strike running gait.
Strengthening exercisesOther
foot and ankle strengthening exercises performed by all subjects to prepare musculoskeletal tissues for requirements of new running gait.
| Study group | Role | What they receive |
|---|---|---|
| Cadence | Experimental | Runners who use an increased running cadence of 7.5 percent over preferred running cadence. Receives: Other: Increased running cadence gait retraining; Other: Strengthening exercises |
| Forefoot Strike | Experimental | Runners who use a forefoot strike instead of a rear foot strike Receives: Other: Forefoot Strike gait retraining; Other: Strengthening exercises |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Vertical Load Rates
average rate of loading calculated from Vertical Ground Reaction Force
Measured: baseline, 1 week follow up, 1 month follow up, 6 month follow up
Change in Foot Angle
angle of foot in relation to ground, determines foot strike type
Measured: baseline, 1 week follow up, 1 month follow up, 6 month follow up
Change in running cadence (steps per minute)
number of steps taken per minute
Measured: baseline, 1 week follow up, 1 month follow up, 6 month follow up
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Dec 2016 (estimated)
- Study startJan 2016
- Primary completion31 May 2017
- Study completion31 May 2017
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Musculoskeletal InjuryStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 39 participants (actual)
Sponsor and investigators
- Lead sponsor
- Spaulding Rehabilitation Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Irene Sprague Davis, Spaulding Rehabilitation Hospital
- Investigators
- Irene Davis, PhD, Study director, Director, Spaulding National Running Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02987517
- Sponsor's protocol ID
- 2015P000724
- Status last verified
- Apr 2018
- First submitted
- 5 Dec 2016
- Last updated
- 19 Apr 2018
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 Apr 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Prospective Study of Interventions Aimed at Reducing Impact Loads in Runners
- ClinicalTrials.gov ID
- NCT02987517
- Acronym / sponsor ID
- 2015P000724
- Conditions
- Musculoskeletal Injury
- Keywords
- running, vertical load rates, cadence, footstrike
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 39 participants (actual)
- Lead sponsor
- Spaulding Rehabilitation HospitalUniversity, hospital or other
- Study start
- Jan 2016
- Primary completion
- 31 May 2017 (actual)
- Study completion
- 31 May 2017 (actual)
- First posted
- 9 Dec 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study will use a comparative effectiveness design of two interventions known to reduce running impacts. The study will be conducted at the Spaulding National Running Center. A total of 40 male and female participants, between ages 18-50 years, running 10- 30 miles per week will be recruited from the local running community. All potential subjects will be cleared for physical activity using a Physical Activity Readiness Questionnaire (PAR-Q) and screened via high-speed video to determine their habitual footstrike pattern. Those who are rearfoot strikers will be included and will then be randomized to either an increased cadence (CAD) or a forefoot strike (FFS) intervention group. Standardized running shoes will be provided to both groups for the duration of the study. All participants will attend 2 strength-training instruction sessions with a physical therapist prior to gait-retraining intervention. They will be instructed to perform the learned exercises daily for 4 weeks to prepare the body tissues for forces associated with new gait methods. Subjects will then attend 8 gait-retraining sessions over 2-3 weeks. Sessions will be scheduled as two sequential days of training followed by a day of rest. The gait retraining protocols will be conducted on a treadmill. 3D Motion Capture analysis will be conducted at baseline and at 3 points following intervention (1 week, 1 month, and 6 months).
Detailed description
SUBJECT ENROLLMENT
When potential participants are contacted (or contact investigators), they will be screened by phone or email to ensure they meet the study inclusion or exclusion criteria. If they do, details of the study procedures will be explained and they will be given the opportunity to ask questions and take as much time as required to decide if they would like to participate. In addition, once consent is obtained, subjects will undergo an initial screening treadmill run to ensure foot strike and cadence inclusion criteria are met.
Before the study begins, participants will be provided with a written consent form and be given the opportunity to ask any further questions. Prior to initiation of initial screening, data collection, or treatment, participants must sign the consent form.
Participants will be randomly assigned via computer to one of two treatment conditions: 1) increased cadence running gait or 2) forefoot strike running gait.
STUDY PROCEDURES
Subjects will have 13 visits to the Spaulding National Running Center for screening, interventions, and biomechanical analyses. Each visit is outlined below: Visit 1 (2.5 hours) determine if subject uses habitual heel strike and cadence less than or equal to 170, color vision test measure subject's weight, height, leg length, and arch height Baseline biomechanical analysis on instrumented treadmill Physical therapist-researcher will instruct strengthening exercises for feet and legs Subjects told to perform exercises daily and keep journal for 4 weeks
Visit 2 (30 minutes) One week after exercise instruction, subjects meet with a physical-therapist researcher to review and perform strengthening exercises and voice any questions or concerns
Visits 3-10 (1 hour each) Gait retraining on a treadmill using auditory feedback (metronome for cadence or Noraxon system for forefoot strike) and verbal instruction from a physical therapist.
