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An Osteopathic Assessment of Lower Extremity Somatic Dysfunction in Runners

NCT05132894 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 103

Last updated 2024-06-04

No results posted yet for this study

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.

Conditions

  • Somatic Dysfunction of Sacral Region
  • Somatic Dysfunction of Both Sacroiliac Joints
  • Somatic Dysfunction of Bilateral Lower Extremities

Interventions

OTHER

Osteopathic Assessment

As osteopathic structural exam will be performed to assessment somatic dysfunctions of the lower extremities.

Sponsors & Collaborators

  • The Touro College and University System

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-11-20
Primary Completion
2022-01-20
Completion
2022-02-20

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05132894 on ClinicalTrials.gov