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Clinical Trials/NCT02253433
NCT02253433CompletedNot Applicable

The Houston Home-Based Integrated Intervention Targeting Better Asthma Control (HIITBAC) for African Americans

Baylor College of Medicine1 site in 1 country264 target enrollmentStarted: January 8, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
264
Locations
1
Primary Endpoint
Change in Juniper Mini Asthma Quality of Life Questionnaire Score (MiniAQLQ)

Study Overview

Brief Summary

The purpose of this study is to improve the health of African-American adults who have poorly controlled asthma. The study compares a home-based exposure reduction and asthma control intervention to enhanced in-clinic care that includes a standard clinical appointment as well as information from a detailed exposure history, asthma education, assessment for allergies, and a customized asthma self-management plan developed using motivational interviewing. The interventional group receives enhanced in-clinic care, as well as a customized home-based environmental exposure assessment and multicomponent exposure reduction and asthma control intervention (five home visits over approximately 12 months).

Detailed Description

The study hypothesis is that the addition of a holistic, home-based environmental exposure reduction and asthma control intervention to enhanced in-clinic care will result in statistically significant improvements in key measures of health and quality of life among Houston-area African-American adults with poorly controlled asthma.

This is a pragmatic randomized controlled clinical trial that compares the effectiveness of a customized, holistic, patient-centered, home-based environmental intervention for improving asthma control (the "intervention") with enhanced clinic-based care. Both arms receive identical in-clinic care, including collected self-report information from detailed health and exposure questionnaires, asthma education, assessment for allergies, and a customized asthma self-management plan developed using motivational interviewing. The intent of the study is to assess-real-life effectiveness of a home-based intervention in African-American adults with poorly controlled asthma.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •African-American
  • •18 years of age or older
  • •Diagnosis of poorly controlled asthma*
  • •Fixed address within Harris County, Texas, with no intention of moving within the following 12 months
  • •Working telephone number
  • •Verbally fluent in English
  • •Poorly controlled asthma was defined as (1) diagnosed by a physician as having asthma in the past and currently has asthma, and (2) fulfills one or more of the following criteria: (a) one or more emergency department (ED), urgent care visits or hospitalizations for asthma in the preceding year; (b) meets the definition of "very poorly controlled" asthma as defined by the National Asthma Education and Prevention Program, Third Expert Panel on the Diagnosis and Management of Asthma (definition includes daily asthma symptoms, nighttime awakenings two or more times per week, extremely limited normal activity, and/or daily use of a short-acting beta agonist for symptom control); and/or (c) an Asthma Control Test score of 19 or lower.

Exclusion Criteria

  • •Severe co-morbid conditions-such as a poorly controlled psychiatric illness or a condition requiring intense medical treatment that could reasonably be expected to (1) confound the effects of this study's intervention, (2) make it unlikely that a participant could follow the treatment plan, or (3) pose a safety issue for the home-visit team.
  • •A concurrent pulmonary study that could reasonably be expected to confound the effects of the intervention.
  • •Living in a group living facility, such as a nursing home.

Arms & Interventions

Enhanced Clinic Care

Experimental

This arm receives enhanced in-clinic care only.

Intervention: Enhanced Clinic Care (Other)

Enhanced Clinic Care + Home Intervention

Experimental

This arm receives the enhanced in-clinic care intervention, as well as a home-based intervention.

Intervention: Enhanced Clinic Care (Other)

Enhanced Clinic Care + Home Intervention

Experimental

This arm receives the enhanced in-clinic care intervention, as well as a home-based intervention.

Intervention: Enhanced Clinic Care + Home Intervention (Other)

Outcomes

Primary Outcomes

Change in Juniper Mini Asthma Quality of Life Questionnaire Score (MiniAQLQ)

Time Frame: At baseline (enrollment) and exit (approximately 12 mo after enrollment)

Self report. A validated 15-item questionnaire, with each question having seven possible answers score from 1 (worst) to 7 (best). Minimum total score is 15 (worst asthma quality of life). Maximum total score is 105 (best asthma quality of life). By design, an individual's score is reported as the mean (total score/15). Thus the possible mean reported score ranges from 1 (worst asthma quality of life) to 7 (best asthma quality of life).

Change in Asthma Control Test (ACT) Score

Time Frame: At baseline (enrollment) and exit (approximately 12 mo after enrollment)

Self report. The ACT is a validated 5-question scale assessing asthma control over the previous four weeks. Each question has five possible responses, from 1 (worst) to 5 (best). The total score ranges from 5 (worst control) to 25 (best control). In general, a total score of 19 or less suggests poor control.

Secondary Outcomes

  • Change in Emergency Department (ED) Visits for Asthma(At baseline (enrollment) and exit (approximately 12 mo after enrollment))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Winifred J. Hamilton, PhD

Director, Environmental Health Service

Baylor College of Medicine

Study Sites (1)

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