Last reviewed · How we verify
NCT04747223: STRIDe
Step Rate Retraining to Reduce Injury and Disability (STRIDe)
NA trial testing Run Gait Retraining in Overuse Injury in 100 participants. Status unknown.
1 June 2022
Quick facts
| Lead sponsor | Army-Baylor University Doctoral Program in Physical Therapy |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | prevention |
| Enrollment | 100 |
| Start date | 1 February 2021 |
| Primary completion | 1 June 2022 |
| Estimated completion | 31 December 2022 |
Drugs / interventions tested
- Run Gait Retraining
Conditions studied
- Overuse Injury — all drugs for Overuse Injury →
- Lower Extremity Problem — all drugs for Lower Extremity Problem →
- Stress Injury, Repetitive — all drugs for Stress Injury, Repetitive →
- Patellofemoral Pain Syndrome — all drugs for Patellofemoral Pain Syndrome →
Sponsor
Army-Baylor University Doctoral Program in Physical Therapy
Who can join
Adults 18 to 50, any sex, with Overuse Injury or Lower Extremity Problem. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT04747223
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Related trials
Other Army-Baylor University Doctoral Program in Physical Therapy trials
Trials by the same sponsor.
- NCT04170803 — Feasibility of Near-infrared Spectroscopy to Measure Cortical Pain Pathway (Brain) Activation During Dry Needling · EARLY_PHASE1 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04747223 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Army-Baylor University Doctoral Program in Physical Therapy
- Last refreshed: 10 February 2021
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04747223.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing