Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID05280639

Ankle and Pilon Fracture Post Operative Rehabilitation: A Randomized Control Trial Exploring a Simplified Wooden Block Protocol

Led by University of Virginia · Updated on 2026-06-08

30

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to compare standard post-operative rehabilitation with a simplified wooden block stretching protocol for patients who have ankle or pilon fractures. These fractures are common orthopedic injuries treated by surgery or sometimes by closed reduction and immobilization. The study focuses on reducing stiffness and improving ankle dorsiflexion, which is often limited after cast or splint removal and affects daily activities like walking and stair climbing. Participants will be randomly assigned to one of two groups. One group will follow a simplified rehabilitation program using a wooden block for ankle dorsiflexion exercises at home, with guidance on frequency and technique. The other group will receive standard care through formal physical therapy sessions or a home exercise program based on American Academy of Orthopaedic Surgeons standards. The rehabilitation starts after rigid splint removal, with gradual weight bearing adjusted over the following weeks. During the study, participants will attend three post-operative visits where ankle range of motion will be measured at 2 weeks, 6 weeks, and 6 months after surgery. Researchers will also assess pain, exercise compliance, and lower extremity function through surveys and self-reports. The study aims to evaluate whether the simplified wooden block protocol can improve compliance and functional outcomes compared to usual care, with the total participation lasting six months after surgery.

CONDITIONS

Brief Title

Simplified Post Op Rehabilitation for Ankle and Pilon Fractures

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ages 18 to 65
  • Surgically treated open or closed fractures of the ankle or tibial plafond
Not Eligible

You will not qualify if you...

  • Contralateral lower extremity injuries limiting weight bearing after 6 weeks
  • Severe injury requiring flap coverage or vascular reconstruction (Gustilo-Anderson Type IIIB and C)
  • Neurological deficits that prevent safe standing unassisted for home exercises
  • Desire to participate in formal physical therapy program
  • Additional injuries that limit ability to follow home exercise program
  • Non-ambulatory before injury
  • Previous ankle or tibial plafond injury on the same side
  • Body mass index over 50
  • Severe problems maintaining follow-up
  • Previous ankle or tibial plafond fracture
  • Prisoners
  • Neurological impairments affecting balance or mobility

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Up to 2 weeks until rigid splint removal

Participants undergo surgery to treat ankle or pilon fractures followed by immediate post-operative care.

1 visit for splint removal

Treatment

Duration - 6 weeks following splint removal

Participants begin post-operative rehabilitation using either a simplified wooden block protocol or formal physical therapy/home exercise program to improve ankle dorsiflexion.

3 post-operative visits over 6 weeks

Follow-up

Duration - 6 months after surgery

Participants complete assessments of ankle range of motion, pain, compliance, and lower extremity function at 6 months post-surgery.

1 follow-up visit

Trial Site Locations

Total: 1 location

1

University of Virginia Medical Center

Charlottesville, Virginia, United States, 22908

Actively Recruiting

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Research Team

E

Eric McVey, MEd

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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