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Evaluation of Heel Offloading Devices for Reducing Heel Contact Pressures in Healthy Volunteers

Primary Purpose

Heel Pressure Ulceration Prevention Strategies

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pillow Condition 1
Pillow Condition 2
Heel Foam Pillow
Offloading Device A
Offloading Device B
Offloading Device C
Sponsored by
DeRoyal Industries, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Heel Pressure Ulceration Prevention Strategies focused on measuring heel, pressure ulcer, pressure mapping

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18 years old or older
  • No musculoskeletal injury in the past month
  • Body Mass Index (BMI) between 18.5 and 39.9

Exclusion Criteria:

  • 17 years old or younger
  • Musculoskeletal injury in the past month
  • Pregnant or lactating female
  • History of heel pressure ulceration
  • BMI below 18.5 or above 39.9

Sites / Locations

  • Lincoln Memorial University; Cedar Bluff Campus

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm Type

No Intervention

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Control

Pillow Condition 1

Pillow Condition 2

Heel Foam Pillow

Offloading Device A

Offloading Device B

Offloading Device C

Arm Description

Pressure mapping is performed without a heel offloading intervention applied.

Pressure mapping is performed with the Pillow condition 1 intervention applied to the heel.

Pressure mapping is performed with the Pillow condition 2 applied to the heel.

Pressure mapping is performed with the heel foam pillow device applied to the heel.

Pressure mapping is performed with Offloading Device A applied to the heel.

Pressure mapping is performed with Offloading Device B applied to the heel.

Pressure mapping is performed with Offloading Device C applied to the heel.

Outcomes

Primary Outcome Measures

Average Contact Force Exerted on the Heel
Average contact force calculated from an area of 40.32 cm^2 that encompassed the entire posterior heel. Pressure readings obtained by pressure mapping
Peak Pressure Index on the Heel
Peak pressure index calculated by centering a 3 X 3 region of interest (14.52 cm^2) over maximum pressure sensor reading within the region of interest encompassing the heel.

Secondary Outcome Measures

Full Information

First Posted
June 21, 2016
Last Updated
January 4, 2018
Sponsor
DeRoyal Industries, Inc.
Collaborators
Lincoln Memorial University
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1. Study Identification

Unique Protocol Identification Number
NCT02811965
Brief Title
Evaluation of Heel Offloading Devices for Reducing Heel Contact Pressures in Healthy Volunteers
Official Title
Evaluation of Heel Offloading Devices for Reducing Heel Contact Pressures in Healthy Volunteers
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
June 2016 (undefined)
Primary Completion Date
November 2016 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
DeRoyal Industries, Inc.
Collaborators
Lincoln Memorial University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Prevention of heel pressure ulceration is a major clinical concern. Clinical research has shown that heel-offloading devices are effective at preventing heel ulceration when compared to no offloading or sub-optimal offloading methods (i.e. use of a hospital pillow to offload the heel). As a result, a plethora of heel-offloading devices have been developed that utilize different designs and materials to offload the heel. Despite the availability of these devices, some healthcare facilities still employ no heel offloading or utilize sub-optimal heel offloading strategies. It is also difficult for clinicians to compare the effectiveness of different heel offloading device without conducting extensive clinical evaluations. Pressure mapping of the pressure experienced by the heel while offloaded offers a potential method to assess the effectiveness of different heel offloading strategies. The primary hypothesis of this study is that the three tested heel offloading devices will significantly decrease the heel contact forces compared to no offloading and sub-optimal heel offloading conditions. The secondary objective is to quantify differences in heel contact forces experienced by the heel when placed in each heel offloading device to demonstrate the utility of pressure mapping as a tool to evaluate the effectiveness of different heel offloading devices. The study will recruit 21 healthy volunteers as research subjects with 7 having a normal BMI, 7 having an overweight BMI, and 7 having an obese BMI. Pressure mapping will be conducted on each research subject for seven randomly applied conditions while the patient lies comfortably in a hospital bed. The seven conditions include no heel offloading, 3 sub-optimal offloading conditions, and offloading in 3 different heel-offloading devices. Pressure measurements corresponding to the heel will be used to determine the average peak pressure contact force for each research subject in each condition.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heel Pressure Ulceration Prevention Strategies
Keywords
heel, pressure ulcer, pressure mapping