These visits will be distributed over a 2-3 week time period. Subjects may run 2 days in a row, but never 3 days in a row.
Visit 11 (1 week after final gait retraining) (2 hours) Measure subject's resting heart rate, weight, height, leg length, and arch height Biomechanical analysis of running gait on instrumented treadmill Biomechanical analysis of running gait on instrumented treadmill until either 85-90 percent of age predicted heart rate is reached or a Borg Rating of Perceived Exertion score of greater than or equal to 17 is reached.
Subjects instructed in use of REDCap secure web application for journal of running frequency and distance (in miles), any discomfort or injuries that occur with running over the next 6 months.
Visit 12 (1 month after final gait retraining) (2 hours)
Measure subject's weight, height, leg length, and arch height Biomechanical analysis on instrumented treadmill Remind subjects to continue to keep journal
Reminder via email or phone call Physical therapist-researcher will contact subjects 1 time per month over the next 5 months to remind them to continue keeping journal of running frequency and distance (in miles), and any discomfort or injuries that occur.
Visit 13 (6 months after final gait retraining) (2 hours) Measure subject's weight, height, leg length, and arch height Biomechanical analysis on instrumented treadmill
The outcomes to be measured may include any combination of the following:
Structural measures: Height, weight, leg length, arch height. Video analysis: Digital video will only record the waist and below. Motion analysis: recording 3 dimensional movements using a computerized system with reflective markers attached to the body and high-speed cameras.
Ground reaction forces: gathered through force sensing platforms embedded in the treadmill Impact: an accelerometer attached to the body to record the impact experienced by the body with each footstrike.
Devices to be used The data will be collected using 3D motion capture (Vicon Motion Systems) in conjunction with 2 force plates (AMTI), which are embedded in the treadmill. Other devices to be used are foot calipers for arch height, a digital metronome, and an accelerometer with auditory feedback (Noraxon). These are all minimally invasive procedures that involve attaching sensors or markers to the skin and recording the output from the sensor.
- Procedures/interventions All study procedures will take place at the Spaulding National Running Center in the Instrumented Treadmill Lab and clinic. Biomechanical Analysis
All biomechanical analyses of running gait will take place in the Treadmill Lab using an instrumented treadmill (AMTI) and a 3D motion analysis system. Four biomechanical analyses will be conducted over the duration of this investigation. These will occur at baseline, 1 week after the final gait retraining session, 1 month following gait retraining, and 6 months following gait retraining. Procedures for each analysis are as follows:
Subjects will run for a 3 minute warm up and be allowed to adjust to a speed of their preference. An investigator will control treadmill speed, but both participant and investigator can stop the treadmill at anytime via the emergency stop buttons. After warm up, data collection will occur for 4000 frames (15-20 steps). To minimize or prevent any laboratory performance effects, subjects will be distracted during data recording. The distraction technique is based on the Stroop Color and Word Test, and involves subjects reading aloud words on a screen directly in front of the treadmill. The correctness of the test is of no interest; rather, it only serves as a distraction technique.
Fatigue run One week after the final gait retraining session, subjects will be asked to run until they feel fatigued. Fatigue will be defined as either of the following two criteria: when the subject reaches 85-90 percent of age predicted heart rate max or when they report a score greater than or equal to 17 on the Borg Rating of Perceived Exertion scale. Once fatigue is reached, data will be collected for 4000 frames (15-20 steps).
Strengthening exercises During the first visit, a physical-therapist investigator will instruct subjects in strengthening exercises for the feet and legs. These activities will prepare musculoskeletal tissues to adapt to new forces they will experience during gait retraining. Subjects will be instructed to perform the exercises daily for 4 weeks, and will be given a journal to record their exercise performance. One week after exercise instruction, subjects will meet with the physical therapist-investigator to review the strengthening exercises and report any questions or concerns.
Gait Retraining
There will be 8 gait-retraining sessions over a 2-3 week time period. Subjects will be randomly assigned to either an increased cadence gait or a forefoot strike gait. The gait retraining protocols will be conducted on a treadmill (Woodway) in the clinic of the Spaulding National Running Center in the following manner:
Increased cadence (CAD) Protocol: After a 3-minute warm up, subjects' preferred step rate will be determined during their self-selected moderate intensity run for an additional 3 minutes using a visual count of footstrikes. Subjects will then be asked to increase their normal cadence by 7.5 percent while maintaining their speed. This will be accomplished by having subjects match their footstrikes to the beat of an audible digital metronome.
Forefoot strike (FFS) Protocol: Subjects will wear an accelerometer on the right anterior distal tibial. After a 3-minute warm up run, subjects will continue running for an additional 3 minutes and a baseline rearfoot strike accelerometer value will be recorded. Next, subjects will be instructed to land gently on the ball of their foot and lower their heels to the ground. They will be guided with verbal cues and visual inspection from a physical therapist. A forefoot strike accelerometer value will be recorded. If this value is exceeded, the device will provide audible feedback when a heel strike is detected signaling the runner to land with a FFS pattern.
