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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00767845
Other study ID # CDR0000600455
Secondary ID BCM-H-19323
Status Withdrawn
Phase N/A
First received October 4, 2008
Last updated November 7, 2016
Start date June 2006
Est. completion date May 2008

Study information

Verified date November 2016
Source Baylor College of Medicine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

RATIONALE: Gathering information about symptom management from patients with localized prostate cancer may help doctors improve patients' quality of life.

PURPOSE: This clinical trial is studying symptom management in African-American men with localized prostate cancer.


Description:

OBJECTIVES:

- Develop a symptom management intervention for African-American men treated for localized prostate cancer, with a particular emphasis on low health literacy men.

OUTLINE: Participants are interviewed by the principal investigator over the phone or meet the principal investigator at the Veterans Administration prostate cancer clinic. If the interview is conducted in the clinic, it is held in a private room in the clinic.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date May 2008
Est. primary completion date May 2008
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 120 Years
Eligibility DISEASE CHARACTERISTICS:

- Biopsy-proven localized prostate cancer

- Has received treatment for prostate cancer

- Patient self-identifies as being of African-American descent

PATIENT CHARACTERISTICS:

- Able to speak and read in English

- Has an address in order to receive study materials by mail (a street address or post office box)

- Has either a telephone in order to be interviewed OR is able to meet the principal investigator at the Veterans Administration prostate clinic and be interviewed there

PRIOR CONCURRENT THERAPY:

- See Disease Characteristics

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Other:
questionnaire/survey administration


Locations

Country Name City State
United States Dan L. Duncan Cancer Center at Baylor College of Medicine Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
Baylor College of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Symptom management taxonomy
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