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A Self-Directed Web-Based Education for Boston Marathon Runners With Patellofemoral Pain

Boston Children's Hospital logo

Boston Children's Hospital

Status

Not yet enrolling

Conditions

Patellofemoral Pain

Treatments

Behavioral: Education Platform-MyKneeCap.com

Study type

Interventional

Funder types

Other

Identifiers

NCT07266922
IRB-P00052732

Details and patient eligibility

About

Runners experience diverse lower extremity injuries, and the most common is patellofemoral pain (PFP)-commonly known as "runner's knee" and characterized by pain around and/or behind the kneecap. The aim of this study is to evaluate the effectiveness of a 6-week, self-directed, web-based education program for runners competing in the 2026 Boston Marathon. The study will evaluate outcomes, including pain, function, and marathon performance, in runners who use a web-based educational program designed to help them understand and manage knee pain. There will be two groups: Group 1 will receive the 6-week web-based educational program prior to the 2026 Boston Marathon, while Group 2 will serve as the wait-and-see control group (no intervention) prior to the marathon and then receive the same program 6 weeks after completing the marathon.

Enrollment

104 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Insidious onset of peripatellar and/or retropatellar pain ≥3 months
  • Worst pain level in the previous week ≥3/10 on the numeric pain rating scale
  • Pain during at least two of the following tasks: prolonged sitting, kneeling, squatting, walking, running, jumping, and stair negotiation.
  • All participants must have access to an internet-enabled device (e.g., computer, tablet, smartphone) equipped with audio capabilities sufficient to engage with the web-based education platform

Exclusion criteria

  • History of lower extremity surgery
  • History of lower extremity pain or injury (other than patellofemoral pain) in the previous six months
  • History of patellar dislocation or subluxation
  • Internal derangement (e.g., meniscal lesion)
  • Ligamentous instability
  • Other sources of anterior knee pain (e.g., patellar tendinopathy, bursitis)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

104 participants in 2 patient groups

Pre-Marathon Education
Experimental group
Description:
This group will receive the educational platform for 6 weeks prior to the 2026 Boston Marathon. Participants will have access to MyKneeCap.com, a web-based platform designed to provide runners with evidence-based education on the physical and non-physical factors contributing to patellofemoral pain, as well as strategies for self-managing symptoms tailored specifically for runners.
Treatment:
Behavioral: Education Platform-MyKneeCap.com
Wait-and-See Control / Post-Marathon Education
Other group
Description:
This group will serve as a wait-and-see control (no intervention) prior to the 2026 Boston Marathon. After completing the marathon, participants will receive access to MyKneeCap.com, a web-based platform designed to provide runners with evidence-based education on the physical and non-physical factors contributing to patellofemoral pain, as well as strategies for self-managing symptoms tailored specifically for runners.
Treatment:
Behavioral: Education Platform-MyKneeCap.com

Trial contacts and locations

0

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Central trial contact

Olivia Elie; Dai Sugimoto, PhD

Data sourced from clinicaltrials.gov

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