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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00717613
Date of registration: 16/07/2008
Primary sponsor: Baylor College of Medicine
Public title: Psychosocial and Patient Education Needs of Prostate Cancer Patients Selecting Watchful Waiting
Scientific title: Psychosocial and Patient Education Needs of Prostate Cancer Patients Selecting Watchful Waiting
Date of first enrolment: July 2007
Target sample size: 50
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00717613
Study type:  Observational
Study design:  Observational Model: Cohort, Time Perspective: Cross-Sectional  
Countries of recruitment
United States
Contacts
Name:   David M Latini, PhD
Address: 
Telephone:
Email:
Affiliation:  Baylor College of Medicine
Key inclusion & exclusion criteria

Inclusion Criteria:

- 1) male,

- 2) 18 years or older, with biopsy-proven prostate cancer,

- 3) diagnosed with localized disease within the last 24 months,

- 4) have a telephone at the time of enrollment,

- 5) have an address where they can receive study materials by mail (a street address
or post office box),

- 6) able to speak and understand English;

- 7) have selected surveillance, rather than active treatment for his prostate cancer.

Exclusion Criteria:

- 1) female

- 2) no diagnosis of localized prostate cancer

- 3) completed or undergoing active treatment (e.g., surgery, radiotherapy, etc.)

- 4) no phone or US mail address

- 5) unwilling or unable to provide informed consent

- 6) unable to speak and understand English



Age minimum: 18 Years
Age maximum: N/A
Gender: Male
Health Condition(s) or Problem(s) studied
Localized Prostate Cancer
Intervention(s)
Primary Outcome(s)
Health-related quality of life, particularly cancer-specific anxiety and general anxiety [Time Frame: One time retrospective interview]
Secondary Outcome(s)
Secondary ID(s)
DLD2007-01
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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