CFO: Peak Plantar Pressures While Wearing a Carbon Fiber Off Loading Orthoses

Sponsor
Washington University School of Medicine (Other)
Overall Status
Completed
CT.gov ID
NCT03618628
Collaborator
(none)
3
1
1
22.6
0.1

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the ability of carbon fiber off loading orthoses to reduce plantar pressure while providing an augmented plantarflexor power to improve walking and function. Results of this study could lead to increased use of carbon fiber off loading orthoses for patients with diabetes, peripheral neuropathy, and foot wounds as a way augmenting wound healing and preventing future recurrences of wounds.

Condition or Disease Intervention/Treatment Phase
  • Device: Carbon Fiber Off Loading Orthosis (CFO)
N/A

Detailed Description

The long term goal of this research is the successful incorporation of carbon fiber into an off loading device will provide protection to the insensate foot of people with diabetes by reducing localized peak pressures, and thus the risk of recurrence neuropathic foot wounds and fractures, while improving ankle power at push off that will allow individuals with loss of ankle muscle function to walk faster and return to dynamic activities required in their jobs and for full function in the community. The overall goal of this proposal is to determine effects of carbon fiber off loading orthoses (CFO) design characteristics (lay up and geometry of strut) on brace strength, weight, power return capacity, plantar off-loading and participant comfort using FE models, ex-vivo testing and human testing.

First, a CFO will be fabricated using geometry consistent with the current clinical standard. This representative CFO will serve as a baseline from which a finite element (FE) model will be built. The model will be altered as desired to determine the effects of variable design characteristics. The FE model will estimate brace deflection and stress when the CFO is designed with various lay up designs and brace thicknesses. We will use results from the FE model to fabricate a new CFO for study participants.

We will then measure peak plantar pressures during walking while the participants are barefoot, wearing the CFO consistent with current clinical standards, and wearing the new CFO fabricated based on the results of the FE model. We will also measure plantarflexor power during walking while the participants are wearing the CFO consistent with current clinical standards and while wearing the CFO designed based on the results of the FE model. It is believed that the FE model driven CFO design will lead to improved brace strength while reducing plantar pressure compared to barefoot and will have similar plantarflexor power as the CFO based on current clinical standards.

Study Design

Study Type:
Interventional
Actual Enrollment :
3 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Carbon Fiber Off-Loading Orthosis
Actual Study Start Date :
May 24, 2016
Actual Primary Completion Date :
Apr 12, 2018
Actual Study Completion Date :
Apr 12, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: People using a CFO

People who are currently wearing a carbon fiber off loading orthosis (CFO) will have a new CFO fabricated for them based on the results of our finite element (FE) model. We will then test both CFOs ability to reduce peak plantar compared to barefoot and the peak plantarflexor power of both braces.

Device: Carbon Fiber Off Loading Orthosis (CFO)
A finite element (FE) model will be created to determine properties that will improve CFO strength while maintaining reduction of peak plantar pressures of the CFO and plantarflexor power. A new CFO will then be fabricated for the participant. Participants will be tested in while walking barefoot, wearing their current CFO, and wearing the FE model driven CFO.

Outcome Measures

Primary Outcome Measures

  1. Peak Plantar Pressure [Participant was tested in new brace (based on FE model) after wearing for 1 week.]

    Plantar pressure during walking while the participant wears the brace fabricated based on the finite element (FE) model compared to 1) the brace fabricated based on current clinical standards and 2) barefoot.

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Daily life includes a minimum of moderate activity level (variable cadence walking)

  2. Have a Gillette or carbon off loading orthosis as a result of diabetes related foot impairments

  3. Diagnosis of diabetes mellitus and peripheral neuropathy

  4. Ability to ambulate in the community (K-level ≥ 2)

  5. Age > 21 years

Exclusion Criteria:
  1. Unable to ambulate and complete testing required for study participation.

  2. Severe foot deformity of the hindfoot or any deformity of the foot with a dislocation resulting in a bony prominence on the plantar/weightbearing surface of the foot.

  3. Neurological diseases that affects walking

Contacts and Locations

Locations

Site City State Country Postal Code
1 Washington University Saint Louis Missouri United States 63108

Sponsors and Collaborators

  • Washington University School of Medicine

Investigators

  • Principal Investigator: Mary Hastings, DPT, Washington University School of Medicine

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Mary Hastings, PT, DPT, ATC, Professor of Physical Therapy, Orthopaedic Surgery, Washington University School of Medicine
ClinicalTrials.gov Identifier:
NCT03618628
Other Study ID Numbers:
  • 201308105
First Posted:
Aug 7, 2018
Last Update Posted:
May 13, 2019
Last Verified:
May 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

Participant Flow

Recruitment Details
Pre-assignment Detail
Arm/Group Title People Using a CFO
Arm/Group Description People who are currently wearing a carbon fiber off loading orthosis (CFO) will have a new CFO fabricated for them based on the results of our finite element (FE) model. We will then test both CFOs ability to reduce peak plantar compared to barefoot and the peak plantarflexor power of both braces. Carbon Fiber Off Loading Orthosis (CFO): A finite element (FE) model will be created to determine properties that will improve CFO strength while maintaining reduction of peak plantar pressures of the CFO and plantarflexor power. A new CFO will then be fabricated for the participant. Participants will be tested in while walking barefoot, wearing their current CFO, and wearing the FE model driven CFO.
Period Title: Overall Study
STARTED 3
COMPLETED 1
NOT COMPLETED 2

