Prostate Cancer Clinical Trial
A Survivorship Care Plan and Embedded Navigation Tool
Summary
This is a parallel group, multisite prospective clinical study. The purpose of this study is to evaluate whether ASCENT enables patients to adhere to the survivorship guidelines and improves coordination of care to address patient needs.
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed diagnosis of prostate adenocarcinoma
Age ≥18 years
Receiving curative intent radiotherapy for prostate cancer (Note: post-operative radiotherapy [i.e., "adjuvant" or "salvage radiotherapy subsequent to prostatectomy] is allowed.)
Subjects will be enrolled within two weeks prior to and two weeks after the final fraction of radiotherapy.
Receiving androgen deprivation therapy (ADT) for a duration of ≥3 consecutive months as follows:
GnRH agonist or antagonist (medical castration), with or without an anti-androgen (i.e., bicalutamide, flutamide, nilutamide, etc.), OR
Bilateral orchiectomy (surgical castration)
Technology requirement: candidates must have access to the internet
Able to understand and willing to sign a written informed consent document.
Able to speak and understand English, in the opinion of the treating physician.
Exclusion Criteria:
Significant concurrent medical or psychiatric condition that would interfere with the patient's ability to abide by the study protocol or cooperate fully with the protocol requirements, including completion of survey and assessment
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There are 6 Locations for this study
Tampa Florida, 33612, United States
Atlanta Georgia, 30322, United States
Baltimore Maryland, 21231, United States
New York New York, 10065, United States
Chapel Hill North Carolina, 27599, United States
Durham North Carolina, 27710, United States
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