Developing Asthma Interventions Using Community Based Research

Asthma Clinical Trial

Official title:

Feasibility of Developing an Effective Asthma Intervention Using CBPR Methods

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00728169
• Other study ID #: 020715JEM13314
• Secondary ID: P20RR011792
• Status: Completed
• Phase: N/A
• First received: July 31, 2008
• Last updated: September 17, 2009
• Start date: July 2008
• Est. completion date: July 2009

Study information

• Verified date: September 2009
• Source: Meharry Medical College
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 62
• Est. completion date: July 2009
• Est. primary completion date: July 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Self-identified African-American, 18 yrs. or older, resident of Davidson County, Tennessee at least 1 year.

Exclusion Criteria:

• Under 18 yrs. of age

• Non-African American

• Non-English speaking

• Do not reside in Davidson County, Tennessee

Study Design

Observational Model: Ecologic or Community, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Asthma

Locations

Country	Name	City	State
United States	Meharry Medical College	Nashville	Tennessee

Sponsors (1)

Lead Sponsor	Collaborator
Meharry Medical College

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Use information from Community Based Participatory Research to develop an intervention to improve asthma self management behaviors.		2 years	No