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Purpose

The purpose of this study is to determine whether a 16-week supervised, clinic-based circuit training intervention utilizing resistance and functional exercises and self-directed aerobic exercise will improve frailty and sarcopenic status and disease progression outcomes among pre-frail/frail metastatic prostate cancer patients receiving androgen deprivation therapy (ADT). The names of the study intervention involved in this study is: • Supervised circuit training (aerobic and resistance exercise regimen)

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Ability to understand and the willingness to sign informed consent prior to any study-related procedures. - Diagnosed with metastatic prostate cancer. - Aged ≥18 years; due to the rarity of the disease in those <18 years, this age bracket will not be included. - Have been receiving androgen deprivation (either with or without androgen receptor targeted treatment) for at least one month and expect to remain on their treatment for at least 4 months. - Are pre-frail or frail as indicated by the FRAIL scale (a score of 1-2 = pre-frail; 3-5 = frail). - Have physician's clearance to participate in exercise. - Speak English. - Participate in less than 2 structured resistance exercise sessions per week over the last 4 months. - Participate in less than or equal to 60 minutes of moderate-to-vigorous aerobic exercise per week over the last month. - Willing to travel to Dana-Farber Cancer Institute for necessary data collection and exercise sessions.

Exclusion Criteria

  • Receiving chemotherapy. This study is exclusively targeting androgen deprivation therapy-related effects. - Have unstable bone lesions. In general patients with severely symptomatic/unstable bone lesions due to bone metastases are at a higher risk of fractures. - Complete 2 or more structured resistance exercise sessions per week over the last 4 months and participate in more than 60 minutes of moderate-to-vigorous aerobic exercise per week over the last month. Excess additional exercise is a confounding factor in assessing the effect of the current exercise program. - Unstable comorbidities that prevent participation in moderate-to-vigorous intensity exercise. Patients with unstable comorbidities likely require supervised exercise for safety, and part of this study involves unsupervised exercise; therefore, for safety reasons, these persons are excluded. - Patients receiving treatment for other active malignancies (except basal cell carcinoma). This study is exclusively targeting androgen deprivation therapy-related effects. - Subjects who in the opinion of the investigators may not be able to comply with the safety monitoring requirements of the study.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Supportive Care
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Exercise Group 		Participants will partake in a 16-week supervised exercise program.
  • Behavioral: Supervised Circuit Training
    16-week, multicomponent exercise intervention comprised of sessions supervised by certified exercise oncology trainer and home-based, self-directed aerobic exercises. Stationary bike and accelerometer (activity/heart rate monitor) will be provided.
Experimental
Attention Control Group 		Participants will continue with their normal daily activities.
  • Behavioral: Supervised Circuit Training
    16-week, multicomponent exercise intervention comprised of sessions supervised by certified exercise oncology trainer and home-based, self-directed aerobic exercises. Stationary bike and accelerometer (activity/heart rate monitor) will be provided.

Recruiting Locations

Brigham and Women's Hospital
Boston, Massachusetts 02215
Contact:
Christina Dieli-Conwright, PhD, MPH
617-582-8321
ChristinaM_Dieli-Conwright@DFCI.HARVARD.EDU

More Details

Status
Recruiting
Sponsor
Dana-Farber Cancer Institute

Study Contact

Christina Dieli-Conwright, MD
617-582-8321
ChristinaM_Dieli-Conwright@dfci.harvard.edu

Detailed Description

This research study is a pilot, randomized control study, which is the first-time investigators are examining this intervention in this setting. Participants will be randomized into one of two study groups: Exercise Group versus Attention Control Group. Randomization means a participant is placed into a group by chance. The research study procedures include screening for eligibility, study treatment, including extensive evaluations of fitness, physical health and strength, blood tests, muscle biopsy, surveys, and follow-up visits. Participation in this research study is expected to last about 16 weeks. It is expected that about 80 people will take part in this research study. The Prostate Cancer Foundation is providing funding for this research study.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.