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Prostate CancerNCT05918263

Exercise for Tumor Suppressive Impact in Men With Prostate Cancer at High-Risk of Progression on Active Surveillance: The REMOVE Trial

A study testing High-Intensity Interval Training Exercise Program in people with Prostate Cancer and Prostatic Neoplasms, run by Fred Hutchinson Cancer Center at 4 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The purpose of this study is to determine whether a 12-week, home-based, virtually supervised exercise program will slow cancer progression of prostate cancer among men with prostate cancer at high-risk of progression undergoing active surveillance. Read more about this study

Who is it for?
Ages 18 years and older, men only
Conditions the study is for
Prostate Cancer, Prostatic Neoplasms
What is being tested?
High-Intensity Interval Training Exercise Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
68 participants
Where
4 sitesUnited States
Study dates
1 Jan 2024to 31 Mar 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Men only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age ≥18 years.
  • Histologically diagnosed with localized prostate cancer.
  • Initiating or undergoing active surveillance.
  • Having a higher risk of progression, defined as meeting one or more of the following: (1) favorable- intermediate risk prostate tumor at diagnosis, (2) obesity (body mass index ≥ 30), and/or (3) self- identified as Black or African American.
  • No plans for invasive treatment for their prostate cancer in the 12 weeks following the time of enrollment.
  • Ability to understand and willingness to provide informed consent.

Who cannot join

  • Received any invasive curative-intent treatment for prostate cancer, including surgery, chemotherapy, radiation therapy, and hormonal therapy.
  • Patients with metastasis and/or other active malignancies (except basal cell carcinoma) and/or receiving treatment for those malignancies.
  • Participating in any (>0 min/week) high-intensity exercise at the time of recruitment.
  • Having chronic medical conditions that are clinically unstable or uncontrolled with medications, deemed high-risk for exercise. These include but are not limited to unstable cardiac diseases, uncontrolled diabetes, and bone metastases with imminent risk of fracture.
  • Having a high risk for noncompliance with study procedures. This will be determined by the study team based on the history of missed oncology appointments (i.e., ≥3 no-shows in 6 months) and poor responsiveness during recruitment (i.e., ≥3 unreturned contacts).
  • Patients who are non-English speaking and unable to complete the participant surveys.

Trial locations and contacts

4 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Dong-Woo Kang, PhD contact

206-667-5188

dkang@fredhutch.org

United States4 sites, 1 recruiting
  • Beth Israel Deaconess Medical Center

    Boston, Massachusetts, 02215

    Completed
  • Brigham and Women's Hospital

    Boston, Massachusetts, 02215

    Completed
  • Dana-Farber Cancer Institute

    Boston, Massachusetts, 02215

    Completed
  • Fred Hutch/University of Washington Cancer Consortium

    Seattle, Washington, 98109

    Dong-Woo Kang, PhD, 206-667-5188, dkang@fredhutch.org

    Dong-Woo Kang, PhD

    Recruiting

Other trials in United States

About this study

The purpose of this study is to determine whether a 12-week, home-based, virtually supervised exercise program will slow cancer progression of prostate cancer among men with prostate cancer at high-risk of progression undergoing active surveillance.

The name of the study intervention involved in this study is:

Aerobic high-intensity interval training (HIIT) (training exercise intervention)

Read the detailed description

This research study is a randomized controlled study for a home-based, virtually supervised, aerobic exercise intervention for men with prostate cancer at high-risk of progression undergoing active surveillance. There is evidence that exercise may suppress cancer progression, but the evidence is preliminary.

Participants will be randomized into one of two treatment groups: Group A: Aerobic high-intensity interval training (HIIT) versus Group B: Waitlist Control. Randomization means a participant is placed into a study group by chance.

The research study procedures include screening for eligibility, study treatment visits, survey questionnaires, blood tests, and follow-up visits.

Participation in this research study is expected to last about 14 weeks.

It is expected that about 68 people will take part in this research study.

The Prostate Cancer Foundation is providing funding for this research study.

Being tested
High-Intensity Interval Training Exercise Program
Keywords
Prostate Cancer, Prostatic Neoplasms
Medical subject headings
Prostatic Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • High-Intensity Interval Training Exercise ProgramBehavioural

    Home-based, virtually supervised, aerobic exercise program of 36 sessions accessible via internet-enabled tablet (provided to participant if needed). Participants will be supplied with stationary bike, heart rate monitor, and blood pressure monitor.

  • High-Intensity Interval Training Exercise ProgramBehavioural

    (Optionally) Home-based, virtually supervised, aerobic exercise program of 36 sessions accessible via internet-enabled tablet (provided to participant if needed). Participants will be supplied with stationary bike, heart rate monitor, and blood pressure monitor.

Study groups in NCT05918263
Study groupRoleWhat they receive
Group A: HIIT Exercise ProgramExperimentalParticipants will be allocated in a 1:1 ratio, using a permuted blocked design with varying block size. Study procedures will be conducted as follows: * Testing visits at Week 1 and 14 for physical exams, physical fitness and function assessments, survey questionnaires, and cardiopulmonary fitness assessment. * Virtual, aerobic training sessions three times weekly with trained oncology exercise specialist.
Receives: Behavioral: High-Intensity Interval Training Exercise Program
Group B: Waitlist ControlExperimentalParticipants will be allocated in a 1:1 ratio, using a permuted blocked design with varying block size. Study procedures will be conducted as follows: * Testing visits at Week 1 and 14 for physical exams, physical fitness and function assessments, and survey questionnaires. * Upon completion of post-intervention assessments, participants will have the option to take part in the 12-week HIIT exercise program.
Receives: Behavioral: High-Intensity Interval Training Exercise Program

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Prostate-Specific Antigen (PSA) Level

    The primary outcome is the between-group difference in prostate-specific antigen (PSA) levels post-intervention. Analysis of covariance will be used to detect the difference adjusting for baseline values of the outcome and other covariates.

    Measured: Baseline (Week 1) and post-intervention (Week 14)

Secondary outcomes (13)
  1. Prostate-Specific Antigen (PSA) Velocity

    PSA velocity will be calculated following the PSA Working Group Guidelines, using the three most recent PSA values obtained from the medical chart with the first and last values being at least three months apart. The formula was based on the natural logarithm of 2 (0.693) divided by the slope obtained from fitting a linear regression of the natural log of PSA.

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  2. Prostate-Specific Antigen (PSA) Doubling Time

    PSA doubling time will be calculated following the PSA Working Group Guidelines, using the three most recent PSA values obtained from the medical chart with the first and last values being at least three months apart. PSA velocity will be used to calculate the number of years that PSA levels become doubles, where the longer the time the better the prognosis.

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  3. Proliferation of LNCaP Prostate Cancer Cell Line

    LNCaP cells are androgen-sensitive human prostate adenocarcinoma cells. LNCaP cells will be grown in vitro and their growth rate will be measured by counting the number of cells over time.

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  4. Cardiorespiratory Fitness

    Cardiorespiratory fitness will be assessed as VO2peak by a graded maximal or submaximal cycle exercise stress test. VO2peak is defined as the highest values of oxygen uptake averaged among every 30-second interval during the test. VO2peak will be reported in both relative (ml·kg-1·min-1) and absolute (L/min) terms.

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  5. Muscular Strength

    Muscular strength will be measured as 1-repetition maximum (RM) (i.e., the greatest resistance that can be moved through the full range of motion), which has been the standard for strength assessments. 1-RM values will be estimated from 10-RM using validated equations on 2 exercises (chest press and leg press).

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  6. Short Physical Performance Battery (SPPB)

    Physical function will be assessed by the Short Physical Performance Battery (SPPB), which includes the following 3 lower extremity measures completed in the following order. Timed balance (seconds): Balance will be assessed under 3 conditions (side-by-side, semi-tandem, and tandem stands). Gait speed (seconds): Gait speed will be assessed over a 4-meter flat surface distance. The participant will be asked to complete 2 attempts of this test. Time will be recorded using an electronic timing system. Chair stand (seconds): Chair stand will be performed under 2 conditions: a) subjects will perform a single chair stand; b) subjects will be asked to perform 5 repeated chair stands as quickly as possible; time to completion will be recorded.

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  7. Health-Related Quality of Life

    The European Organization for Research and Treatment of Cancer- Quality of Life Questionnaire-C30 (EORTC-QLQ C30) will assess health-related quality of life, consisting of subscales including functional scales (physical, role, cognitive, emotional, social), symptom scales (fatigue, pain, and nausea and vomiting), global health status and quality of life scale, also several single-item symptom measures. The score ranges from 0 to 100 and a higher value indicates a better quality of life.

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  8. Prostate Cancer-Specific Anxiety

    Assessed by the Memorial Anxiety Scale for Prostate Cancer (MAX-PC), an 18-item questionnaire with a 4-point Likert-type scale asking how frequently certain "comments made by men about prostate cancer" were true of the respondent. Each item is scored from 0 to 4 with anchors ranging from "Not at all" to "Often."

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  9. Fear of Cancer Progression Assessment

    The Fear of Cancer Recurrence Inventory (FCRI) is a well-established scale for in-depth assessment of FCR in research. The short form of this measure (FCRI-SF), consisting of 9 items, has been used as a tool to screen for clinical levels of fear of cancer recurrence (FCR). The FCRI-SF is often used to identify potential cases of clinically significant FCR.

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  10. Sleep Quality

    Sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI). The PSQI is a self-rated questionnaire which assesses sleep quality and disturbances over a 1-month. The PSQI contains 19 self-rated questions and 5 questions rated by the bed partner or roommate (if one is available). Only self-rated questions are included in the scoring. The self-rated items are combined to form seven "component" scores, each of which has a range of 0-3 points, and they are summed to obtain a global score ranging from 0-21 points, where a higher score indicates worse sleep quality.

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  11. Body Composition

    Body composition will be assessed using Bioelectrical Impedance Analysis (BIA). Participants will stand on the device while holding the handles with their arms at their sides, and the device will estimate percent body fat using an algorithm based on age, sex, height, and body weight. Supporting anthropometric measures will include height (stadiometer), body weight (calibrated digital scale), and waist and hip circumference (constant-tension tape measure). Body fat will be reported as a percentage (%), with body weight reported in kilograms (kg).

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  12. Prostate Cancer Symptoms

    Prostate cancer-specific symptoms will be assessed using the Expanded Prostate Cancer Index Composite-26 (EPIC-26), a 26-item questionnaire evaluating five domains: urinary incontinence, urinary irritative/obstructive, bowel, sexual, and hormonal function. Each domain is scored from 0 to 100, where a higher score indicates better function and fewer symptoms.

    Measured: Baseline (Week 1) and post-intervention (Week 14)

  13. Exercise Benefits and Barriers

    Perceptions of the benefits of and barriers to exercise will be assessed using a study-specific Exercise Benefits/Barriers questionnaire with two parts: perceived benefits/harms of the program (7 items rated -3 [very much worse] to +3 [very much better], higher = greater benefit) and perceived barriers to completing the program (14 items rated 1 [not at all] to 7 [very much], higher = greater barriers).

    Measured: Baseline (Week 1) and post-intervention (Week 14)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jun 2023
  2. Study start1 Jan 2024
  3. Primary completion31 Mar 2027 (estimated)
  4. Study completion31 Mar 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Investigator
Enrolment
68 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05918263
Sponsor's protocol ID
RG1125288
Other IDs
20857, NCI-2023-07008
Status last verified
Jul 2026
First submitted
14 Jun 2023
Last updated
15 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing High-Intensity Interval Training Exercise Program in people with Prostate Cancer and Prostatic Neoplasms, run by Fred Hutchinson Cancer Center at 4 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 15 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Dong-Woo Kang, PhD (206-667-5188, dkang@fredhutch.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Prostate-Specific Antigen (PSA) Level (time frame: Baseline (Week 1) and post-intervention (Week 14)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Jul 2026.

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