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A mHealth Intervention to Improve Symptom Control in Children and Adolescents With Difficult-to-control Asthma

Primary Purpose

Asthma in Children

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Happyair Ecosystem
Sponsored by
Raquel Sebio
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Asthma in Children

Eligibility Criteria

6 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • children between 6 and 18 years old;
  • diagnosis of moderate to severe persistent asthma according to the international guidelines
  • difficult to control asthma according to a scoring in the Asthma Control Questionnaire (ACQ) of 1.5 points;
  • access to internet and a smartphone, tablet or computer;
  • ability to understand and use the web-based platform (in children <12 years the ability of the tutor or legal guardian);
  • informed consent (by the tutor or legal guardian)

Exclusion Criteria:

  • patients who have had an exacerbation in the previous two weeks;
  • patients with intermittent asthma and/or well-controlled asthma according to the ACQ score of <1.5;
  • any neurological or psychiatric condition that prevents patients to use adequately the platform.

Sites / Locations

  • Hospital Universitari Parc TaulíRecruiting
  • Hospital del MarRecruiting
  • Hospital Universitari Vall d'HebronRecruiting
  • Hospital Santa Creu i Sant PauRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention Group

Control Group

Arm Description

Participants in the IG will be given free access to the HappyAir platform during a 6-month period. This platform combines online/offline content to help patients with chronic respiratory diseases monitor their symptoms and improve self-management. In addition to tailored information on their condition, participants will be encouraged to fill in daily data on their physical activity levels, symptomatology, use of rescue medication and mood. In children under 12 years, parents or caregivers will fill in this information. Patients will be asked to record their peak expiratory flow using an electronic peak flow meter twice daily and to fulfil the Asthma Control Questionnaire once a week. They will also have a device connected to their inhaler to record adherence to the medical treatment and will get daily reminders in their smartphones. Every patient will be assigned a respiratory coach who will monitor patient during the study and whom the patients can contact at any time.

Subjects in the CG will receive standard care consisting of periodic visitations at the Allergology or Paediatric Pulmonology Unit in their respective hospitals every 4 - 8 weeks according to their physician's criteria. In addition, patients and caregivers in both groups will receive one educational session regarding the correct use of their inhalers.

Outcomes

Primary Outcome Measures

Differences in asthma control inter-group
We will assess differences in asthma control (score) according to the Asthma Control Questionnaire (ACQ) in comparison with the control group. The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Differences in asthma control inter-group
We will assess differences in asthma control (score) according to the Asthma Control Questionnaire (ACQ) in comparison with the control group. The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.

Secondary Outcome Measures

Changes in asthma control intra-group for the intervention group
Changes in asthma control (score) according to the Asthma Control Questionnaire pre to post-intervention (Intervention Group). The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Changes in asthma control intra-group for the intervention group
Changes in asthma control (score) according to the Asthma Control Questionnaire at follow-up (Intervention Group). The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Changes in asthma control intra-group for the control group
Changes in asthma control (score) according to the Asthma Control Questionnaire post-intervention (Control Group). The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Changes in asthma control intra-group for the control group
Changes in asthma control (score) according to the Asthma Control Questionnaire pre to post-intervention (Control Group). The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Inclusion rates (feasibility)
Total number of patients recruited which consented from those eligible
Completion rates
Total number of patients who completed the interventions from those who were recruited
Incidence of exacerbations
Number of exacerbations (events) in a year in both groups. Exacerbations will be defined as any worsening in asthma symptoms that requires an increase in the usual therapy, an unscheduled physician visit, treatment in the emergency room or hospitalization.

Full Information

First Posted
November 13, 2019
Last Updated
August 31, 2021
Sponsor
Raquel Sebio
Collaborators
Hospital Vall d'Hebron, Hospital Santa Creu i Sant Pau, Hospital Universitari Parc Taulí, Hospital Universitari Parc Salut Mar
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1. Study Identification

Unique Protocol Identification Number
NCT04166344
Brief Title
A mHealth Intervention to Improve Symptom Control in Children and Adolescents With Difficult-to-control Asthma
Official Title
Effectiveness of a Web-based, Digital Health Platform Combining Social Care and Respiratory Coach Support to Improve Adherence to Treatment and Symptom Control in Children and Adolescents With Difficult-to-control Asthma
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
September 1, 2022 (Anticipated)
Study Completion Date
September 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Raquel Sebio
Collaborators
Hospital Vall d'Hebron, Hospital Santa Creu i Sant Pau, Hospital Universitari Parc Taulí, Hospital Universitari Parc Salut Mar

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Asthma is the most common chronic respiratory disease worldwide. Despite advances in asthma management, control of the disease is still a challenge especially among children. Information and communications technology (ICT) have been recently used in clinical practice to increase awareness of diseases, encourage patients to engage in the management of their conditions and improve monitoring and surveillance. The investigators of this study will test a new digital platform combining online/offline content aimed to improve asthma control and reduce exacerbations and unnecessary consultations in children with difficult-to-control asthma. A randomised controlled trial enrolling 60 patients allocated in two groups has been designed. The intervention group (IG) will be granted free access during 6 months to a web-based platform. During this period, patient will have access to online/off line content to improve disease awareness, monitor signs and symptoms and will also get the support of a respiratory coach. In addition, patients in this group will receive an electronic peak flow meter to register daily variations in maximal expiratory flow and an electronic device to connect to their inhaler to track adequate intake of inhaled medication. The control group (CG) will receive usual care consisted of scheduled visitations to medical doctors every 4 - 8 weeks. Both groups will be evaluated at baseline, post-intervention (6 months) and at follow up (one year) in the following variables: age, gender, asthma severity classification according to international guidelines, date of diagnosis, weight, height, Body Mass Index (BMI), forced expiratory volume in 1 second (FEV1), Asthma Control Questionnaire score, treatment received for asthma, number of exacerbations in the previous 6 months and concomitant diseases. Exacerbations will be defined as any worsening in asthma symptoms that requires an increase in the usual therapy, an unscheduled physician visit, treatment in the emergency room or hospitalization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma in Children

