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NCT Number: NCT06165302

Exercise in Prostate Cancer

The goal of this clinical trial is to learn how exercise intervention affects circulating tumor cells (CTC) in men with advanced prostate cancer. The primary objective is to determine if an exercise intervention decreases CTCs in men with advanced prostate cancer. Participants will have baseline screening assessments, followed by 12 weeks of exercise intervention, and then follow-up assessments 12 weeks after the end of the exercise intervention.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Johns Hopkins University

Baltimore, Maryland, 21287, United States

Location status: Recruiting

Location contact

Niya Research Coordinator

CONTACT

[email protected]

410-955-1017

About this study

This is a pilot single arm prospective study of personalized exercise training in men with metastatic castration resistant prostate cancer who are being treated with or without oral anti-androgens. The primary objective is to determine if combination of resistance and aerobic exercises lowers CTCs in men with mCRPC. Researchers will assess the rate of conversion from CTC positive to CTC negative in participants at the end of the 12 week exercise intervention. The study will enroll 20 participants onto the trial with the goal of at least 10 participants having blood drawn at both baseline and 12 weeks and completed at least 75% of the prescribed exercise sessions. Participants will undergo follow-up assessments at the end of the 12 week exercise intervention and the study team will monitor participant records for 365 days after the study completion for vital status.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men with metastatic prostate adenocarcinoma
  • Currently taking androgen deprivation therapy alone or with an oral androgen axis inhibitor (abiraterone, enzalutamide, darolutamide, or apalutamide are permitted) and have been on treatment for at least 3 months
  • Elevated (PSA > 1ng/mL) or rising PSA (any numerical increase based on at least 2 PSA readings at least 2 weeks apart)
  • Any number of prior therapies (prior chemo, radium-223, etc.) is allowed
  • CTC + according to standard clinical grade laboratory test by androgen receptor isoform splice variant 7 (AR-V7) testing at Hopkins.
  • If a bone protective agent is to be started, it should be started at least 2 weeks prior to the onset of exercise intervention.
  • Eastern Cooperative Oncology Group (ECOG) performance status <=1
  • Clearance by cardiologist if under the current care of a cardiologist (seen in the past 1 year)
  • Age <=80 years

Exclusion criteria

  • Small cell carcinoma of the prostate
  • Unable to participate or monitor exercise compliance due to conditions such as impaired cognition
  • Moderate to severe bone pain that limits any activities of daily living, including use of narcotics for prostate cancer related pain
  • Clinical progression requiring a change in systemic therapy or the addition of palliative radiation for symptom control
  • Bone metastases in spine or long bones which, in the eye of the treating physician require referral to radiation oncology or surgery for management due to risk of fracture
  • Significant cardiovascular disease or concurrent illness that would make exercise intervention for 12 weeks unsafe. If there is significant cardiovascular disease and the participant is under the care of a cardiologist (seen within the past 1 year), approval of the cardiologist to participate is required.
  • Major surgery within the past 4 weeks

Treatment and study plan

Exercise Intervention

Behavioral

12 weeks of prescribed exercise intervention.

Primary outcomes

  1. Number of participants with negative CTC count

    Time frame: Baseline, 12 weeks

    Number of participants with negative CTC count at 12 weeks compared to the baseline

Secondary outcomes

  1. Number of participants with change in cell free DNA levels

    Time frame: Baseline, 12 weeks

    Number of participants with change in cell free DNA levels from baseline to 12 weeks

  2. Number of participants with change in Cell free RNA levels

    Time frame: Baseline, 12 weeks

    Number of participants with change in cell free RNA levels from baseline to 12 weeks

Study contacts

Contact information is provided by the study sponsor or research team.

Rana Sullivan, RN

CONTACT

[email protected]

410-614-6337

Sponsors and collaborators

Lead sponsor

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Other

Collaborators

  • Physical Medicine & Rehabilitation Educ Research Foundation, Inc

Registry information

Official study title

EPC Trial: Exercise in Prostate Cancer

Important dates

Study start
2025
Primary completion
2029
Study completion
2030
First posted
Dec 11, 2023
Registry last updated
Oct 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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