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An Osteopathic Assessment of Lower Extremity Somatic Dysfunction in Runners

N/A
Waitlist Available
Research Sponsored by The Touro College and University System
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 8 weeks
Awards & highlights
No Placebo-Only Group

Summary

Runners often experience acute/chronic pain due to pre-existing structural somatic dysfunction and/or acquired various overuse injuries of the lower extremity, specifically affecting the ligaments, tendons, muscles and bones. Common structural and function dysfunctions include but are not limited to patellofemoral pain syndrome (PFPS), Achilles tendonitis, iliotibial band syndrome (ITBS), ligamentous and muscle tears, muscle sprains/strains, stress fractures, pes planus, plantar fasciitis, and shin splints. The purpose of this study is to assess the correlation between acute and chronic pain, overuse injuries, and observational and palpatory findings upon evaluation. With an understanding of the common trends of somatic dysfunctions and etiology of the pain/injury, modified regimen/routine and improved treatment plans can be developed and recommended for runners to better rehabilitate, minimize relapse and reduce compensatory injuries. No medical or osteopathic treatment will be provided.

Eligible Conditions
  • Sacral Dysfunction
  • Sacroiliac Joint Dysfunction
  • Bilateral Lower Extremity Somatic Dysfunction

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 8 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 8 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Questionnaire to analyze data on runners' background/history
Structural exam to determine type of Lower Extremity Somatic Dysfunctions in participants

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

3Treatment groups
Experimental Treatment
Group I: Novice RunnersExperimental Treatment1 Intervention
1-5 miles / week 18+ yo
Group II: Moderate RunnersExperimental Treatment1 Intervention
6-15 miles / week 18+ yo
Group III: Advanced RunnersExperimental Treatment1 Intervention
16+ miles / week 18+ yo

Find a Location

Who is running the clinical trial?

The Touro College and University SystemLead Sponsor
8 Previous Clinical Trials
770 Total Patients Enrolled
~25 spots leftby Jan 2026