Evaluating Efficacy of Smart Device in Assisting With Inhaler Technique and Adherence (MOMMIASTHMA1)
Primary Purpose
Asthma, Adherence, Medication, Childhood Asthma
Status
Unknown status
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
CapMedic smart inhaler device
Video-based guidance
Sponsored by
About this trial
This is an interventional supportive care trial for Asthma
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of Asthma
- Regular user of MDI
- Asthma Control Test (ACT) scores between 15 and 25
- FEV1 between 60-80% of predicted (persistent mild-moderate)
- Disease severity in the range mild-moderate
- Access to a Smartphone and internet during the entire duration of the study.
- Cognitively able to utilize the device and express interest in participating.
Exclusion Criteria:
- Patients without asthma
- With developmental disabilities
- Do not speak English
- Do not own a Smartphone
Sites / Locations
- Pediatric Diagnostic CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Control Group
Treatment Group
Arm Description
In this arm, patients are provided with standard-of-care instructions on using MDIs correctly and regularly at home. The MDI usage is recorded using CapMedic device with active guidance turned off.
In this arm, patients are provided with active guidance from CapMedic device on using MDIs correctly and regularly at home. The MDI usage is recorded using CapMedic device with active guidance turned on.
Outcomes
Primary Outcome Measures
MDI use Competence in Clinic
Correctness of Inhaler Use measured using CapMedic device during recruitment. Competence is measured as a score out of 4 for 4 steps of MDI use: 1. Shaking, 2. Orientation, 3. Coordination 4. Duration of inhalation
MDI use Competence at home
Correctness of Inhaler Use measured using CapMedic device at home. Competence is measured as a score out of 4 for 4 steps of MDI use: 1. Shaking, 2. Orientation, 3. Coordination 4. Duration of inhalation
Secondary Outcome Measures
PEF Lung Function in Clinic
PEF measured using CapMedic device during recruitment. PEF is measured in L/min.
FEV1 Lung Function in Clinic
FEV1 measured using CapMedic device during recruitment. FEV1 is measured in L.
PEF Lung Function at home
PEF measured using CapMedic device at home. PEF is measured in L/min.
FEV1 Lung Function at home
FEV1 measured using CapMedic device at home. FEV1 is measured in L.
MDI use Adherence
Regularity of MDI use measured by CapMedic device at home, measured as a % of puffs taken per week compared to prescribed dosage.
Full Information
NCT ID
NCT04250779
First Posted
January 29, 2020
Last Updated
September 13, 2020
Sponsor
Landon Pediatric Foundation
Collaborators
Cognita Labs LLC
1. Study Identification
Unique Protocol Identification Number
NCT04250779
Brief Title
Evaluating Efficacy of Smart Device in Assisting With Inhaler Technique and Adherence
Acronym
MOMMIASTHMA1
Official Title
Evaluating Efficacy of Smart Device in Assisting With Inhaler Technique and Adherence
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
July 1, 2019 (Actual)
Primary Completion Date
July 1, 2021 (Anticipated)
Study Completion Date
December 1, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Landon Pediatric Foundation
Collaborators
Cognita Labs LLC
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
No
5. Study Description
Brief Summary
Asthma affects over 10 million children in the U.S., and poses a significant health and cost burden. Metered dose inhaler (MDI) is the most common method of treatment. Studies show that up to 80% of patients demonstrate incorrect use of MDIs, which results in suboptimal medication delivery to the lungs.
Asthma control can be followed by symptoms, rescue medication usage and measures of airflow obstruction. Current options to monitor control include an asthma diary (relies on consistent use by the patient), pharmacy records of medication dispensing (dispensing does not equal usage), and peak expiratory flow (PEF) meters (significant variability in technique leading to inconsistent results).
CapMedic is a smart inhaler and home spirometer device which aims to assist with correct MDI usage and to monitor asthma control. CapMedic fits on top of the MDI inhaler and provides live audio-visual-haptic cues to guide the patient for correctly using their inhaler. CapMedic includes a built-in forced expiratory flow in 1 second (FEV1, a measure of airflow) and PEF meter. It will utilize the same audio-visual-haptic hardware to implement live cues that encourage patient's effort in performing accurate at-home FEV1/PEF test. Cap will also be able to log medication usage and Medic application will allow patients to keep an asthma symptom diary.
