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Evaluating Symptom Management Educational Materials for Patients With Prostate Cancer

FOCUS GROUP EVALUATION OF PROSTATE CANCER SYMPTOM MANAGEMENT EDUCATION MATERIALS

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00769431
Enrollment
7
Registered
2008-10-09
Start date
2008-05-31
Completion date
2009-07-31
Last updated
2013-07-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Keywords

stage I prostate cancer, stage IIB prostate cancer, stage IIA prostate cancer

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.

Interventions

OTHEReducational intervention
OTHERstudy of socioeconomic and demographic variables

Sponsors

Baylor College of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Biopsy-proven prostate cancer * Localized disease that has been previously treated * Selected for participation from 1 of the following: * Convenience sample of men from the Baylor College of Medicine (BCM) Urology clinics at Scurlock Tower (including the Urology clinic at MEDVAMC) and local prostate cancer-support groups * Prostate cancer survivors who participated in the US TOO Father's Day Walk/Run or the Gay Pride Celebration PATIENT CHARACTERISTICS: * Able to speak and read in English * Willing to review the written patient educational materials and discuss them in a group setting PRIOR CONCURRENT THERAPY: * See Disease Characteristics

Design outcomes

Primary

MeasureTime frame
Acceptability of the written patient educational materials, in terms of text size, white space, font, and graphicsSingle timepoint
Formative evaluation of the new educational materials, in terms of the comments made by the focus group participantsSingle timepoint
Validation that the goals of the educational-intervention instruction are being achievedSingle timepoint
Improvement of the educational-intervention instruction by identification and remediation of problemsSingle timepoint

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026