Trial of Asthma Self-Management Education in Patients With Depressive Symptoms

Not Applicable

Completed

• Conditions: Asthma; Depression; Anxiety
• Interventions: Behavioral: Asthma self-management

• Registration Number: NCT01708070
• Lead Sponsor: Hospital for Special Surgery, New York

Brief Summary

Although depressive and anxious symptoms are common in asthma patients and are associated with worse clinical and resource utilization outcomes, there have been no studies focusing on the particular challenges of improving asthma self-management in this population. The investigators hypothesize that a tailored intervention to improve asthma self-management in patients with a known history of depressive and anxious symptoms will be effective in improving asthma-related quality of life.

Detailed Description

Depressive and anxious conditions are common during the lifetime of asthma patients and have been shown to be associated with worse asthma as defined by more symptoms, more hospitalizations and greater use of medications. There have been few studies trying to improve asthma outcomes in patients with known depression. One method to improve outcomes is to instruct patients in ways to better self manage asthma. The goal of this study is to test a comprehensive intervention to improve asthma self-management by increasing knowledge and self-efficacy in patients with a known history of a positive screen for depression. Patients will be randomized to two groups - a control group and an intervention group. Patients in the control group will receive an asthma workbook, will make a contract to adopt behaviors they think will improve asthma, and will receive telephone follow-ups approximately every week for 8 weeks and then approximately every 2 months. Patients in the intervention group will receive these components plus they will be taught how to use a peak flow meter and specific chapters of the workbook will be used as templates for focused instruction during telephone follow-ups. The primary outcome will be a comparison of within-patient change in asthma-related quality of life between groups.

Study Timeline

• Study Start: 2012-10
• Study First Submitted: 2012-10-11
• Study First Submitted QC: 2012-10-15
• Study First Posted: 2012-10-16
• Primary Completion: 2016-05
• Study Completion: 2016-05
• Status Verified: 2016-09
• Last Update Submitted: 2016-09-09
• Last Update Posted: 2016-09-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 66

Inclusion Criteria

• 18 years of age or older
• known history of depressive or anxious symptoms

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Exclusion Criteria

• pregnant
• has cognitive deficits
• no access to telephone

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Asthma self-management control	Asthma self-management	The control state will involve a self-management workbook and contracting to improve self-management behaviors.
Asthma self-management experimental	Asthma self-management	The intervention will involve a self-management workbook, contracting to improve self-management behaviors, instruction in using of a peak flow meter, and follow-up discussions based on the workbook.

Primary Outcome Measures

Name	Time	Method
Change in asthma-related quality of life	Approximately 12 months	The primary outcome will be a comparison of within-patient change in Asthma Quality of Life Questionnaire scores between groups.

Secondary Outcome Measures

Name	Time	Method
Number of urgent resource utilization visits for asthma	Approximately 12 months	An additional outcome will be the comparison of the number or urgent resource utilization visits for asthma.

Trial Locations

Locations (1)

Weill Cornell Internal Medicine Associates/Hospital for Special Surgery; 🇺🇸 New York, New York, United States