Usability Study for the Beactive Brace Instructions for Use

Assessment of User Comprehension of the BeActive™Brace User Guide

FDA requires that the user's guide be provided with any over-the-counter (OTC) medical device. It is beneficial to demonstrate that the user's guide for a new medical device is broadly comprehensible where the device will be provided without prescription and direct physician counseling. Therefore, a population of subjects will be tested to determine whether they can properly use the BeActive Brace device after reading the user's guide.

Study Overview

• Status: Completed
• Conditions: Lower Back Pain
• Intervention / Treatment: Device: Beactive(r) Brace

Detailed Description

The primary objective of this clinical trial is to evaluate the ability of approximately 40 literate adults to understand the label instructions for deploying the Beactive(r) Brace device as described in the user's guide, without physician direction. The primary endpoint of this clinical trial is the successful completion of all essential tasks required for Beactive(r) Brace deployment by a subject.

Subjects will be seated at a table facing a video camera, so Investigators and the Sponsor may observe the subject via closed circuit television. Subjects will be given the user's guide for the Beactive(r) Brace device. The subject will then be asked to deploy the Beactive(r) Brace device according to their understanding following the user's guide. For this clinical trial, deploying is defined as completing the following two tasks.

1. Applying the Beactive(r) Brace device to the knee area according to the user's guide.
2. Correctly positioning the pressure pad according to the user's guide.

If the tasks can be completed with no intervention, the subject would be judged to have a "comprehensive" level of success. If intervention was required and helpful, and the subject was able to complete all essential tasks, the level of success would be judged "sufficient." The steps where intervention took place will be recorded.

Intervention will be allowed and documented if subjects have difficulty with a specific task. The subject will raise their hand and a technician will be available for assistance. The frequency and type of intervention will be documented.

A Study Coordinator will complete an observer questionnaire for each subject based on their observation of each subject's ability to use the Beactive device correctly. Each subject will complete a user questionnaire, which will confirm their understanding of the user's guide and give them the opportunity to provide feedback and suggestions for improving the user's guide.

• Study Type: Interventional
• Enrollment (Actual): 40
• Phase: Not Applicable

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 22 years to 79 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Subjects must be male or female, between the ages of ages 22 to 79 years (inclusive);
• Subjects must understand and execute an Individual Consent Form (ICF) and complete a Medical History Form;
• Subjects must be in general good health, except for back pain;
• Subjects must have a history of lower back pain with radiating pain down the leg;
• Subjects must have completed the 10th grade and must be able to read and comprehend English;
• Subjects must be willing to report any medications taken during the trial and refrain from taking medication that might reduce back pain; and
• Subjects must be considered reliable and capable of following directions.

Exclusion Criteria:

• Subjects in ill health or taking medication, other than birth control, which could influence the purpose,integrity or outcome of the trial; or
• Subjects having any visible skin disease, which might be confused with a skin reaction from the test material.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: OTHER
• Allocation: NA
• Interventional Model: SINGLE_GROUP
• Masking: NONE

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Usability; Determine if the subjects are able to understand and follow the directions to apply the Beactive Brace.	Device: Beactive(r) Brace; Determine if the subjects are able to understand and follow the directions to apply the Beactive Brace.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Subjects Correctly Following Instructions for Use	Subjects were observed as they read the instructions for use and applied the Beactive(r) Brace.	Five minutes

Collaborators and Investigators

• Sponsor: Benjamin L. England and Associates, LLC
• Investigators: Study Director: Michael Caswell, Consumer Product Testing Compahy, Inc.

Study record dates

Study Major Dates

• Study Start: February 1, 2015
• Primary Completion (Actual): February 1, 2015
• Study Completion (Actual): March 1, 2015

Study Registration Dates

• First Submitted: June 12, 2015
• First Submitted That Met QC Criteria: June 15, 2015
• First Posted (Estimate): June 18, 2015

Study Record Updates

• Last Update Posted (Estimate): January 31, 2017
• Last Update Submitted That Met QC Criteria: January 30, 2017
• Last Verified: January 1, 2017

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pain; Neurologic Manifestations; Back Pain; Low Back Pain
• Other Study ID Numbers: C15-0419

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO
• IPD Plan Description: Redacted individual participant data is available through the Freedom of Information Act process through the FDA