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Effectiveness of Jamboxx Respiratory Therapy Device: Study 1

Primary Purpose

Spinal Cord Injuries, Respiratory Complication

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Jamboxx Respiratory Therapy Device
Jamboxx Musical Device
Sponsored by
My Music Machines Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinal Cord Injuries focused on measuring respiratory therapy, videogaming therapy, incentive spirometry

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Quadriplegic and other spinal cord injury outpatients will be included.

Exclusion Criteria:

  • Individuals already adhering to a daily regimen of prescribed respiratory therapy routine will be excluded.

Sites / Locations

  • Albany Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Group 1

Group 2

Arm Description

Group 1 (control group) will be given the standard Jamboxx musical device. They will be trained to use the device during two 20 minute training session with a respiratory therapist, and will be instructed to play the device for a minimum of 30 minutes, 3 times a week. The Jamboxx musical device is a hands-free breath controlled musical device designed for people with quadriplegia. The mouthpiece acts as a transducer, changing air pressure created by the user's lungs to a joystick signal to the computer via a differential pressure sensor. The Jamboxx can produce musical sounds of many instruments (trumpet, drums, etc.) in many different scales and in any key.

Group 2 (treatment group) will be given the Jamboxx musical device plus the Jamboxx respiratory therapy device. The respiratory therapy device is similar to the music device, but with specially designed games that guide the user through breathing exercises intended to strengthen the lungs.

Outcomes

Primary Outcome Measures

Change in Self-Reported Patient Dyspnea
Change in patient reported measure of breathlessness during daily activities from baseline over the course of the 1 year study

Secondary Outcome Measures

Multidimensional Dyspnea Profile
A measure of breathlessness after performing an activity
Dyspnea-12 Questionnaire
A survey that measures recent breathlessness with 12 questions related to dyspnea, each evaluated on a scale of 0-4 (0=none, 1=mild, 2=moderate, 3=severe) that indicate how troubled people are by each of these 12 topics, for a total possible score ranging from 0 to 36, where lower scores relate to better outcomes.
FEV1
measure of pulmonary function (Forced Expiratory Volume over 1 second) measured in liters
FVC
measure of pulmonary function (Forced Vital Capacity) measured in liters
PEF
measure of pulmonary function (Peak Expiratory Flow) measured in liters
MEP
measure of pulmonary function (Maximum Expiratory Pressure) measured in centimeters of H2O
MIP
measure of pulmonary function (maximum inspiratory pressure) measured in centimeters of H2O
Device usability
Measurement of enjoyment and engagement with the intervention via survey
Clinically relevant events
e.g. patient being sent for a chest x-ray, being ordered chest physiotherapy or blood tests
Patient Empowerment
Measured via a single question ranked on a likert scale: "I believe that this respiratory therapy empowered me to protect my breathing" With answer options of 1. strongly disagree, 2. disagree, 3. neutral, 4. agree, 5. strongly agree, with higher numbers corresponding to better outcomes

