Clinical trial · Interventional
Home-based Exercise Intervention for Patients With Metastatic Prostate Cancer
Feasibility Study of a Home-Based Exercise Intervention Program for Patients With Metastatic Castration-Resistant Prostate Cancer Receiving Androgen Deprivation Therapy (ADT)
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This single arm, multi-site pilot study aims to evaluate the feasibility of recruiting and adherence to a 12 week home-based exercise intervention to be conducted in men with metastatic castration resistant prostate cancer (mCRPC) receiving androgen deprivation therapy (ADT). Thirty patients will be enrolled, with the expectation that 20-25 will complete all follow-up measures.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Androgen Deprivation Therapy | — | UNRESOLVED | — |
| Castration-resistant Prostate Cancer | Castration-Resistant Prostate Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Home-based exercise | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Home-based Exercise
- description
- The sole intervention group will complete a combination of aerobic and strength training \~3 times per week for 12 weeks with each session lasting 1 hour.
- interventionNames
- Behavioral: Home-based exercise
Primary outcomes (1)
- measure
- Percentage of Patients Who Complete the Pre/Post Exercise Intervention Testing.
- timeFrame
- 12 weeks after baseline testing
- description
- To estimate the feasibility of a 12 week, home-based exercise intervention in metastatic castrate resistant prostate cancer (mCPRC) patients undergoing androgen deprivation therapy by reporting the percentage of patients who complete the pre/post testing following the intervention. This was calculated as the number of subjects who completed the trial compared to the total number who completed baseline testing.
Secondary outcomes (19)
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Metastatic disease that has progressed despite castrate levels of testosterone (surgically or medically castrated, with testosterone levels of \< 50 ng/dL) receiving ADT. This will be verified by assessing total testosterone levels within 4 weeks prior to enrollment. * No current chemotherapy. * Patients may be receiving additional hormonal therapy agents including but not limited to antiandrogens (e.g. bicalutamide, enzalutamide) and CYP17 inhibitors (e.g. abiraterone). * Ability to engage safely in moderate exercise as determined by their treating physician. * Not previously engaged in regular exercise training (\<3 or more d/wk for \> 30 min/d or \<90 mins per week total including strength training, aerobic training, or walking) in the past 6 months. * Access to a computer or a smart phone for syncing and uploading wearable activity data. * Be able to speak and read English. Exclusion Criteria: * Any condition that causes severe pain with exertion. * History of bone fractures. * Active cardiovascular disease including any of the following: * New York Heart Association (NYHA) Grade II or greater congestive heart failure . * History of myocardial infarction or unstable angina within 6 months prior to Day 1. * History of stroke or transient ischemic attack within 6 months prior to Day 1. * Acute or chronic respiratory disease that is severe enough to compromise the ability of the participant to safely engage in exercise training protocol. * Acute or chronic bone/joint/muscular abnormalities compromising their ability to exercise. * Neurological conditions that affect balance and, or muscle strength. * Dementia, altered mental status or any psychiatric condition prohibiting the understanding or rendering of informed consent.
References
Publications (0)
Data not yet available