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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06350799
Other study ID # 01741
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 14, 2019
Est. completion date April 28, 2023

Study information

Verified date April 2024
Source VA Puget Sound Health Care System
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

We examined a Community Health Worker (CHW) program for Chronic Obstructive Pulmonary Disease (COPD) in Veteran Participants. The goal of this study was to assess participants' perceived acceptability, appropriateness, and feasibility of the intervention, explore participants' COPD health outcomes, and gather insights from participants and CHWs to inform potential improvements. Veteran participants enrolled in the 12-week intervention and received a series of 9 CHW home, phone, or video visits. These visits provided education and chronic disease self-management practices to improve COPD health. Researchers examined the participant and CHW perception of the intervention through qualitative interviews and surveys.


Description:

Background: One-third of Veterans live in rural areas, and rural patients are more likely to have chronic obstructive pulmonary disease (COPD) and rural Veterans with COPD have lower health status than urban Veterans. COPD patients often have exacerbations that can lead to emergency room visits and hospitalizations. Since COPD exacerbations and hospitalizations can be prevented by interventions such as appropriate use of inhaled COPD medications, focusing efforts to improve COPD management for these high-risk rural Veterans with COPD is essential. Objectives: The proposed project will test the feasibility and potential effectiveness of a Community Health Worker (CHW) intervention to help reduce risk of COPD exacerbations among Veterans. The overall goal of this pilot study is to determine the feasibility and acceptability of a community health worker intervention to promote health behavior change among Veterans with COPD. To target a high risk population, we will focus on Veterans with moderate-severe exacerbations in the past year. Methods: Participants at VA Puget Sound will be enrolled in the study. We will develop a program to serve rural Veterans, though we will also serve all Veterans meeting the criteria particularly in these initial stages at the VA Puget Sound in Seattle. Participants will be scheduled for 9 education visits over 12 weeks that will be delivered either in-person, though a Clinical Video Telehealth into the home (CVT-to-Home), or by phone. Participants will be offered to have additional phone calls in between visits to check-in on their COPD self-management goals and confirm their upcoming appointments. Participants will be followed for a total of 3 months in this pilot study. Data on proportion of eligible patients who enroll in the study, number of intervention visits completed, and completion of study questionnaires will be collected. Data analysis will examine whether any changes in outcomes such as quality of life or physical activity between baseline and follow-up are associated with the intervention. Semi-structured exit interviews will be conducted at the end of the study to assess the design of intervention components, use of technology, appropriateness, and feasibility.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date April 28, 2023
Est. primary completion date May 27, 2021
Accepts healthy volunteers No
Gender All
Age group 45 Years and older
Eligibility Inclusion Criteria: - Clinical diagnosis of COPD - Enrolled in VA primary care - English speaking - Access to a telephone - Clinically stable breathing for at least 1 month prior to enrollment - If available, post-bronchodilator spirometry with FEV1/FVC < 0.70 in the last 5 years - = 1 exacerbation in the past year treated with prednisone and/or antibiotics or treated in the ED or stay in the hospital - Ability to connect to CVT-to-Home Exclusion Criteria: - Nursing home resident or institutionalized - Pregnancy - Pulmonary rehabilitation program in the last year - Uncontrolled hypertension, angina, or heart failure - Life expectancy < 1 year or terminal illness. - Dementia or uncontrolled psychiatric illness - Other safety concerns with participating in physical activity

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States VA Puget Sound Health Care System Seattle Washington

Sponsors (3)

Lead Sponsor Collaborator
VA Puget Sound Health Care System Public Health - Seattle and King County, University of Washington

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Acceptability, Appropriateness, Feasibility Patient perception through interviews one month post-intervention
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