Self-regulation for Older Adults With Asthma Through Remote Education
NCT ID: NCT05722834
Last Updated: 2024-07-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
20 participants
INTERVENTIONAL
2023-06-13
2024-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The purpose of this study is to implement and evaluate an asthma self-management intervention through multiple locations in the United States that is tailored to the challenges older adults face and is based on an individual behavioral theory of change.
Eligible participants will be enrolled and participate for six weeks in the SOAR intervention.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Asthma Self-Management in Older Adults
NCT00941694
Achieving Better Control for Older Adults With Asthma
NCT01979055
A Randomized Trial to Improve Quality of Life Outcomes in Asthma Patients
NCT00197964
The Effect of Self-regulatory Education on Women With Asthma
NCT00217802
Rural Asthma Effectiveness Study
NCT03533764
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.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
SOAR intervention
The SOAR intervention will be a remote intervention that will follow a self-regulation process in which the participant first selects a specific problem to address and researches how asthma is preventing resolution of the problem, and finally identifies and develops a plan to achieve the objective.
SOAR intervention
This program intervention will be over 6 weeks and participants will have two group sessions and individual sessions, all conducted by an asthma health coach over Zoom (or phone). The two Zoom group sessions will be recorded so that all the information from the conversations will be maintained and used for research purposes. Additionally, participants will keep track of asthma symptoms and complete surveys at specified time-points (the last one at 6 months after participation).
Primary care physicians will be sent emails regarding the self-management goals of their patients.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
SOAR intervention
This program intervention will be over 6 weeks and participants will have two group sessions and individual sessions, all conducted by an asthma health coach over Zoom (or phone). The two Zoom group sessions will be recorded so that all the information from the conversations will be maintained and used for research purposes. Additionally, participants will keep track of asthma symptoms and complete surveys at specified time-points (the last one at 6 months after participation).
Primary care physicians will be sent emails regarding the self-management goals of their patients.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Poorly controlled asthma, as evidenced by a score ≤ 19 on the Asthma Control Test
* Have a primary care provider willing to participate in the study by receiving email updates regarding the status of the participant
Exclusion Criteria
* A greater than 20 pack-year smoking history
* Lack of telephone access
* Decreased cognitive capacity such that participation in the program would not be possible
60 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
American Lung Association
OTHER
University of Michigan
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Alan Baptist
Associate Professor of Internal Medicine
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Alan Baptist, MD
Role: PRINCIPAL_INVESTIGATOR
University of Michigan
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Illinois-Chicago
Chicago, Illinois, United States
University of Michigan
Ann Arbor, Michigan, United States
University of Vermont
Burlington, Vermont, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
HUM00219528
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.