Expired Study
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Philadelphia, Pennsylvania 19104


Purpose:

This is a randomized, controlled study that will compare two medication adherence strategies in adults with moderate or severe persistent asthma as a method for improving or maintaining treatment adherence.


Study summary:

Low-income minority adults have excessively high rates of morbidity from asthma. Poor medication adherence has been documented in these individuals and contributes to the high morbidity level. This study will compare a Problem Solving intervention with an Attention Control intervention to improve and sustain asthma self-management in a clinical setting. This study will include strategies to address contextual factors related to adherence. Participants will be recruited from clinics that serve minority and low-income individuals.


Criteria:

Inclusion Criteria: - Receiving treatment for asthma at one of the participating clinics - Moderate or severe persistent asthma according to the NHLBI Guidelines - Current use of prescribed inhaled corticosteroids - Evidence of reversible airflow obstruction, as indicated by the following two criteria: 1. FEV1pp AND less than 80% at the time of study entry or within the 3 years prior to study entry 2. An increase of greater than 15% and 200ml in FEV1 with asthma treatment over the last 3 years (if there is no record of such improvement, participants will be evaluated via spirometry pre- and post-bronchodilator at the first study visit. An increase in FEV1 or FVC greater than 12% and 200 ml in FEV1 30 minutes following albuterol administration will represent evidence of reversible airflow obstruction. If a spirometer is not immediately available, participants may be evaluated using a peak flow meter, which reports a PEF. A PEFpp less than 80% and an improvement of at least 60 L per minute after the administration of albuterol will represent evidence of reversible airflow obstruction) - Has a functional telephone or mobile phone Exclusion Criteria: - Significant lung or cardiac disease (other than hypertension) - Psychiatric illness, such as mania or schizophrenia, that may make it impossible to understand or carry out the Problem Solving intervention


NCT ID:

NCT00115323


Primary Contact:

Study Chair
Andrea Apter
University of Pennsylvania


Backup Contact:

N/A


Location Contact:

Philadelphia, Pennsylvania 19104
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 14, 2017

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