NCT02474732

Usability Study for the Beactive Brace Instructions for Use

Assessment of User Comprehension of the BeActive™Brace User Guide

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (actual)
• Sponsor: Benjamin L. England and Associates, LLC · Academic / Other
• Sex: All
• Age: 22 Years – 79 Years
• Healthy volunteers: Accepted

Summary

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.

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.

Conditions

• Lower Back Pain

Interventions

Type	Name	Description
DEVICE	Beactive(r) Brace	Determine if the subjects are able to understand and follow the directions to apply the Beactive Brace.

Timeline

• Start date: 2015-02-01
• Primary completion: 2015-02-01
• Completion: 2015-03-01
• First posted: 2015-06-18
• Last updated: 2017-01-31