Even-Up to Minimize Secondary Site Pain For Ankle Fracture
Primary Purpose
Arthralgia, Trouble Balancing
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Even-Up
Sponsored by
About this trial
This is an interventional prevention trial for Arthralgia focused on measuring Joint pain, Ankle fracture, Leg length discrepancy, CAM boot, Even-Up
Eligibility Criteria
Inclusion Criteria:
- Non-operative Treatment of Ankle Fracture
- CAM boot as treatment for injury
- Weight bearing ad lib
Exclusion Criteria:
- Pregnancy
- Non-English speaking
- Recent surgery for lower extremity or back
- Recent other injury to lower extremity or back
- Restricted weight bearing
Sites / Locations
- Brigham and Women's Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Control
Study
Arm Description
Standard CAM boot treatment without Even-Up device.
CAM boot treatment with Even-Up for contralateral extremity.
Outcomes
Primary Outcome Measures
Patient Reported Pain (VAS)
Visual Analog Scale (0 - 100) to assess pain at various musculoskeletal sites. Patients are presented with a slider on a scale to indicate the degree to which they are experiencing pain on a scale from "No Pain" at the far left to "Worst Pain" at the far right. The position on the scale is then translated into a number from 0 (no pain) to 100 (worst pain).
Patient Reported Outcome (FAAM-ADL, 0 - 100)
FAAM-ADL (Foot and Ankle Ability Measure - Activities of Daily Living, [0 -100]).The FAAM-ADL consists of 21 questions, with a maximum score of 4 per question. The sum of the scores of answered questions is divided by the highest potential score (84 if all 21 questions are answered) and converted to a total score out of 100, with a minimum score of 0. Higher scores indicate better function. Total score range is 0 to 100.
Secondary Outcome Measures
Full Information
NCT ID
NCT04164563
First Posted
November 13, 2019
Last Updated
September 22, 2022
Sponsor
Brigham and Women's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04164563
Brief Title
Even-Up to Minimize Secondary Site Pain For Ankle Fracture
Official Title
A Randomized Controlled Trial of Non-Operative Ankle Fractures: Even-Up Orthotic Shoe Lift and CAM Walking Boot Wear
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Terminated
Why Stopped
We have elected to discontinue enrolling patients.
Study Start Date
November 14, 2019 (Actual)
Primary Completion Date
September 10, 2020 (Actual)
Study Completion Date
September 10, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Evaluating impact of use of Even-Up shoe wear device for patients treated in CAM boot walker for an ankle fracture. Randomized controlled trial, randomizing patients into control group with boot treatment only versus boot treatment with Even-Up device on contralateral extremity.
Detailed Description
A variety of foot and ankle injuries can be treated effectively through the use of a controlled ankle movement (CAM) walker boot. CAM walker boots protect the injured area by restricting foot and ankle motion, providing a stable platform to distribute forces while bearing weight, and allowing the user to rollover the foot during ambulation because of a rocker bottom-shaped sole. Such qualities lend the CAM walker boot to provide ankle support that can be advantageous compared with other commonly used methods. Despite their utility, CAM walker boots create a simulated leg-length discrepancy (LLD), which can result in altered biomechanics during ambulation. Additionally, a LLD can be associated with lower back and joint pain.
We have previously conducted a study that suggests a relationship exists between CAM walker boot treatment and pain at sites other than the extremity being treated. There have been several randomized controlled trials (RCTs) examining a relationship between the correction of inherent LLD with insole inserts and lower back pain. Furthermore, there has been a past RCT and there is a current RCT examining a relationship between the use of the EVENup orthotic shoe lift to correct CAM walker boot simulated LLD and pain at sites other than the extremity being treated. However, these studies were not conducted with patient populations with uniform injuries. To the best of our knowledge, an RCT has not been conducted with the EVENup orthotic shoe lift to examine this relationship in a uniform patient population with nonoperative ankle fractures. This RCT aims to assess the efficacy of the EVENup orthotic shoe lift, towards reducing and even preventing such pain that may be associated with this common course of treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arthralgia, Trouble Balancing
Keywords
Joint pain, Ankle fracture, Leg length discrepancy, CAM boot, Even-Up
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial
Masking
None (Open Label)
Masking Description
Both patients and providers are aware that patients are being assigned to either control or experimental group.
Allocation
Randomized
Enrollment
6 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control
Arm Type
No Intervention
Arm Description
Standard CAM boot treatment without Even-Up device.
Arm Title
Study
Arm Type
Experimental
Arm Description
CAM boot treatment with Even-Up for contralateral extremity.
Intervention Type
Device
Intervention Name(s)
Even-Up
Intervention Description
Orthotic shoe lift worn on contralateral foot to increase leg length
Primary Outcome Measure Information:
Title
Patient Reported Pain (VAS)
Description
Visual Analog Scale (0 - 100) to assess pain at various musculoskeletal sites. Patients are presented with a slider on a scale to indicate the degree to which they are experiencing pain on a scale from "No Pain" at the far left to "Worst Pain" at the far right. The position on the scale is then translated into a number from 0 (no pain) to 100 (worst pain).
Time Frame
0-24 weeks
Title
Patient Reported Outcome (FAAM-ADL, 0 - 100)
Description
FAAM-ADL (Foot and Ankle Ability Measure - Activities of Daily Living, [0 -100]).The FAAM-ADL consists of 21 questions, with a maximum score of 4 per question. The sum of the scores of answered questions is divided by the highest potential score (84 if all 21 questions are answered) and converted to a total score out of 100, with a minimum score of 0. Higher scores indicate better function. Total score range is 0 to 100.
Time Frame
0-24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Non-operative Treatment of Ankle Fracture
CAM boot as treatment for injury
Weight bearing ad lib
Exclusion Criteria:
Pregnancy
Non-English speaking
Recent surgery for lower extremity or back
Recent other injury to lower extremity or back
Restricted weight bearing
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeremy T Smith, MD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02130
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
29685559
Citation
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Results Reference
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Citation
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Results Reference
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Citation
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Results Reference
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Citation
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Citation
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Citation
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Citation
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Citation
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Citation
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Citation
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Citation
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Links:
URL
http://clinicaltrials.gov/ct2/show/NCT03848949
Description
Study of an Orthotic Designed to Equalize Leg Lengths for Patients with Injuries Managed in Walking Boots
Learn more about this trial
Even-Up to Minimize Secondary Site Pain For Ankle Fracture
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