Text2Breathe: Enhance Parent Communication to Reduce Pediatric Asthma Disparities
NCT ID: NCT03032159
Last Updated: 2024-12-03
Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
221 participants
INTERVENTIONAL
2015-08-31
2020-03-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Control Group
Participants randomized to the control group will receive their usual asthma care from their provider. Additionally, participants in the control group will receive reminder texts to schedule with their child's PCP and to get an annual flu shot. Participants will be surveyed over the phone for 20-30 minutes 3, 6, 12, 18, and 24 months after enrollment.
No interventions assigned to this group
Text2Breathe Study Group
The "study" group spends about 10-20 minutes learning about ways to have better communication with their child's primary care provider about his/her asthma. Additionally this group is enrolled in the Text2Breathe messaging program which sends asthma related educational text messages 2 times a week for 3 months. Participants randomized to the study group will also receive reminder texts to schedule with their child's PCP and to get an annual flu shot. Participants will be surveyed over the phone for 20-30 minutes 3, 6, 12, 18, and 24 months after enrollment.
Text2Breathe Study Group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Text2Breathe Study Group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Is the parent of child who is:
* Receiving asthma related care in the emergency department
* 2-12 years old inclusive
* Medicaid insured (no Private insurance)
* Physician diagnosed asthma for at least 12 months
Exclusion Criteria
* Has seen a pulmonary or allergy sub-specialist more than once in the last 6 months
* Has seen a sub-specialist (not pulmonary or allergy) more than once in the last 12 months
* Has been hospitalized for more than 30 days
* Is currently enrolled in another asthma program or study
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
MultiCare Mary Bridge Children's Hospital & Health Center
OTHER
Seattle Children's Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Tumaini Coker
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Tumaini Coker, MD, MBA
Role: PRINCIPAL_INVESTIGATOR
Seattle Children's Hospital and Research Institute
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Seattle Children's
Seattle, Washington, United States
Mary Bridge Children's Hospital at Multi Care Health System
Tacoma, Washington, United States
Countries
Review the countries where the study has at least one active or historical site.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
15488
Identifier Type: -
Identifier Source: org_study_id