Changes in the Ankle Range of Motion Following Subtalar Joint Manipulation

July 20, 2018 updated by: Alex Lee, Canadian Memorial Chiropractic College

Changes in the Ankle Range of Motion Following Subtalar Joint Manipulation in Patients With Sub-acute, Grade II, Ankle Inversion Sprains Quantified Using Quaternion Eigen Analysis.

The purpose of the study is to determine whether manipulation of the subtalar joint (one of the two joints of the ankle) has an effect on ankle range of motion in a group of ankles that have sustained a subacute inversion ankle sprain.

The investigators expect subtalar joint manipulation will increase ankle range of motion about the subtalar joint, but not at the talocrural joint (the other joint of the ankle).

Study Overview

Detailed Description

Ankle inversion sprain is a common injury that can cause joint stiffness and range of motion deficits.(Holmer 1994, Beynnon 2001, Denegar 2002, Green 2001) Subtalar joint manipulation has been advocated as an intervention for inversion sprains to reduce pain, decrease joint stiffness, and improve range of motion.(Lopez-Rodriguez 2007)

The ankle is comprised of the talocrural and subtalar joints and their respective joint axes.(Hubbard 2006) Ankle rotation about these axes can be parameterized using quaternions, a four dimensional unit vector. Range of motion (ROM) about these axes can be determined by performing an eigen analysis of the quaternion matrices to determine the root mean squared values of the motion data about these axes.

The objective of the study is to investigate the immediate effects of subtalar joint manipulation on the ROM about the ankle's talocrural and subtalar joints on ankles that have sustained a subacute, grade II inversion sprain.

Forty patients with one sprained ankle and one asymptomatic ankle will be recruited. The subjects will be randomized into either a subtalar manipulation group or a sham manipulation group. The sprained ankle of each patient will receive either a standardized subtalar joint manipulation or a sham manipulation. The same patient's asymptomatic ankle will serve as the non-treatment control group. Range of motion pre- and post-manipulation will be quantified utilizing a quaternion eigen analysis. Kinematic and kinetic parameters will be collected during the manipulation to biomechanically characterize the manipulation. Pain pressure threshold and visual analog scale measurements for pain, stiffness, and quality of movement will be collected.

Our primary hypothesis is subtalar joint manipulation will increase subtalar ROM, but will have no effect on talocrural ROM. Our secondary hypothesis is subtalar joint manipulation will have positive effects on pain, stiffness, and quality of movement.

Study Type

Interventional

Enrollment (Actual)

28

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Ontario
      • Hamilton, Ontario, Canada, L8S 1C7
        • McMaster University
      • Toronto, Ontario, Canada, M2H 3J1
        • Canadian Memorial Chiropractic College

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years to 48 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Must have 1 ankle diagnosed with a subacute, grade II inversion ankle sprain and 1 asymptomatic ankle
  • Pain on palpation of the medial subtalar joint line
  • Manual restriction of subtalar eversion as assessed by a passive joint play test of subtalar joint mobility

Exclusion Criteria: (Pellow 2001, Fryer 2002, Lopez-Rodriguez 2007)

  • Acute ankle or foot trauma occurring within 7 days of injury incident
  • Acute or healing fracture
  • Gross ligamentous mechanical instability (grade III ankle sprains)
  • Syndesmosis injury
  • Inflammatory arthritis
  • History of previous medial ankle sprain
  • Medial ankle instability
  • Severely pronated feet determined by Foot Posture Index score > +9 (Redmond 2006)
  • Connective tissue disorder (Grahame 2000)
  • Benign joint hypermobility syndrome (Grahame 2000)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Subtalar joint manipulation
Each subject in this group will recieve a subtalar joint manipulation to their symptomatic ankle
The intervention is defined as a toggle-recoil, high-velocity, low-amplitude subtalar joint manipulation.
Other Names:
  • Ankle manipulation
Sham Comparator: Sham Manipulation
Each subject in this group will recieve a sham subtalar joint manipulation to their symptomatic ankle
The sham manipulation is conducted by placing the ankle in a non-manipulative position, and the operator simply engages the toggle board to simulate the audible noise of the toggle board dropping. No force or thrust is applied to the ankle.
Other Names:
  • Sham manipulation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Range of Motion determined by a biomechanical ankle model (quaternion eigen analysis)
Time Frame: Outcome measure will be collected immediately pre-manipulation and immediately post-manipulation on day of testing (ie. 1 day)
Outcome measure will be collected immediately pre-manipulation and immediately post-manipulation on day of testing (ie. 1 day)

Secondary Outcome Measures

Outcome Measure
Time Frame
Visual Analog Scales for self-reported pain, stiffness, and quality of movement
Time Frame: Outcome measure will be collected immediately pre-manipulation and immediately post-manipulation on the day of testing (ie. 1 day)
Outcome measure will be collected immediately pre-manipulation and immediately post-manipulation on the day of testing (ie. 1 day)
Pain pressure threshold
Time Frame: Outcome measure will be collected immediately pre-manipulation and immediately post-manipulation on the day of testing (ie. 1 day)
Outcome measure will be collected immediately pre-manipulation and immediately post-manipulation on the day of testing (ie. 1 day)
preload force
Time Frame: Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
peak force
Time Frame: Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
thrust duration
Time Frame: Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
force - time slope
Time Frame: Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
subtalar joint angle
Time Frame: Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
talocrural joint angle
Time Frame: Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)
Outcome measure will be collected during the manipulation on the day of testing (ie. 1 day)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Alexander D Lee, BSc, DC, Canadian Memorial Chiropractic College
  • Study Director: John J Triano, DC, PhD, Canadian Memorial Chiropractic College

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2010

Primary Completion (Actual)

July 16, 2018

Study Completion (Actual)

July 16, 2018

Study Registration Dates

First Submitted

September 21, 2009

First Submitted That Met QC Criteria

September 21, 2009

First Posted (Estimate)

September 22, 2009

Study Record Updates

Last Update Posted (Actual)

July 24, 2018

Last Update Submitted That Met QC Criteria

July 20, 2018

Last Verified

July 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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