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Each research subject will have pressure mapping performed on his or her right foot in the 7 conditions described for each study arm to determine the contact forces experienced by the heel in each off-loading condition. Each intervention will be randomly applied.
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Pressure mapping is performed without a heel offloading intervention applied.
Arm Title
Pillow Condition 1
Arm Type
Experimental
Arm Description
Pressure mapping is performed with the Pillow condition 1 intervention applied to the heel.
Arm Title
Pillow Condition 2
Arm Type
Experimental
Arm Description
Pressure mapping is performed with the Pillow condition 2 applied to the heel.
Arm Title
Heel Foam Pillow
Arm Type
Experimental
Arm Description
Pressure mapping is performed with the heel foam pillow device applied to the heel.
Arm Title
Offloading Device A
Arm Type
Experimental
Arm Description
Pressure mapping is performed with Offloading Device A applied to the heel.
Arm Title
Offloading Device B
Arm Type
Experimental
Arm Description
Pressure mapping is performed with Offloading Device B applied to the heel.
Arm Title
Offloading Device C
Arm Type
Experimental
Arm Description
Pressure mapping is performed with Offloading Device C applied to the heel.
Intervention Type
Other
Intervention Name(s)
Pillow Condition 1
Intervention Description
The heel is offloaded by placing the heel on a standard hospital pillow.
Intervention Type
Other
Intervention Name(s)
Pillow Condition 2
Intervention Description
The heel is offloaded by placing a standard hospital pillow under the calf suspending the heel above the hospital bed mattress.
Intervention Type
Device
Intervention Name(s)
Heel Foam Pillow
Intervention Description
An economy heel offloading device constructed of egg shell foam.
Intervention Type
Device
Intervention Name(s)
Offloading Device A
Intervention Description
Heel offloading device that utilizes open cell foam to offload the heel. Device has a published clinical study demonstrating effectiveness at reducing heel ulceration rate.
Intervention Type
Device
Intervention Name(s)
Offloading Device B
Intervention Description
Heel offloading device that utilizes pressure absorbing filling to offload the heel. Device has a published clinical study demonstrating effectiveness at reducing heel ulceration rate
Intervention Type
Device
Intervention Name(s)
Offloading Device C
Other Intervention Name(s)
PRUventor® Heel Off-loading Device
Intervention Description
Heel offloading device that utilizes a similar pressure absorbing filling to Offloading Device B; however this device does not have published clinical literature demonstrating effectiveness at reducing heel ulceration in the clinic.
Primary Outcome Measure Information:
Title
Average Contact Force Exerted on the Heel
Description
Average contact force calculated from an area of 40.32 cm^2 that encompassed the entire posterior heel. Pressure readings obtained by pressure mapping
Time Frame
5 minutes of pressure mapping
Title
Peak Pressure Index on the Heel
Description
Peak pressure index calculated by centering a 3 X 3 region of interest (14.52 cm^2) over maximum pressure sensor reading within the region of interest encompassing the heel.
Time Frame
5 minutes of pressure mapping

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 years old or older No musculoskeletal injury in the past month Body Mass Index (BMI) between 18.5 and 39.9 Exclusion Criteria: 17 years old or younger Musculoskeletal injury in the past month Pregnant or lactating female History of heel pressure ulceration BMI below 18.5 or above 39.9
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer Savage, DNP
Organizational Affiliation
Lincoln Memorial University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Lincoln Memorial University; Cedar Bluff Campus
City
Knoxville
State/Province
Tennessee
ZIP/Postal Code
37923
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Evaluation of Heel Offloading Devices for Reducing Heel Contact Pressures in Healthy Volunteers

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