Full Information

First Posted
April 26, 2018
Last Updated
May 11, 2020
Sponsor
My Music Machines Inc.
Collaborators
Albany Medical College, National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT03533400
Brief Title
Effectiveness of Jamboxx Respiratory Therapy Device: Study 1
Official Title
The Effectiveness of the Jamboxx Respiratory Therapy Device in Treatment of Patients With Decreased Respiratory Function. Study 1: Spinal Cord Injury Patients for Long Term Evaluation
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Withdrawn
Why Stopped
NHLBI has suggested the company focus on the other two ongoing trials
Study Start Date
December 1, 2019 (Anticipated)
Primary Completion Date
December 31, 2019 (Anticipated)
Study Completion Date
December 31, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
My Music Machines Inc.
Collaborators
Albany Medical College, National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The Effectiveness of the Jamboxx Respiratory Therapy Device in Treatment of Patients with Decreased Respiratory Function is a proposal for investigation of the application of gaming to improving respiratory health. The Jamboxx device combines gaming with traditional incentive spirometry to provide users with a fun experience to keep them engaged in their respiratory therapy routine. The device allows users to play a series of mini-games that walk them through their routines. The Jamboxx also records airflow and lung parameters with an external mouthpiece attachment to provide users with real time feedback, and helps to assess increases or decreases in relative lung function over time. The Jamboxx has the potential to significantly impact the field of respiratory therapy by being one of the first gaming devices for patient therapy, and the first respiratory therapy gaming device that is accessible to users with limited mobility. Jamboxx provides a fun and engaging, low cost alternative to the traditional therapy techniques used and aims to improve patient compliance.
Detailed Description
Study 1 addresses the concerns of pneumonia risks in quadriplegics with compromised respiratory pump mechanics. In cases of spinal cord injury or high-level motor neuron disease, complications with respiratory function are a common concern. Lack of innervation to the intercostal and abdominal muscles can cause a decline in respiratory capacity as well as overall lung function, with associated increased risk of mortality. Shallow tidal breathing and impaired or absent cough results in morbidity and mortality from pneumonia. Several studies have found failure of the respiratory system, including pneumonia, to be a leading cause of mortality among spinal cord injury patients. In order to maintain pulmonary health, many people with quadriplegia and other high-level motor neuron diseases undergo routine respiratory therapy to help stretch the muscles around the lungs, exercise the diaphragm, and loosen mucus build-up. Incentive spirometry is one commonly used component of respiratory therapy designed to mimic natural sighing or yawning by encouraging the patient to take long, slow, deep breaths. This is done with an incentive spirometer device, which provides patients with visual or other positive feedback with a piston or a ball that moves inside a gauge. Respiratory therapy techniques are also used to help maintain pulmonary health in individuals with a number of chronic or temporary respiratory diseases and conditions such as asthma, chronic obstructive pulmonary disease, and emphysema. These techniques often become strenuous and mundane for users with limited mobility, and thus patient compliance rates are low. Gaming controlled by forceful respiratory maneuvers will be studied to ascertain if respiratory mechanics can be improved in this group. Testing Plan: Study participants will be randomized into 2 groups through drawing of sealed envelopes. Group 1 (control group) will be given the standard Jamboxx musical device (see appendix a for device details), while Group 2 (treatment group) will be given the Jamboxx respiratory therapy device, which combines musical gameplay with incentive spirometry exercises. Participants from both groups will have two 20 minute training sessions with the device: one initial training visit and one follow up visit. Training sessions will take place either in the home, or at Albany Medical Center. During the initial visit a simple spirometry test (FEV1, FVC and PEF) and maximum inspiratory and expiratory pressures (MIP and MEP) will be performed. These functions will be measured again at 3, 6, 9 & 12 months by a respiratory therapist (RT). The Dyspnea-12 (D-12) questionnaire will be conducted at by the RT at months 0, 3, 6, 9, and 12. Self-Reported Patient Dyspnea and the Multidimensional Dyspnea Profile (MDP) will be reported electronically by study participants on a weekly basis. Medical records will be evaluated for relevant health history, medication use, and hospitalizations including dates. Access to medical records will be obtained by a signed medical release form.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injuries, Respiratory Complication
Keywords
respiratory therapy, videogaming therapy, incentive spirometry

