--- title: "GET FIT Prostate: A Randomized Controlled Exercise Trial" nct_id: NCT03741335 overall_status: COMPLETED phase: NA sponsor: OHSU Knight Cancer Institute study_type: INTERVENTIONAL primary_condition: Prostate Carcinoma countries: United States canonical_url: "https://parkinsonspathways.com/agent/trials/NCT03741335.md" clinicaltrials_gov: "https://clinicaltrials.gov/study/NCT03741335" ct_last_update_post_date: 2025-07-02 last_seen_at: "2026-05-12T06:47:32.284Z" source: ClinicalTrials.gov (mirrored, no enrichment) --- # GET FIT Prostate: A Randomized Controlled Exercise Trial **Official Title:** Group Exercise Training for Fall Prevention and Functional Improvements During and After Treatment for Prostate Cancer **NCT ID:** [NCT03741335](https://clinicaltrials.gov/study/NCT03741335) ## Key Facts - **Status:** COMPLETED - **Phase:** NA - **Study Type:** INTERVENTIONAL - **Target Enrollment:** 284 - **Lead Sponsor:** OHSU Knight Cancer Institute - **Collaborators:** National Cancer Institute (NCI), Oregon Health and Science University - **Conditions:** Prostate Carcinoma - **Start Date:** 2019-02-05 - **Completion Date:** 2024-06-30 - **CT.gov Last Update:** 2025-07-02 ## Brief Summary The GET FIT Prostate trial (Group Exercise Training for Fall prevention and functional Improvements during and after Treatment for Prostate cancer) is a single-blind, parallel group, randomized controlled trial comparing - 1) tai ji quan (functional balance) and 2) strength training (functional strength) against each other and vs. 3) a stretching control (functional mobility) - over a 6-mos. supervised intervention and 6-mos. follow-up. Two million prostate cancer survivors are alive in the U.S. and nearly half (45%) will receive androgen deprivation therapy (ADT) to reduce tumor androgen exposure and slow down cancer progression. While beneficial for cancer survival, significant treatment-induced side effects from ADT may lead to serious health consequences including falls, frailty, and dysfunction that contribute to morbidity and mortality ## Detailed Description PRIMARY OBJECTIVE: I. To determine and compare the efficacy of tai ji quan training and strength training in reducing the incidence of falls in prostate cancer survivors on antiandrogen therapy (ADT). SECONDARY OBJECTIVE: I. To determine and compare the efficacy of tai ji quan training and strength training to reduce frailty and dysfunction in prostate cancer survivors on ADT. TERTIARY OBJECTIVE: I. To determine how well the benefits of tai ji quan and strength interventions persist over a 6-month period. EXPLORATORY OBJECTIVE: I. To explore the patterns and predictors of types of men (including host and treatment factors) who benefit most from tai ji quan and strength training. OUTLINE: The study is a 3-group, single-blind, parallel design randomized controlled trial in prostate cancer survivors treated with ADT. Participants in each study group will attend supervised 1-hr classes, 3 days a week for 6 months. ARM 1: Tai ji quan, an integrated exercise routine consisting of 8 purposeful movement forms and a set of therapeutic movements, specifically designed to challenge limits of stability and train gait patterns, as reflected in movements such as upright trunk positioning, displacement of body's center of mass over the weight-bearing leg, and step initiation, locomotion, and termination. ARM 2: Strength training. Participants wear a weighted vest while performing exercises using functional movement patterns that challenge balance by using muscle groups and movement involved in everyday activities (chair rises, 90°squats, side-to-side squats, toe raises, lunges (forward, lateral, backward, walking), multi-directional step ups). ARM 3: Stretching control. Participants in the control group will attend a supervised flexibility program of the same total weekly duration as the experimental arms (e.g., 3, 60-min sessions per week). Control participants will perform a series of whole body stretching exercises, according to the ACSM guidelines for flexibility training, with a focus on developing and maintaining a healthy back. Six Month Follow-Up: Participants will be followed for an additional 6 months after the 6-month supervised intervention stops to track falls (using same monthly report used during intervention phase). Exercise questionnaires to track participation in home or community exercise programs and will be collected at the 9- and 12-month time periods. ## Eligibility - **Minimum age:** 18 Years - **Maximum age:** 100 Years - **Sex:** MALE - **Healthy Volunteers:** No ``` Inclusion Criteria: * Diagnosed with histologically confirmed prostate cancer (confirmed by self-report on Health History Questionnaire. In the case a participant isn't able to confirm this criterion, a letter will be sent to his physician.) * Currently on ADT for \>= 6 months OR not currently receiving ADT, but received \>= 6-month course within the last 10 years (confirmed by self-report on Health History Questionnaire. In the case a participant isn't able to confirm this criterion, a letter will be sent to his physician.) * If they have had other treatment, such as surgery, radiation or chemotherapy, it must have been completed \>= 6 weeks prior to enrollment and no concurrent adjuvant therapy other than ADT for prostate cancer (confirmed by self-report on Health History Questionnaire. In the case a participant isn't able to confirm this criterion, a letter will be sent to his physician). * Meets criteria for having experienced \>= 1 fall in the last year (confirmed by self-report on Health History Questionnaire) or if no falls, meets criteria for slow Timed Up and Go (TUG) time (\>= 12.0 seconds) OR slow chair stand time (\>= 10.0 seconds) (confirmed by baseline screening testing). Exclusion Criteria: * Current participation in moderate or vigorous lower-body strength training two or more times per week for 30 minutes or more or participating