A Study to Evaluate the Mobility+ System and Its Usability

Overview

About this study

The purpose of this study is to determine the sufficiency of the instructions for use, demonstration video, and labeling relating to the Mobility+ system from users, caregivers, and healthcare professionals. This evaluation will enable Rockfield Medical Devices to assess the usability of Mobility+, ensure user and patient safety are prioritized and adequate information on use, precautions, warnings, and contraindications are provided as appropriate.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Group 1: Novices to Home enteral nutrition (Minimum n=15)
Group 2: Non-novices (experienced in enteral feeding) (Minimum n=15)
Group 3: Healthcare professionals (dietitians, nurses) (Minimum of n=15)

Exclusion Criteria:

Users who exclusively use blenderized feed.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status
Rochester, Minn. Mayo Clinic principal investigator Manpreet Mundi, M.D.	Closed for enrollment

Mayo Clinic Location

Status

Rochester, Minn.

Mayo Clinic principal investigator

Manpreet Mundi, M.D.

Closed for enrollment

More information

Publications

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