Skip to main content
Clinical Trials/NCT00769431
NCT00769431
Completed
Not Applicable

FOCUS GROUP EVALUATION OF PROSTATE CANCER SYMPTOM MANAGEMENT EDUCATION MATERIALS

Baylor College of Medicine2 sites in 1 country7 target enrollmentMay 2008
ConditionsProstate Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Baylor College of Medicine
Enrollment
7
Locations
2
Primary Endpoint
Acceptability of the written patient educational materials, in terms of text size, white space, font, and graphics
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

RATIONALE: Collecting feedback from patients with prostate cancer may help doctors develop better symptom management educational materials for patients.

PURPOSE: This clinical trial is evaluating symptom management educational materials for patients with prostate cancer.

Detailed Description

OBJECTIVES: * To collect formative evaluation data about a new educational intervention using focus groups of patients with prostate cancer. * To use the focus group data in the master's research paper of a Baylor College of Medicine physician-assistant student who is documenting the process of organizing and conducting the focus groups, enumerating areas where the new materials are deemed problematic, and identifying themes in the comments made by the focus group participants. OUTLINE: Study participants are assigned to 1 of 3 focus groups according to educational level and ethnicity (i.e., lower educational-level African-American men primarily from the Michael E. DeBakey Veterans Affairs Medical Center (MEDVAMC); lower educational-level Caucasian men from MEDVAMC, Baylor College of Medicine (BCM), or the community; or higher educational-level Caucasian men primarily from BCM or the community). Participants review written patient educational-intervention materials on prostate cancer and provide feedback to the investigator on the content and acceptability of these materials during a 1½-2-hour focus group discussion. Feedback data are used to revise the intervention materials so that they are appropriate to the target population.

Registry
clinicaltrials.gov
Start Date
May 2008
End Date
July 2009
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

David Latini

Assistant Professor

Baylor College of Medicine

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Acceptability of the written patient educational materials, in terms of text size, white space, font, and graphics

Time Frame: Single timepoint

Formative evaluation of the new educational materials, in terms of the comments made by the focus group participants

Time Frame: Single timepoint

Validation that the goals of the educational-intervention instruction are being achieved

Time Frame: Single timepoint

Improvement of the educational-intervention instruction by identification and remediation of problems

Time Frame: Single timepoint

Study Sites (2)

Loading locations...

Similar Trials