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.
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
- Type of treatment
- Pill or oral medicine, Lifestyle or therapy programme
- 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.
United States4 sites, 1 recruiting
- Completed
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
- Recruiting
Fred Hutch/University of Washington Cancer Consortium
Seattle, Washington, 98109
Dong-Woo Kang, PhD, 206-667-5188, dkang@fredhutch.org
Dong-Woo Kang, PhD
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.
- Conditions
- Prostate Cancer, Prostatic Neoplasms
- 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 group | Role | What they receive |
|---|---|---|
| Group A: HIIT Exercise Program | Experimental | Participants 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 Control | Experimental | Participants 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.
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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.
- First posted26 Jun 2023
- Study start1 Jan 2024
- Primary completion31 Mar 2027 (estimated)
- Study completion31 Mar 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Prostate CancerStudies of the same condition, open and under way.
- More trials run by Fred Hutchinson Cancer CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Fred Hutchinson Cancer Center
- Sponsor type
- University, hospital or other
- Collaborators
- Prostate Cancer Foundation
- Responsible party
- Sponsor
- Investigators
- Dong-Woo Kang, PhD, Principal investigator, Fred Hutch/University of Washington Cancer Consortium
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
Study at a glance
From the registry record, last updated by the sponsor on 15 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Exercise for Tumor Suppressive Impact in Men With Prostate Cancer at High-Risk of Progression on Active Surveillance: The REMOVE Trial
- ClinicalTrials.gov ID
- NCT05918263
- Acronym / sponsor ID
- RG1125288
- Conditions
- Prostate Cancer, Prostatic Neoplasms
- Keywords
- Prostate Cancer, Prostatic Neoplasms
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 68 participants (estimated)
- Lead sponsor
- Fred Hutchinson Cancer CenterUniversity, hospital or other
- Collaborators
- Prostate Cancer Foundation
- Study start
- 1 Jan 2024 (actual)
- Primary completion
- 31 Mar 2027 (estimated)
- Study completion
- 31 Mar 2027 (estimated)
- First posted
- 26 Jun 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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)
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.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Group A: HIIT Exercise Program | Experimental | Behavioral: High-Intensity Interval Training Exercise ProgramParticipants 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. |
| Group B: Waitlist Control | Experimental | Behavioral: High-Intensity Interval Training Exercise ProgramParticipants 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. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- 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.
Key exclusion criteria (6 listed)
- 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).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| High-Intensity Interval Training Exercise ProgramHome-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. | Behavioural | Group A: HIIT Exercise Program |
| High-Intensity Interval Training Exercise Program(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. | Behavioural | Group B: Waitlist Control |
Primary outcome
Prostate-Specific Antigen (PSA) Level
Time frame: Baseline (Week 1) and post-intervention (Week 14)
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.
13 secondary outcomes
Prostate-Specific Antigen (PSA) Velocity
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Prostate-Specific Antigen (PSA) Doubling Time
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Proliferation of LNCaP Prostate Cancer Cell Line
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Cardiorespiratory Fitness
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Muscular Strength
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Short Physical Performance Battery (SPPB)
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Health-Related Quality of Life
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Prostate Cancer-Specific Anxiety
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Fear of Cancer Progression Assessment
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Sleep Quality
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Body Composition
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Prostate Cancer Symptoms
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Exercise Benefits and Barriers
Time frame: Baseline (Week 1) and post-intervention (Week 14)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Jul 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Dong-Woo Kang, PhD principal investigator
Fred Hutch/University of Washington Cancer Consortium
4 sites in 1 country: see every site and its status.
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.