Skip to content

Cornell Translational Behavioral Science Research Consortium: Asthma Qualitative Study

Cornell Translational Behavioral Science Research Consortium: Asthma Qualitative Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00195065
Enrollment
60
Registered
2005-09-19
Start date
2003-04-30
Completion date
2003-09-30
Last updated
2008-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

Asthma, Behavior change, Physical activity, Risk reduction

Brief summary

To explore and illuminate the cultural, social, and psychological factors that either facilitate or serve as barriers to behavioral change in asthma patients.

Detailed description

1. Through a series of open-ended questions we will explore and build a better understanding of how different patient populations view asthma and the difficulties they face in changing behavior. In addition the responses to such questions should help us to better understand and anticipate some of the barriers and issues that participants may face in successfully changing their behaviors. 2. The second objective is to use the responses obtained to inform how an intervention of positive affect induction and self-affirmation should be operationalized and tailored.

Interventions

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients will be eligible for this study if their physicians consider them medically able to participate, if they are 18 years of age or older, and if they have a diagnosis of mild to moderate asthma based on the NHLBI Asthma Expert Panel's classification system which rates symptoms, frequency of exacerbations, nocturnal attacks, activity restriction, use of medications, and pulmonary function.

Exclusion criteria

Patients will be excluded from this study for the following reasons: * If they are unable to walk several blocks for whatever reason; * If they have musculoskeletal or neurological deficits that preclude increased physical activity; * If they have other pulmonary diseases; * If they have cardiac disease or other severe comorbidity; * If they are unable to provide informed consent because of cognitive deficits; * If they refuse to participate.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026