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NCT04269473
Video Telehealth Gait Retraining for Running-Related Knee Pain
NA trial testing Telehealth Gait Retraining in Telemedicine in 180 participants. Completed in 1 December 2024.
1 December 2024
Quick facts
| Lead sponsor | Keller Army Community Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | supportive care |
| Enrollment | 180 |
| Start date | 14 August 2020 |
| Primary completion | 1 December 2024 |
| Estimated completion | 1 December 2024 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Telehealth Gait Retraining
- Standard Physical Therapy Treatment
- Return to Running Protocol
- At Home Exercise Program
Conditions studied
- Telemedicine — all drugs for Telemedicine →
- Running — all drugs for Running →
- Knee — all drugs for Knee →
- Pain — all drugs for Pain →
Sponsor
Keller Army Community Hospital
Who can join
Adults 18 to 60, any sex, with Telemedicine or Running. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
In this randomized control trial, participants with running-related knee pain will be randomly assigned to either an intervention group or a control group. Participants in the intervention group will receive a telehealth gait retraining intervention, an at-home exercise program, a return to running protocol, and standard physical therapy. Participants in the control group will receive an at-home exercise program, a return to running protocol, and standard physical therapy. Data will be collected before intervention, at 10-weeks, and at 14-weeks to determine efficacy of the intervention.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
The effectiveness of telehealth gait retraining in addition to standard physical therapy treatment for overuse knee injuries in soldiers: a protocol for a randomized clinical trial.
Crowell MS, Brindle RA, Miller EM, Reilly N, et al · · 2023 · PMID 37845752 · DOI 10.1186/s13063-023-07502-x -
The Effectiveness of Telehealth Gait Retraining in Addition to Standard Physical Therapy Treatment for Overuse Knee Injuries in Soldiers: A Protocol for a Randomized Clinical Trial
Crowell M, Brindle R, Miller E, Reilly N, et al · · 2023 · DOI 10.21203/rs.3.rs-2492896/v1
Verify or expand the search:
- PubMed search for NCT04269473
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Keller Army Community Hospital trials
Trials by the same sponsor.
- NCT06988709 — Examining the Most Effective Method to Reduce Running Ground Contact Time · NA · recruiting
- NCT05453110 — Does Self-efficacy Predict Outcomes Among U.S. Military Academy Cadets During Initial Entry Training? · NA · completed
- NCT05506072 — Blood Flow Restriction Training Versus Standard Physical Therapy After Shoulder Stabilization Surgery · NA · completed
- NCT04902274 — Effectiveness of Transcranial Direct Current Stimulation (tDCS). · NA · terminated
- NCT07187024 — Efficacy of an Evidence-based Telehealth Intervention in Modifying Health Behavior · NA · active not recruiting
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 NCT04269473 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Keller Army Community Hospital
- Last refreshed: 21 May 2025
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/NCT04269473.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing