Not yet recruiting NCT07518888
Exercise-induced Steroid Changes in Active Surveillance for Prostate Cancer
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: High-Intensity Interval Training (HIIT) Exercise.
- Who it may be relevant to
- Registry conditions: Prostate Cancer. Basic parameters: 18 years — 80 years · Male.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
The purpose of this research study is to understand how a short session of a home-based bodyweight high-intensity interval training (HIIT) affects steroid hormone levels in men on active surveillance for low-grade prostate cancer.
Interventions
- Behavioral High-Intensity Interval Training (HIIT) Exercise
Participants will complete a single supervised, online high intensity interval training (HIIT) exercise session lasting approximately 20 minutes. The exercise protocol consists of six 1-minute bouts with 1-minute rest intervals of moderate to high intensity bodyweight exercises, including movements such as lateral squats, wall pushups, and chair assisted sit to stands.
Primary outcome measures
- Protocol Completion Rate [Time frame: From enrollment through completion of all study procedures (up to Day 1)]
Secondary outcome measures (1)
- Acceptability of the Exercise and Saliva Collection Protocol [Time frame: Immediately after protocol completion (Day 1)]
Eligibility criteria
Inclusion criteria
- Males 18 to 80 years old
- Diagnosis of localized prostate cancer
- Currently under active surveillance
- Ability to perform moderate-to-high intensity physical activity as demonstrated by self-assessment using the Physical Activity Readiness Questionnaire (PAR-Q+)
- Able to independently perform activities of daily living, without limitations in mobility
- Ability to read, write, speak, and understand English
- Able and willing to sign consent and comply with study requirements
Exclusion criteria
- Males currently receiving treatment for prostate cancer
- Diagnosis of metastatic prostate cancer
- Individuals with medical conditions contraindicating exercise
- Uncontrolled cardiovascular or circulatory diseases, hypertension, and diabetes, as determined by the study doctor or treating physician
- Ongoing use of medications affecting steroid metabolism
- Unable to sign consent and/or comply with study requirements
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Basic science
Study locations
United States · 1 center
- University of Miami Hospitals and Clinics — Miami
Identifiers
NCT: NCT07518888 · 20251282