Baseline Characteristics

Arm/Group Title People Using a CFO
Arm/Group Description People who are currently wearing a carbon fiber off loading orthosis (CFO) will have a new CFO fabricated for them based on the results of our finite element (FE) model. We will then test both CFOs ability to reduce peak plantar compared to barefoot and the peak plantarflexor power of both braces. Carbon Fiber Off Loading Orthosis (CFO): A finite element (FE) model will be created to determine properties that will improve CFO strength while maintaining reduction of peak plantar pressures of the CFO and plantarflexor power. A new CFO will then be fabricated for the participant. Participants will be tested in while walking barefoot, wearing their current CFO, and wearing the FE model driven CFO.
Overall Participants 3
Age (Count of Participants)
<=18 years
0
0%
Between 18 and 65 years
1
33.3%
>=65 years
2
66.7%
Age (years) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [years]
66.3
(11.5)
Sex: Female, Male (Count of Participants)
Female
2
66.7%
Male
1
33.3%
Ethnicity (NIH/OMB) (Count of Participants)
Hispanic or Latino
0
0%
Not Hispanic or Latino
3
100%
Unknown or Not Reported
0
0%
Race (NIH/OMB) (Count of Participants)
American Indian or Alaska Native
0
0%
Asian
0
0%
Native Hawaiian or Other Pacific Islander
0
0%
Black or African American
1
33.3%
White
2
66.7%
More than one race
0
0%
Unknown or Not Reported
0
0%
Region of Enrollment (participants) [Number]
United States
3
100%

Outcome Measures

1. Primary Outcome
Title Peak Plantar Pressure
Description Plantar pressure during walking while the participant wears the brace fabricated based on the finite element (FE) model compared to 1) the brace fabricated based on current clinical standards and 2) barefoot.
Time Frame Participant was tested in new brace (based on FE model) after wearing for 1 week.

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title People Using a CFO
Arm/Group Description People who are currently wearing a carbon fiber off loading orthosis (CFO) will have a new CFO fabricated for them based on the results of our finite element (FE) model. We will then test both CFOs ability to reduce peak plantar compared to barefoot and the peak plantarflexor power of both braces. Carbon Fiber Off Loading Orthosis (CFO): A finite element (FE) model will be created to determine properties that will improve CFO strength while maintaining reduction of peak plantar pressures of the CFO and plantarflexor power. A new CFO will then be fabricated for the participant. Participants will be tested in while walking barefoot, wearing their current CFO, and wearing the FE model driven CFO.
Measure Participants 1
Barefoot (midfoot)
75.3
Current CFO (midfoot)
14.2
Model driven CFO (midfoot)
14.5
Barefoot (Forefoot)
22.8
Current CFO (Forefoot)
3.5
Model driven CFO (Forefoot)
6.6
Barefoot (Heel)
60.0
Current CFO (Heel)
23.4
Model driven CFO (Heel)
14.5

Adverse Events

Time Frame Baseline data collected in a brace provided as standard of care. A finite element model was constructed of the brace and provided input for changes in brace construction. This process took 9 months and the participant was tested in the model informed brace 11 months after initial testing
Adverse Event Reporting Description Risks to participants were the possibility of discomfort, blister, or sore while getting used to a new brace and falling during peak plantar pressure testing. Participants were told to contact the study team immediately if any of these they experienced discomfort, blisters, or sores when adapting to the new brace. During peak plantar pressure testing a study team member walked beside the participant holding a gait belt around the waist to make sure they did not fall.
Arm/Group Title People Using a CFO
Arm/Group Description People who are currently wearing a carbon fiber off loading orthosis (CFO) will have a new CFO fabricated for them based on the results of our finite element (FE) model. We will then test both CFOs ability to reduce peak plantar compared to barefoot and the peak plantarflexor power of both braces. Carbon Fiber Off Loading Orthosis (CFO): A finite element (FE) model will be created to determine properties that will improve CFO strength while maintaining reduction of peak plantar pressures of the CFO and plantarflexor power. A new CFO will then be fabricated for the participant. Participants will be tested in while walking barefoot, wearing their current CFO, and wearing the FE model driven CFO.
All Cause Mortality
People Using a CFO
Affected / at Risk (%) # Events
Total 1/3 (33.3%)
Serious Adverse Events
People Using a CFO
Affected / at Risk (%) # Events
Total 0/3 (0%)
Other (Not Including Serious) Adverse Events
People Using a CFO
Affected / at Risk (%) # Events
Total 0/3 (0%)

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

All Principal Investigators ARE employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Results Point of Contact

Name/Title Dr. Mary Hastings
Organization Washington University School of Medicine
Phone 3142861433
Email hastingsmk@wustl.edu
Responsible Party:
Mary Hastings, PT, DPT, ATC, Professor of Physical Therapy, Orthopaedic Surgery, Washington University School of Medicine
ClinicalTrials.gov Identifier:
NCT03618628
Other Study ID Numbers:
  • 201308105
First Posted:
Aug 7, 2018
Last Update Posted:
May 13, 2019
Last Verified:
May 1, 2019