Supportive Therapy in Androgen Deprivation Clinic in Improving Health Outcomes and Managing Side Effects in Patients With Prostate Cancer

Stopped early · Phase 2

Conditions studied: Prostate Adenocarcinoma

In brief

This pilot partially-randomized phase II trial studies how well Supportive Therapy in Androgen Deprivation (STAND) clinic works in improving health outcomes and managing side effects in patients with prostate cancer. Individualized counseling regarding exercise and dietary habits may help improve patient understanding, satisfaction, and overall lessen adverse impact on quality of life caused by androgen deprivation.

Key facts

Study ID

NCT02168062

Run by

University of California, San Francisco

People needed

57

Starts

2014-06-16

Expected to finish

2018-05-22

Last updated by the study team

2020-07-23

Who can join

Age: any. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Histologic confirmation of adenocarcinoma of the prostate
• Receiving or planning to receive androgen deprivation therapy (ADT) with luteinizing hormone-releasing hormone (LHRH) agonist or antagonist
• Expected duration of ADT at least 12 months from date of study consent
• Concurrent antiandrogen therapy allowed but not required
• First dose of LHRH agonist or antagonist no more than 6 months prior to date of study content
• Prior/concurrent radiation allowed
• Other investigational agents in addition to LHRH agonist/antagonist are allowed (e.g. novel anti-androgens, androgen synthesis inhibitors)
• Prior androgen deprivation therapy allowed, provided there is documented evidence of testosterone recovery to > 150 ng/dL and greater than 12 months duration between last ?effective? date of ADT and date of study consent
• Randomized cohort only:
• No prior chemotherapy within 12 months of start date of study
• No planned chemotherapy at least 12 months from study entry
• Non-randomized pilot cohort:
• Concurrent chemotherapy (initiated within 3 months of study entry) or planned chemotherapy within 3 months of study entry
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 ? 2
• Ability to sign written informed consent
• Willing to attend monthly clinic visits at University of California, San Francisco (UCSF)

You may not qualify if…

• Physically unable or unwilling to participate in recommended exercise programs or travel to UCSF on a monthly basis
• Presence of permanent pacemaker or implantable medical device
• Artificial joint prostheses and venous filters are allowed

Where it is running

• University of California, San Francisco — San Francisco, California, United States

Full record on ClinicalTrials.gov

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