For both groups, run time will be gradually increased from 10-30 minutes over 8 sessions. The auditory feedback will be provided constantly for the first 4 sessions and then gradually decreased in a systematic manner for the last four sessions. This feedback schedule has produced successful outcomes in a number of gait retraining studies.4,5,6 The feedback schedule for both groups is detailed as follows:
Session 1 - 10 minute treadmill run with metronome auditory feedback 100 percent of the time
Sessions 2,3,4 - Time of run will be gradually increased over sessions 2,3,4 to 12, 15, and 18 minutes respectively. Auditory feedback 100 percent of the time.
Sessions 5,6,7,8 - Time of run will be gradually increased over sessions 5,6,7,8 to 21,24,27, and 30 minutes respectively. Auditory feedback will be gradually reduced and given only at the beginning, middle, and end of a run.
This will be 4 minutes for sessions 5; 3 minutes for session 6; 2 minutes for session 7; and 1 minute for session 8.
Participants will be instructed not to run at any other time outside of the gait-retraining period. After completion of gait retraining, subjects will be encouraged to continue their new gait pattern as they run independently in the community. They will be instructed to increase running distance by no greater than 10 percent per week until they reach their desired running duration or distance. Subjects will be asked to keep journals of running activity after gait retraining until they return for the final gait analysis. This will be done via the REDCap (Research Electronic Data Capture) secure web application.
Data to be collected and when the data is to be collected:
Biomechanical outcomes as described above will be collected during each of the 5 biomechanical analyses that participants attend at the Spaulding National Running Center. Every effort will be made to accommodate participants' schedules for these sessions. Data collection will occur at the first visit (baseline), 1 week following gait retraining (approximately 7 to 8 weeks from baseline), 1 month after gait retraining (approximately 11 weeks from baseline), and 6 months after gait retraining (approximately 35 weeks from baseline).
Journals of daily strengthening exercise performance will be collected at Visit 3 (4 weeks from baseline). Journals of running frequency and distance and any discomfort or injuries will be collected throughout the 6 month follow up period using REDCap secure web application (9 to 35 weeks from baseline).
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Cadence | Experimental | Other: Increased running cadence gait retraining, Other: Strengthening exercisesRunners who use an increased running cadence of 7.5 percent over preferred running cadence. |
| Forefoot Strike | Experimental | Other: Forefoot Strike gait retraining, Other: Strengthening exercisesRunners who use a forefoot strike instead of a rear foot strike |
Who may qualify
- Ages
- 18 to 50 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (5 listed)
- history of running-related injury (outside of the past 3 months)
- ages 18 to 50 years
- currently running 5 to15 miles per week for at least 3 months
- habitual running cadence of less than or equal to 170 steps/min
- no contraindications for exercise as determined by the Physical Activity Readiness Questionnaire (PAR-Q).
Key exclusion criteria (8 listed)
- do not use a heel strike as their habitual gait pattern
- habitual cadence greater than 170 steps/min
- history of injury within the past 3 months
- any history of stress fracture to any bone of the foot or ankle
- any past injuries or surgeries that have permanently altered gait
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Increased running cadence gait retrainingRunners use an increased cadence, or step rate, 7.5% greater than baseline preferred cadence | Other | Cadence |
| Forefoot Strike gait retrainingRunners use a forefoot strike running gait instead of a rear foot strike running gait. | Other | Forefoot Strike |
| Strengthening exercisesfoot and ankle strengthening exercises performed by all subjects to prepare musculoskeletal tissues for requirements of new running gait. | Other | Cadence, Forefoot Strike |
Primary outcome
Change in Vertical Load Rates
Time frame: baseline, 1 week follow up, 1 month follow up, 6 month follow up
average rate of loading calculated from Vertical Ground Reaction Force
Change in Foot Angle
Time frame: baseline, 1 week follow up, 1 month follow up, 6 month follow up
angle of foot in relation to ground, determines foot strike type
Change in running cadence (steps per minute)
Time frame: baseline, 1 week follow up, 1 month follow up, 6 month follow up
number of steps taken per minute
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Apr 2018.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Irene Davis, PhD study director
Director, Spaulding National Running Center
Questions about this trial
What is this clinical trial studying?
A study testing Increased running cadence gait retraining, Forefoot Strike gait retraining and Strengthening exercises in people with Musculoskeletal Injury, run by Spaulding Rehabilitation Hospital.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 19 Apr 2018. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Vertical Load Rates (time frame: baseline, 1 week follow up, 1 month follow up, 6 month follow up). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Apr 2018; AzTrials last refreshed its copy on 2 Nov 2026.