Simplified Post Op Rehabilitation for Ankle and Pilon Fractures

NCT ID: NCT05280639

Last Updated: 2025-05-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-10-03

Study Completion Date

2025-12-01

Brief Summary

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The aim of this study is to compare standard post operative rehabilitation with a simplified wooden block stretching protocol that will yield similar results.

Detailed Description

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Ankle fractures and pilon fractures represent common injuries in orthopedics. These injuries are addressed with re-aligning the bones with surgery, and in some particular cases, they are treated closed reduction and immobilization during healing. The trauma to the ankle as a result of the injury, the prolonged immobilization in a cast or splint and the scar tissue formed during surgery often lead to post injury and post-operative stiffness. Many patients have limited ability to flex the ankle upward (dorsiflexion) following cast or splint removal for these injuries. Physical therapy and rehabilitation represent an an industry-accepted practice for alleviating stiffness and improving function. Currently there are varying studies on the benefits of manual therapy or passive stretch when compared with exercise alone. Neither a supervised exercise program such as formal physical therapy nor a home exercise regiment offer a clear benefit over the other, leading to the question of, if this process can be further simplified to use with the wooden block.

The main functional complaint of patients is "stiffness" or decreased range of motion is in dorsiflexion of the ankle and is cited at approximately 77% of patients following cast or splint removal. This motion is key when walking normally, descending stairs or kneeling and is important to a greater degree when walking up hills , running or rising from a chair. These activities require 10 degrees passive dorsiflexion and 20 degrees on average, respectively. The functional effects of limited ankle dorsiflexion sometimes results in the need for a shoe heel insert or additional surgical procedures to free up the scar in the front of the ankle.

This randomized control trial aims to analyze two currently-used standards of care for ankle and tibial plafond injuries, simplifying the standard post-operative physical therapy/rehabilitation regiment, which would begin a the time of rigid splint removal, when stretching and range of motion is tolerated. Weight bearing with ambulation is slowly adjusted for the weeks following this. This simplified wooden block protocol ankle exercises focus strictly on ankle dorsiflexion using a wooden block. The investigators aim of doing so is to increase compliance with the exercises and with an improved functional outcome as compared with the standard, more complex exercises and time burdensome options.

The aim of this study is to compare the standard post injury/surgery rehabilitation with this new simplified wooden block stretching protocol and analyze the simplified protocol's effectiveness verses other industry accepted exercises/therapy regiments. This study will evaluate pain scores, compliance, range of motion of the ankle and include a Lower Extremity Functionality Score survey, over the course of 3 standard post-operative visits following the subjects injury.

Conditions

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Ankle Fractures Pilon Fracture

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Simplified block protocol

subjects in this group will perform a simplified post operative rehabilitation program using a simplified wooden block protocol

Group Type EXPERIMENTAL

Wooden block

Intervention Type DEVICE

Individuals randomized to this group will be given a wooden block at no cost to them and a simplified version of home, self-guided exercises with instructions on how to do the exercises and how often to do so.

Usual care

Subjects in this group will perform formal physical therapy or a home exercise program consistent with AAOS standards.

Group Type ACTIVE_COMPARATOR

Formal physical therapy or Home Exercise Program

Intervention Type OTHER

Individuals randomized to this group will receive the standard formal physical therapy which are sessions run by a physical therapist, usually 2-3 times a week to rehabilitate their ankle OR follow a standardized home exercise program which will be done by yourself with exercise outlined with how they should be performed and how often

Interventions

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Wooden block

Individuals randomized to this group will be given a wooden block at no cost to them and a simplified version of home, self-guided exercises with instructions on how to do the exercises and how often to do so.

Intervention Type DEVICE

Formal physical therapy or Home Exercise Program

Individuals randomized to this group will receive the standard formal physical therapy which are sessions run by a physical therapist, usually 2-3 times a week to rehabilitate their ankle OR follow a standardized home exercise program which will be done by yourself with exercise outlined with how they should be performed and how often

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Ages 18-65
* Surgically treated open or closed fractures of the ankle or tibial plafond

Exclusion Criteria

* Contralateral lower extremity injuries that would limit weight bearing after 6 weeks
* Severe injury requiring flap coverage or vascular reconstruction (Gustilo-Anderson Type IIIB and C respectively)
* Neurological deficits that would impede ability to stand safely unassisted for home exercise regiment
* Desire to participate in formal physical therapy program
* Additional injury that would compromise subjects ability to follow either Home Exercise Program
* Non ambulatory prior to injury
* Previous ankle or tibial plafond injury on ipsilateral extremity
* BMI \> 50
* Severe problems maintaining follow up
* Previous ankle/tibial plafond fracture
* Prisoners
* Neurological impairments that impair balance
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Virginia

OTHER

Sponsor Role lead

Responsible Party

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Seth Yarboro, MD

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Seth Yarboro, MD

Role: PRINCIPAL_INVESTIGATOR

University of Virginia Orthopaedic Surgey

Locations

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University of Virginia Medical Center

Charlottesville, Virginia, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Eric McVey, MEd

Role: CONTACT

434.243.5382

Facility Contacts

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Lori Elder

Role: primary

434-924-8570

Other Identifiers

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HSR200191

Identifier Type: -

Identifier Source: org_study_id

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