NRG-CC007CD

Terminated

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Protocol Information

Tab containing protocol details, study design, and eligibility criteria
Tab containing study documents, informed consent forms, and study materials
Tab containing information for potential study participants

Increasing the Dose of Survivorship Care Planning in Prostate Cancer Survivors Who Receive Androgen Deprivation Therapy

Principal Investigator

Ronald Chen, MD MPH

Status

Terminated

Open to Accrual

March 27, 2019

Closed to Accrual

July 28, 2022

Closed to Accrual & Treatment

January 7, 2025

Terminated

September 4, 2025


Disease Site

Cancer Care Delivery Research [CD] Other

Phase

Other

Developmental Therapeutics

No

Primary Objective

To determine if the experimental arm (increased doses of SCP) has more patients who saw a primary care provider and had blood glucose and cholesterol checked in Year 2 (13-24 months) after finishing RT as compared to the control arm.

Patient Population

The participant must have a diagnosis of prostate adenocarcinoma that will be treated with RT plus ADT with curative intent.  Both definitive RT (intact prostate) and post-prostatectomy RT patients are eligible.  

Target Accrual

504

Protocol Documents

Available via the National Cancer Institute (NCI) Cancer Trials Support Unit (CTSU) website.


Patient Study Webpage

There is no available patient study webpage available for this trial at this time.