Detailed Description
CapMedic is a smart inhaler and home spirometer device which aims to assist with correct MDI usage and to monitor asthma control. CapMedic fits on top of the MDI inhaler and provides live audio-visual-haptic cues to guide the patient for correctly using their inhaler. CapMedic includes a built-in forced expiratory flow in 1 second (FEV1, a measure of airflow) and PEF meter. It will utilize the same audio-visual-haptic hardware to implement live cues that encourage patient's effort in performing accurate at-home FEV1/PEF test. Cap will also be able to log medication usage and Medic application will allow patients to keep an asthma symptom diary.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma, Adherence, Medication, Childhood Asthma
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Research will initially involve collection of data describing the participants' current use of their medication following standard education. Subsequent phases will add audio / haptic coaching to the process of administering medication by MDI, and follow the same participants to determine whether or not there is improvement in technique and adherence to therapy.
The device will be used with a placebo inhaler (given AFTER the participant's regular medication is taken by standard techniques), to determine how participants use the device, and to identify the most effective coaching interventions for this age group. This is to ensure that the device does not interfere with delivery of routine asthma controller medications. The data will be used to develop a subsequent, longer term study in which we will evaluate the effect of the coaching device on asthma control, when it is used with the subject's controller medication.
Masking
Participant
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control Group
Arm Type
Placebo Comparator
Arm Description
In this arm, patients are provided with standard-of-care instructions on using MDIs correctly and regularly at home. The MDI usage is recorded using CapMedic device with active guidance turned off.
Arm Title
Treatment Group
Arm Type
Active Comparator
Arm Description
In this arm, patients are provided with active guidance from CapMedic device on using MDIs correctly and regularly at home. The MDI usage is recorded using CapMedic device with active guidance turned on.
Intervention Type
Device
Intervention Name(s)
CapMedic smart inhaler device
Intervention Description
The CapMedic device provides active coaching to promote correct and regular use of MDI.
Intervention Type
Behavioral
Intervention Name(s)
Video-based guidance
Intervention Description
Patients are shown a video of how to use inhalers correctly and any questions are answered by the clinician. They are also encouraged to use inhalers regularly and correctly at home.
Primary Outcome Measure Information:
Title
MDI use Competence in Clinic
Description
Correctness of Inhaler Use measured using CapMedic device during recruitment. Competence is measured as a score out of 4 for 4 steps of MDI use: 1. Shaking, 2. Orientation, 3. Coordination 4. Duration of inhalation
Time Frame
1 day
Title
MDI use Competence at home
Description
Correctness of Inhaler Use measured using CapMedic device at home. Competence is measured as a score out of 4 for 4 steps of MDI use: 1. Shaking, 2. Orientation, 3. Coordination 4. Duration of inhalation
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
PEF Lung Function in Clinic
Description
PEF measured using CapMedic device during recruitment. PEF is measured in L/min.
Time Frame
1 day
Title
FEV1 Lung Function in Clinic
Description
FEV1 measured using CapMedic device during recruitment. FEV1 is measured in L.
Time Frame
1 day
Title
PEF Lung Function at home
Description
PEF measured using CapMedic device at home. PEF is measured in L/min.
Time Frame
8 weeks
Title
FEV1 Lung Function at home
Description
FEV1 measured using CapMedic device at home. FEV1 is measured in L.
Time Frame
8 weeks
Title
MDI use Adherence
Description
Regularity of MDI use measured by CapMedic device at home, measured as a % of puffs taken per week compared to prescribed dosage.
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of Asthma
Regular user of MDI
Asthma Control Test (ACT) scores between 15 and 25
FEV1 between 60-80% of predicted (persistent mild-moderate)
Disease severity in the range mild-moderate
Access to a Smartphone and internet during the entire duration of the study.
Cognitively able to utilize the device and express interest in participating.
Exclusion Criteria:
Patients without asthma
With developmental disabilities
Do not speak English
Do not own a Smartphone
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chris Landon, M.D.
Phone
8053401366
Email
chris.landon@ventura.org
First Name & Middle Initial & Last Name or Official Title & Degree
Emilie Paronyan
Phone
8184393664
Email
emilieparonyann@gmail.com
Facility Information:
Facility Name
Pediatric Diagnostic Center
City
Ventura
State/Province
California
ZIP/Postal Code
93003
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chris Landon, MD
Phone
805-641-4490
Email
chris.landon@ventura.org
First Name & Middle Initial & Last Name & Degree
Chris Landon, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
35691614
Citation
Chan A, De Simoni A, Wileman V, Holliday L, Newby CJ, Chisari C, Ali S, Zhu N, Padakanti P, Pinprachanan V, Ting V, Griffiths CJ. Digital interventions to improve adherence to maintenance medication in asthma. Cochrane Database Syst Rev. 2022 Jun 13;6(6):CD013030. doi: 10.1002/14651858.CD013030.pub2.
Results Reference
derived
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Evaluating Efficacy of Smart Device in Assisting With Inhaler Technique and Adherence
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