Clinical Trials Directory

Trials / Completed

CompletedNCT00728169

Developing Asthma Interventions Using Community Based Research

Feasibility of Developing an Effective Asthma Intervention Using CBPR Methods

Status
Completed
Phase
Study type
Observational
Enrollment
62 (estimated)
Sponsor
Meharry Medical College · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to identify community resources and challenges in improving the health of community members with asthma. The primary goal of this project is to use Community-Based Participatory Research methodology to develop interventions aimed at improving asthma management in high-risk African American asthmatics. This "ground-up" longterm approach has never been tested before in asthmatics. The primary goal of this study will be accomplished with four specific aims: Aim 1. Conduct focus groups to identify barriers to asthma management in the target population. Aim 2. Use a community advisory board (CAB) consisting of participants selected from the various focus groups to gather information about solutions for the above barriers. Aim 3. Use the information from the CAB to develop an intervention to improve asthma self management behaviors in the target population. Aim 4. Refine the developed intervention based on feedback from focus groups conducted in Aim 1.

Detailed description

Volunteer will be asked to respond to several questions that address their perceptions about asthma. Volunteers will also be asked to discuss their beliefs about asthma. Everyone in the group will be given an opportunity to answer questions. Volunteers can decide that they no longer want to participate in the group discussion at any time. The discussion will last from 1.5 - 2 hours. The focus group discussion will have a maximum of 10 people. We will be audio and video taping the discussion so that we do not miss any information that volunteers share with us. The audio and video tapes will not be shared with anyone outside our staff. Volunteer participation in this study is voluntary and there will be no negative consequences if volunteers decide not to participate. Volunteers are also free to withdraw from this study at any time. Withdrawal or refusal to participate will not affect health care services or other rights.

Conditions

Timeline

Start date
2008-07-01
Primary completion
2009-07-01
Completion
2009-07-01
First posted
2008-08-05
Last updated
2009-09-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00728169. Inclusion in this directory is not an endorsement.