Who is eligible for clinical trial NCT06538363?

Participants must meet the protocol's inclusion criteria for Musculoskeletal Injury. The stated age range is 18 Years. Confirm all requirements with the study coordinator.

Does clinical trial NCT06538363 provide travel or cost reimbursement?

Check with the site coordinator at the participating facility for travel and lodging stipend availability, and for which routine-care costs are covered.

🏛️ Verified NIH Record • Updated 2024-08-01

Running Online Injury Prevention Feasibility Study (NCT06538363)

🟡 Not Yet Recruiting Observational / Diagnostic 🧠 Behavioral & Psychological Program Sponsor: Simon Fraser University

🩺 Plain-English Summary (8th-Grade Level)

The main purpose of this study is to test the feasibility of a larger scale interventional study. The investigators want to understand whether data can be reliably collected data various different streams while participants follow a standard 12-week half-marathon training program, and whether participants follow training recommendations.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (8 items) and avoid the listed exclusions (2 items).

Location: Simon Fraser University — Burnaby, British Columbia

Age range: 18 Years

🧪 Interventions in This Study

Education (BEHAVIORAL)
Generic Education (BEHAVIORAL)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Cis-gender female (someone who was born female and currently identifies as a woman) runners
Over the age of 18
Have not been injured in the last 3 months (\*\*For the purpose of this study, an injury is defined as "musculoskeletal (originating from the bones, muscles, joints) that has restricted the ability to run in any way (distance, speed, duration) for at least 7 days or for 3 consecutive training sessions"\*\*)
Have run on average 3 times/week for the last 6 months
Own a GPS-enabled smart watch with an optical wrist heart rate sensor
Fit shoe size between 6.5 and 8.5 US women's sizing
Able to attend one of the in-person orientation sessions
Able to understand written and spoken English

Usually NOT eligible if any of the following apply:

Exclusion Criteria:
Any current pain with running

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (1 Sites)

Simon Fraser University — Burnaby, British Columbia

📞 Contact the Study Coordinator

Phone: (604) 721-1310

Email: cnapier@sfu.ca

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

More studies in Musculoskeletal Injury

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Adaptions and Resiliency to Multi-Stressor OpeRations — Pittsburgh, Pennsylvania
Can Immediate Post-injury Fluoxetine Improve the Recovery Trajectories of Victims in Bodily Trauma? — Gainesville, Florida
Post-Concussion Musculoskeletal Injury Risks — Athens, Georgia

Explore by condition: All Musculoskeletal Injury clinical trials

💡 How to Participate

Check the checklist above to see if you may qualify.
Contact the study coordinator using the phone/email above.
Ask about the visit schedule, what is covered at no cost, and any travel support.
Confirm with your own doctor before making a decision.

🏛️ View Official NIH Record ↗