RE-FIT: Remote Exercise for WTC Responders with Prostate Cancer

This study, called RE-FIT, is looking at a Remote Supervised Exercise Program for men who responded to the World Trade Center (WTC) disaster and have prostate cancer. Many WTC responders with prostate cancer experience ongoing physical challenges. This program aims to help improve strength, balance, and overall well-being. You might be able to join if you are a WTC Health Program-certified male with prostate cancer, are 55 or older, have completed initial cancer treatment, and have low levels of regular physical activity. The researchers will be looking at how many people join the study, how many stay in the study, and how well participants stick to the exercise program. The current status of this study is unclear.

Study design
This study is an interventional study planning to enroll 40 male participants. It is testing a Remote Supervised Exercise Program.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The study measures recruitment and retention rates from the start through completion of enrollment (up to 24 months), and intervention adherence during weeks 1-16 of the intervention period.

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NCT07440641

RE-FIT (Remote Exercise for Physical Function in WTC Responders With Prostate Cancer)

Not Yet Recruiting
NAAges 55+InterventionalSupportive care
University of Vermont
~40 participants
Updated 2026-02-27 on ClinicalTrials.gov
What's tested:Remote Supervised Exercise Program

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Recruitment Rate
Measured over Recruitment assessed from study start through completion of enrollment (up to 24 months)
+3 more outcomes measured
Prostate Cancer
1 sites across 1 states
Vermont1

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Eligibility criteria

Inclusion

World Trade Center (WTC) Health Program-certified diagnosis of prostate cancer
Completed initial treatment for prostate cancer (for example, surgery or radiation); participants may be on active surveillance or receiving androgen deprivation therapy
Low levels of regular physical activity (less than 90 minutes per week of moderate-to-vigorous activity and/or less than two strength-training sessions per week)
Able to understand and provide written informed consent (electronically or by mail)
Willing and able to participate in remotely delivered exercise sessions using videoconferencing

Exclusion

Metastatic cancer
Unable to ambulate independently, with or without an assistive device
Moderate or severe cognitive impairment
Unable to communicate in English
Unable or unwilling to attend scheduled exercise sessions (three times per week for 16 weeks)
Current participation in another structured exercise program or clinical trial that could confound study outcomes
Unstable or serious medical conditions that would pose a safety risk or limit compliance (for example, uncontrolled cardiovascular disease, severe psychiatric illness, or organ failure)
  • Recruitment RateRecruitment assessed from study start through completion of enrollment (up to 24 months)

    Proportion of eligible participants who enroll in the study among those approached for participation. Unit of Measure: Percentage (%)

  • Retention RateFrom study start through completion of enrollment (up to 24 months)

    Proportion of enrolled participants who complete the 16-week post-intervention assessment. Unit of Measure: Percentage (%)

  • Intervention AdherenceWeeks 1-16 of the intervention period

    Mean percentage of planned exercise sessions attended among participants randomized to the intervention arm (48 planned sessions over 16 weeks). Unit of Measure: Percentage (%)

  • Assessment Completion RateBaseline through 16-week post-intervention assessment

    Proportion of participants completing baseline and post-intervention assessments (physical function testing and questionnaires). Unit of Measure: Percentage (%).