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
Participants in the IG will be given free access to the HappyAir platform during a 6-month period. This platform combines online/offline content to help patients with chronic respiratory diseases monitor their symptoms and improve self-management. In addition to tailored information on their condition, participants will be encouraged to fill in daily data on their physical activity levels, symptomatology, use of rescue medication and mood. In children under 12 years, parents or caregivers will fill in this information. Patients will be asked to record their peak expiratory flow using an electronic peak flow meter twice daily and to fulfil the Asthma Control Questionnaire once a week. They will also have a device connected to their inhaler to record adherence to the medical treatment and will get daily reminders in their smartphones. Every patient will be assigned a respiratory coach who will monitor patient during the study and whom the patients can contact at any time.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Subjects in the CG will receive standard care consisting of periodic visitations at the Allergology or Paediatric Pulmonology Unit in their respective hospitals every 4 - 8 weeks according to their physician's criteria. In addition, patients and caregivers in both groups will receive one educational session regarding the correct use of their inhalers.
Intervention Type
Behavioral
Intervention Name(s)
Happyair Ecosystem
Intervention Description
Happyair Ecosystem is a Smart Community for the integral care of patients with chronic or rare respiratory diseases such as Asthma, COPD or Alfa-1. Our community provides online & offline training and resources in digital health and social care to patients, family, caregivers, healthcare professionals and researchers. Using our platform, all of our members will be able to connect in order to improve the health and well-being of patients, learn to manage self-care, ensure an active lifestyle, and contribute to the development of current and future research projects.
Primary Outcome Measure Information:
Title
Differences in asthma control inter-group
Description
We will assess differences in asthma control (score) according to the Asthma Control Questionnaire (ACQ) in comparison with the control group. The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Time Frame
6 months
Title
Differences in asthma control inter-group
Description
We will assess differences in asthma control (score) according to the Asthma Control Questionnaire (ACQ) in comparison with the control group. The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Changes in asthma control intra-group for the intervention group
Description
Changes in asthma control (score) according to the Asthma Control Questionnaire pre to post-intervention (Intervention Group). The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Time Frame
6 months
Title
Changes in asthma control intra-group for the intervention group
Description
Changes in asthma control (score) according to the Asthma Control Questionnaire at follow-up (Intervention Group). The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Time Frame
12 months
Title
Changes in asthma control intra-group for the control group
Description
Changes in asthma control (score) according to the Asthma Control Questionnaire post-intervention (Control Group). The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Time Frame
6 months
Title
Changes in asthma control intra-group for the control group
Description
Changes in asthma control (score) according to the Asthma Control Questionnaire pre to post-intervention (Control Group). The ACQ consists of seven items that are rated according to a seven-point scale where where 0 means no impairment and 6 indicates maximum impairment.
Time Frame
12 months
Title
Inclusion rates (feasibility)
Description
Total number of patients recruited which consented from those eligible
Time Frame
Baseline
Title
Completion rates
Description
Total number of patients who completed the interventions from those who were recruited
Time Frame
12 months
Title
Incidence of exacerbations
Description
Number of exacerbations (events) in a year in both groups. Exacerbations will be defined as any worsening in asthma symptoms that requires an increase in the usual therapy, an unscheduled physician visit, treatment in the emergency room or hospitalization.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: children between 6 and 18 years old; diagnosis of moderate to severe persistent asthma according to the international guidelines difficult to control asthma according to a scoring in the Asthma Control Questionnaire (ACQ) of 1.5 points; access to internet and a smartphone, tablet or computer; ability to understand and use the web-based platform (in children <12 years the ability of the tutor or legal guardian); informed consent (by the tutor or legal guardian) Exclusion Criteria: patients who have had an exacerbation in the previous two weeks; patients with intermittent asthma and/or well-controlled asthma according to the ACQ score of <1.5; any neurological or psychiatric condition that prevents patients to use adequately the platform.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Raquel Sebio-Garcia, PhD
Phone
+34679336288
Email
raquelsebio@lovexair.com
First Name & Middle Initial & Last Name or Official Title & Degree
Inés De Mir-Messa, PhD
Phone
+34619601782
Email
idemir@vhebron.net
Facility Information:
Facility Name
Hospital Universitari Parc Taulí
City
Sabadell
State/Province
Barcelona
ZIP/Postal Code
08208
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laura Valdesoiro, PhD
Email
lauravaldesoiro@gmail.com
Facility Name
Hospital del Mar
City
Barcelona
ZIP/Postal Code
08003
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aracelia Caballero Rabasco, PhD
Email
MACaballeroRabasco@parcdesalutmar.cat
Facility Name
Hospital Universitari Vall d'Hebron
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Inés De Mir-Messa, PhD
Email
idemir@vhebron.net
First Name & Middle Initial & Last Name & Degree
Maria T Garriga-Baraut, MD
Facility Name
Hospital Santa Creu i Sant Pau
City
Barcelona
ZIP/Postal Code
08041
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gemma García del Cerro, MD
Email
GGarciaD@santpau.cat

12. IPD Sharing Statement

Plan to Share IPD
No
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A mHealth Intervention to Improve Symptom Control in Children and Adolescents With Difficult-to-control Asthma

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