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Telehealth Technology for Asthma Management
N/A
Waitlist Available
Led By Chris Carlsten, M.D.
Research Sponsored by University of British Columbia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Must have moderate or severe asthma
Must be capable to communicate in English or French
Must not have
Patients with chronic obstructive pulmonary disease (COPD)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at the end of year 3 through year four of the intervention
Awards & highlights
No Placebo-Only Group
Summary
This trial tests a mobile app that helps adults with asthma manage their condition better. The app provides an electronic action plan and sends regular reminders to check asthma control. The goal is to see if this approach reduces asthma attacks and improves overall health.
Who is the study for?
This trial is for adults with moderate or severe asthma who have had at least one exacerbation in the past year, are on both reliever and controller medications, and can use a digital device with internet. They must be able to communicate in English or French but cannot participate if they have COPD.
What is being tested?
The CANATEXTS study tests whether a Telehealth intervention using an electronic asthma action plan (eAAP) via mobile devices, along with educational content and weekly reminders, can reduce asthma exacerbations over 12 months compared to standard written AAPs.
What are the potential side effects?
Since this trial involves non-medical interventions like text messaging and electronic plans rather than drugs, typical medication side effects are not expected. However, participants may experience issues related to technology use.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have moderate or severe asthma.
Select...
I can communicate in English or French.
Select...
I am prescribed both quick-relief and long-term asthma medications.
Select...
I had at least one worsening of my condition in the last year.
Select...
I have been diagnosed with asthma.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have chronic obstructive pulmonary disease (COPD).
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ at the end of year 3 through year four of the intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at the end of year 3 through year four of the intervention
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Exacerbation
Secondary study objectives
Asthma control
Medication adherence
Other study objectives
Cost effectiveness
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention groupExperimental Treatment1 Intervention
Intervention group/telehealth Arm: will be provided access to their electronic asthma action plan (eAAP) via a web Uniform Resource Locator (URL), receive weekly short message service (SMS) check-ins for one year, and be able to communicate with the site's research coordinator (RC) and Certified Respiratory Educator (CRE) via an integrated and interactive (two-way) SMS feature to manage their asthma
Group II: Control groupActive Control1 Intervention
Control group/standard care Arm: will receive their written Asthma Action Plan (wAAP) and information on how to use it by the site's Certified Respiratory Educator to manage their asthma
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for asthma include inhaled corticosteroids, which reduce inflammation in the airways, and beta agonists, which relax the muscles around the airways to improve airflow. Combination therapies, such as inhaled corticosteroids with long-acting beta agonists, provide both anti-inflammatory and bronchodilator effects.
The CANATEXTS trial emphasizes the use of an electronic asthma action plan (eAAP), disease-related education, and weekly SMS reminders to enhance self-management. This approach helps patients adhere to their treatment plans, recognize early signs of exacerbations, and take appropriate actions, ultimately improving asthma control and reducing the risk of severe exacerbations.
Combination formoterol and budesonide as maintenance and reliever therapy versus current best practice (including inhaled steroid maintenance), for chronic asthma in adults and children.
Combination formoterol and budesonide as maintenance and reliever therapy versus current best practice (including inhaled steroid maintenance), for chronic asthma in adults and children.
Find a Location
Who is running the clinical trial?
Vancouver Coastal Health Research InstituteOTHER
26 Previous Clinical Trials
4,570 Total Patients Enrolled
University of British ColumbiaLead Sponsor
1,472 Previous Clinical Trials
2,489,000 Total Patients Enrolled
16 Trials studying Asthma
3,176 Patients Enrolled for Asthma
Chris Carlsten, M.D.Principal InvestigatorUniversity of British Columbia
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have moderate or severe asthma.I can communicate in English or French.I am prescribed both quick-relief and long-term asthma medications.I had at least one worsening of my condition in the last year.I have been diagnosed with asthma.I have chronic obstructive pulmonary disease (COPD).
Research Study Groups:
This trial has the following groups:- Group 1: Intervention group
- Group 2: Control group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.