The overarching purpose of this project is to use sensor-derived patterns to guide running interventions during in-field training scenarios for runners with exercise-related lower leg pain. The investigators plan to use the RunScribe sensors to facilitate in-field gait-training to determine the effects of real-time gait-training interventions along with a home exercise program (intervention group) on biomechanical and patient-reported outcome measures of pain and function in runners with leg pain as opposed to receiving a home exercise program alone (control group).
Age range
18 Years – 45 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Change in Contact Time
Timeframe: This outcome change will be assessed from baseline to the end of the intervention (4 weeks) for both groups.
Change in Contact Time Across the Intervention Period
Timeframe: This outcome change will be assessed through study completion over 4 weeks for both groups.
Maintaining Change in Contact Time
Timeframe: This outcome change will be assessed from the end of the intervention (4 weeks) to follow-up at 6 weeks for both groups.
Change in Hip Frontal Plane Motion
Timeframe: This outcome change will be measured from baseline to the end of the intervention (4 weeks) for both groups.
Change in Gluteus Medius Electromyography
Timeframe: This outcome change will be measured from baseline to the end of the intervention (4 weeks) for both groups.
Change in Tibialis Anterior Electromyography
Timeframe: This outcome change will be measured from baseline to the end of the intervention (4 weeks) for both groups.
Change in Pain Outcomes
Timeframe: This outcome change will be assessed from baseline to the end of the intervention (4 weeks) for both groups.
Maintaining Change in Pain Outcomes
Timeframe: This outcome change will be assessed from the end of the intervention (4 weeks) to follow-up at 6 weeks for both groups.
Maintaining Change in Exercise-Induced Leg Pain Questionnaire - British Version Outcomes
Timeframe: This outcome change will be assessed from the end of the intervention (4 weeks) to follow-up at 6 weeks for both groups.
Change in Pain Outcomes Across the Intervention Period
Timeframe: This outcome change will be assessed through study completion over 4 weeks for both groups.
Change in Exercise-Induced Leg Pain Questionnaire - British Version Outcomes
Timeframe: This outcome change will be assessed from baseline to the end of the intervention (4 weeks) for both groups.
Change in Step Rate
Timeframe: This outcome change will be assessed from baseline to the end of the intervention (4 weeks) for both groups.
Change in Stride Length
Timeframe: This outcome change will be assessed from baseline to the end of the intervention (4 weeks) for both groups.
Change in Maximum Pronation Velocity
Timeframe: This outcome change will be assessed from baseline to the end of the intervention (4 weeks) for both groups.
Change in Shock
Timeframe: This outcome change will be assessed from baseline to the end of the intervention (4 weeks) for both groups.
Change in Foot Strike Type
Timeframe: This outcome change will be assessed from baseline to the end of the intervention (4 weeks) for both groups.
Change in Exercise-Induced Leg Pain Questionnaire - British Version Outcomes Across the Intervention Period
Timeframe: This outcome change will be assessed through study completion over 4 weeks for both groups.