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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
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at the end of year 3 through year four of the intervention
Awards & highlights
Study Summary
This trial will assess the effectiveness of an electronic asthma action plan (eAAP) on mobile devices, compared to a written asthma action plan (wAAP), on asthma outcomes in a Canada-wide study.
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.Check my eligibility
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.See study design
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.
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
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Exacerbation
Secondary outcome measures
Asthma control
Medication adherence
Other outcome measures
Cost effectiveness
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
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
1,415 Previous Clinical Trials
2,466,396 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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are participants aged 50 and above eligible to join this trial?
"To be considered for enrollment, patients must fall between 19 and 80 years of age."
Answered by AI
Is there an ongoing recruitment process for this experiment?
"Clinicaltrials.gov shows that this trial, first posted on March 1st 2023, is no longer recruiting participants. However, 639 other medical studies are currently enrolling patients for their respective trials."
Answered by AI
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