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Study participants will be randomized into 2 groups via random number generator. Group 1 (control group) will be given the standard Jamboxx musical device, while Group 2 (treatment group) will be given the Jamboxx respiratory therapy device, which combines musical gameplay with incentive spirometry exercises.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
Active Comparator
Arm Description
Group 1 (control group) will be given the standard Jamboxx musical device. They will be trained to use the device during two 20 minute training session with a respiratory therapist, and will be instructed to play the device for a minimum of 30 minutes, 3 times a week. The Jamboxx musical device is a hands-free breath controlled musical device designed for people with quadriplegia. The mouthpiece acts as a transducer, changing air pressure created by the user's lungs to a joystick signal to the computer via a differential pressure sensor. The Jamboxx can produce musical sounds of many instruments (trumpet, drums, etc.) in many different scales and in any key.
Arm Title
Group 2
Arm Type
Experimental
Arm Description
Group 2 (treatment group) will be given the Jamboxx musical device plus the Jamboxx respiratory therapy device. The respiratory therapy device is similar to the music device, but with specially designed games that guide the user through breathing exercises intended to strengthen the lungs.
Intervention Type
Device
Intervention Name(s)
Jamboxx Respiratory Therapy Device
Intervention Description
Jamboxx Respiratory Therapy Device is a novel device that uses interactive gaming to encourage patient compliance with their prescribed respiratory therapy routines. The device consists of a computer game controller with mouthpiece containing a breath flow sensor that connects to a tablet. With the Jamboxx respiratory therapy device, users can choose from a suite of breath controlled respiratory therapy games to guide them through their routines while receiving real-time feedback, and long-term progress tracking.
Intervention Type
Device
Intervention Name(s)
Jamboxx Musical Device
Intervention Description
Jamboxx musical device is a hands free, breath controlled music device designed for people with quadriplegia. It resembles a common harmonica in that the user slides a mouthpiece along its horizontal axis to change the pitch of the instrument. The device connects to a personal computer via a mini USB to USB cable to interface with software that provides visual feedback for playing notes and sends the information to the computer speakers. The mouthpiece acts as a transducer, changing air pressure created by the user's lungs to a joystick signal to the computer via a differential pressure sensor. The Jamboxx musical device can produce musical sounds of many instruments (trumpet, drums, etc.) in many different scales and in any key
Primary Outcome Measure Information:
Title
Change in Self-Reported Patient Dyspnea
Description
Change in patient reported measure of breathlessness during daily activities from baseline over the course of the 1 year study
Time Frame
reported 1x/ week for the duration of the 1 year study
Secondary Outcome Measure Information:
Title
Multidimensional Dyspnea Profile
Description
A measure of breathlessness after performing an activity
Time Frame
reported 1x/ week for the duration of the 1 year study
Title
Dyspnea-12 Questionnaire
Description
A survey that measures recent breathlessness with 12 questions related to dyspnea, each evaluated on a scale of 0-4 (0=none, 1=mild, 2=moderate, 3=severe) that indicate how troubled people are by each of these 12 topics, for a total possible score ranging from 0 to 36, where lower scores relate to better outcomes.
Time Frame
Months 0, 3, 6, 9, 12
Title
FEV1
Description
measure of pulmonary function (Forced Expiratory Volume over 1 second) measured in liters
Time Frame
Months 0, 3, 6, 9, 12
Title
FVC
Description
measure of pulmonary function (Forced Vital Capacity) measured in liters
Time Frame
Months 0, 3, 6, 9, 12
Title
PEF
Description
measure of pulmonary function (Peak Expiratory Flow) measured in liters
Time Frame
Months 0, 3, 6, 9, 12
Title
MEP
Description
measure of pulmonary function (Maximum Expiratory Pressure) measured in centimeters of H2O
Time Frame
Months 0, 3, 6, 9, 12
Title
MIP
Description
measure of pulmonary function (maximum inspiratory pressure) measured in centimeters of H2O
Time Frame
Months 0, 3, 6, 9, 12
Title
Device usability
Description
Measurement of enjoyment and engagement with the intervention via survey
Time Frame
Months 6, 12
Title
Clinically relevant events
Description
e.g. patient being sent for a chest x-ray, being ordered chest physiotherapy or blood tests
Time Frame
Months 0, 3, 6, 9, 12
Title
Patient Empowerment
Description
Measured via a single question ranked on a likert scale: "I believe that this respiratory therapy empowered me to protect my breathing" With answer options of 1. strongly disagree, 2. disagree, 3. neutral, 4. agree, 5. strongly agree, with higher numbers corresponding to better outcomes
Time Frame
Months 0, 3, 6, 9, 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Quadriplegic and other spinal cord injury outpatients will be included. Exclusion Criteria: Individuals already adhering to a daily regimen of prescribed respiratory therapy routine will be excluded.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marilyn Fisher, MD
Organizational Affiliation
Albany Medical College
Official's Role
Study Chair
Facility Information:
Facility Name
Albany Medical Center
City
Albany
State/Province
New York
ZIP/Postal Code
12208
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Effectiveness of Jamboxx Respiratory Therapy Device: Study 1

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