in tai chi two or more times per week for 30 minutes or more (confirmed by self-report on Health History Questionnaire or by discretion of the principal investigator). * Cognitive difficulties that preclude answering the survey questions, participating in the exercise classes or performance tests, or providing informed consent (Confirmed by the professional opinion of the principal investigator, Dr. Kerri Winters-Stone.). * A medical condition, movement or neurological disorder, or medication use that contraindicates participation in moderate intensity exercise (Confirmed by self-report on the Health History Questionnaire, and/or by physician clearance. If in the professional opinion of the principal investigator, Dr. Kerri Winters-Stone, contraindications other than those identified by the patient or physician are present, she may consider the participant ineligible.). * Not medically cleared for participation in moderate intensity exercise. (Confirmed by physician clearance.). * Knowingly unable to attend \> 75% of the intervention classes due to conflict with the designated time of day, days of the week, and/or location for the exercise class which they initially enrolled. (Confirmed by documentation in the Case Report Form titled "CRF - Participant Contact Info\_GET FIT Prostate"). * Not fluent in English and therefore incapable of answering survey questions, participating in class, following directions during performance testing, and providing informed consent when English is the language used. (Confirmed by documentation in the Case Report Form titled "CRF - Participant Contact Info\_GET FIT Prostate" or the professional opinion of the principal investigator, Dr. Kerri Winters-Stone.). ``` ## Arms - **Strength Training** (EXPERIMENTAL) — Participants wear a weighted vest while performing exercises using functional movement patterns used in everyday activities (chair rises, 90° squats, side-to-side squats, toe raises, lunges (forward, lateral, backward, walking), multi-directional step ups). Participants attend supervised, group-based moderate-intensity strength training program remotely 3 times per week for 60 minutes per session. - **Stretching Control** (ACTIVE_COMPARATOR) — Participants attend a supervised flexibility program where they will perform a series of whole body stretching exercises with a focus on developing and maintaining a healthy back. Participants attend a supervised, group-based supervised flexibility program remotely 3 times per week for 60 minutes per session. - **Tai Ji Quan Training** (EXPERIMENTAL) — An integrated exercise routine consisting of 8 purposeful movement forms and a set of therapeutic movements. Participants attend a supervised, group-based tai ji quan program remotely where they perform an integrated exercise routine consisting of 8 purposeful movement forms and a set of therapeutic movements 3 times per week for 60 minutes per session. ## Interventions - **Resistance Training** (OTHER) — Participants attend supervised, group-based moderate-intensity strength training program 3 times per week for 60 minutes per session. - **Stretching** (OTHER) — Participants attend a supervised, group-based supervised flexibility program 3 times per week for 60 minutes per session - **Tai Chi** (OTHER) — Participants attend a supervised, group-based tai ji quan program where they perform an integrated exercise routine consisting of 8 purposeful movement forms and a set of therapeutic movements 3 times per week for 60 minutes per session. ## Primary Outcomes - **Number of Falls** _(time frame: Baseline up to 6 months)_ — Prospective assessment of falls will be done by collecting monthly reports returned by postal and/or electronic mail. A fall is defined as unintentionally coming to rest on the ground or at some other lower level, not as a result of a major intrinsic event (e.g., stroke or syncope) or overwhelming hazard. ## Secondary Outcomes - **Change in Total Frailty Score** _(time frame: Baseline up to 12 months)_ - **Lean Body Mass** _(time frame: Baseline up to 12 months)_ - **Fatigue-general** _(time frame: Baseline up to 12 months)_ - **Fatigue-cancer** _(time frame: Baseline up to 12 months)_ - **Physical Activity** _(time frame: Baseline up to 12 months)_ - **Walk Speed** _(time frame: Baseline up to 12 months)_ - **Muscle Strength** _(time frame: Baseline up to 12 months)_ - **Change in Functional Mobility** _(time frame: Baseline up to 12 months)_ - **Change in Functional Balance** _(time frame: Baseline up to 12 months)_ - **Change in Perceived Physical Function** _(time frame: Baseline up to 12 months)_ - **Flexibility** _(time frame: Baseline up to 12 months)_ ## Locations (1) - OHSU Knight Cancer Institute, Portland, Oregon, United States ## Recent Field Changes (last 30 days) - `status.overallStatus` — added _(2026-05-12)_ - `status.primaryCompletionDate` — added _(2026-05-12)_ - `status.completionDate` — added _(2026-05-12)_ - `status.lastUpdatePostDate` — added _(2026-05-12)_ - `design.phases` — added _(2026-05-12)_ - `design.enrollmentCount` — added _(2026-05-12)_ - `eligibility.criteria` — added _(2026-05-12)_ - `eligibility.minAge` — added _(2026-05-12)_ - `eligibility.maxAge` — added _(2026-05-12)_ - `eligibility.sex` — added _(2026-05-12)_ - `outcomes.primary` — added _(2026-05-12)_ - `outcomes.secondary` — added _(2026-05-12)_ - `armsInterventions.arms` — added _(2026-05-12)_ - `armsInterventions.interventions` — added _(2026-05-12)_ - `sponsor.lead` — added _(2026-05-12)_ - `sponsor.collaborators` — added _(2026-05-12)_ - `results.hasResults` — added _(2026-05-12)_ - `locations.ohsu knight cancer institute|portland|oregon|united states` — added _(2026-05-12)_ --- *Canonical: https://parkinsonspathways.com/agent/trials/NCT03741335.md* *Source data (authoritative): https://clinicaltrials.gov/study/NCT03741335* *This page is a raw mirror with no AI summary, no editorial enrichment, and no Parkinson's-specific filtering.*