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RESIST-ADT (Androgen Deprivation Therapy)

Primary Purpose

Prostate Cancer, Physical Function

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Progressive Resistance Training Exercise
Flexibility and Balance Exercise
Sponsored by
Dana-Farber Cancer Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Prostate Cancer focused on measuring Prostate Cancer, Androgen Deprivation Therapy (ADT), Physical Function, Structured Exercise, Muscle Strength and Power

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Men with active Prostate Cancer who are 60 years or older.
  • Hormone-naive men about to undergo medical or surgical ADT.
  • Planned ADT for at least 6 months.
  • Life expectancy of at least 6 months from enrollment.
  • Ability and willingness to provide informed consent.

Exclusion Criteria:

  • Active medical conditions affecting participation in exercise training (limiting arthropathies, myopathies, severe peripheral vascular disease, or severe neuropathy).
  • Cardiovascular disease (current angina, severe valvular disease, advanced congestive heart failure, arrhythmias, or stroke with residual muscular weakness).
  • Prior hip or knee replacement.
  • History of lower extremity fracture in the past 6 months.

Sites / Locations

  • Dana-Farber Cancer InstituteRecruiting
  • Brigham and Women's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Progressive Resistance Training Exercise

Flexibility and Balance Exercise

Arm Description

Men with prostate cancer who are about to begin androgen-deprivation therapy (ADT) will attend structured progressive resistance exercise training sessions 2 times/week for six months.

Men with prostate cancer who are about to begin androgen-deprivation therapy (ADT) will attend flexibility and balance exercises training sessions 2 times/week for six months.

Outcomes

Primary Outcome Measures

Loaded stair climb power
Compare the efficacy of a structured resistance exercise regimen vs a structured control regimen on loaded stair climb power. Assessment of physical function as measured by Loaded Stair Climbing Power.

Secondary Outcome Measures

Body composition
Lean body mass measured by dual energy x-ray absorptiometry (DEXA)
Muscle strength and power
Maximal voluntary muscle strength in the lower extremities will be assessed by conducting the leg and chest press exercise by the 1-repetition maximum method and assessing loaded stair climb power.
Quality of Life (QOL)
Measured by SF-36 questionnaire a multi-purpose survey designed to capture adult patients' perceptions of their own health and well-being
Fatigue
Fatigue will be assessed by the Functional Assessment of Chronic Illness Therapy fatigue scale (FACIT-F).

Full Information

First Posted
July 22, 2020
Last Updated
August 14, 2023
Sponsor
Dana-Farber Cancer Institute
Collaborators
National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT04485767
Brief Title
RESIST-ADT (Androgen Deprivation Therapy)
Official Title
Preventing a Decline in Physical Function in Older Androgen-Deprived Men With Structured Exercise Training (RESIST-ADT Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2020 (Actual)
Primary Completion Date
July 31, 2024 (Anticipated)
Study Completion Date
October 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dana-Farber Cancer Institute
Collaborators
National Institute on Aging (NIA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The overall goal of this study is to determine if implementing structured exercises prevent decline in muscle mass, muscle strength and physical function in men with prostate cancer undergoing androgen deprivation therapy (ADT). Our main hypothesis is that structured resistance exercise training in men undergoing ADT will preserve physical function assessed by loaded stair climbing power compared with the control group. The trial will also examine the efficacy of the exercise regimen on muscle strength, QOL and fatigue. The findings of this trial will lay the groundwork for definitive intervention trials to prevent frailty and falls in these men.
Detailed Description
This randomized, controlled, parallel group trial of 6-months duration is determining the efficacy of structured resistance exercise training in preventing the decline in physical function in older men with prostate cancer undergoing androgen deprivation therapy (ADT). It will compare the structured resistance exercise training with a control group of men undergoing flexibility and balance exercises training. Men undergoing ADT for treatment of their prostate cancer experience a significant decline in muscle mass and muscle strength, which impacts their physical function. This predisposes them to frailty and a higher risk of falls. In addition to physical dysfunction, men undergoing ADT also experience a significant decrease in health-related quality of life and experience fatigue (tiredness). This research study is taking a preventative approach to the physical function problems in men with prostate cancer by implementing exercise interventions before participants begin ADT that are specifically designed to improve muscle mass, muscle strength and physical function to lessen the impacts of muscle mass and strength decline. The study includes a screening visit during which the following procedures will be conducted: Vitals, EKG, blood sample collection and a physical to determine eligibility. If qualified, participants will be randomly assigned to two different types of structured exercises: Resistance exercise training or flexibility and balance exercises. During the weekly exercise training 20 subjects will be assigned to the Exercise A group and 20 subjects to the Exercise B group. The exercise training sessions will occur approximately 2 times/week. In addition participants will also undergo DEXA scans, perform muscle strength testing and complete questionnaires at baseline, 3- and 6-month visits. It is expected participants will be in this research study for up to 6 months. It is expected that about 40 people will take part in this research study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer, Physical Function
Keywords
Prostate Cancer, Androgen Deprivation Therapy (ADT), Physical Function, Structured Exercise, Muscle Strength and Power

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Structured Resistance Exercise vs Control Exercise
Masking
ParticipantInvestigator
Masking Description
Participants, Investigators and Research Staff will remain blinded. Only exercise personnel and study statistician will be unblinded.
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Progressive Resistance Training Exercise
Arm Type
Experimental
Arm Description
Men with prostate cancer who are about to begin androgen-deprivation therapy (ADT) will attend structured progressive resistance exercise training sessions 2 times/week for six months.
Arm Title
Flexibility and Balance Exercise
Arm Type
Active Comparator
Arm Description
Men with prostate cancer who are about to begin androgen-deprivation therapy (ADT) will attend flexibility and balance exercises training sessions 2 times/week for six months.
Intervention Type
Behavioral
Intervention Name(s)
Progressive Resistance Training Exercise
Intervention Description
Progressive Resistance Training Exercise 2x weekly for 6 months.
Intervention Type
Behavioral
Intervention Name(s)
Flexibility and Balance Exercise
Intervention Description
Flexibility and Balance Exercise Training Exercise 2x weekly for 6 months.
Primary Outcome Measure Information:
Title
Loaded stair climb power
Description
Compare the efficacy of a structured resistance exercise regimen vs a structured control regimen on loaded stair climb power. Assessment of physical function as measured by Loaded Stair Climbing Power.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Body composition
Description
Lean body mass measured by dual energy x-ray absorptiometry (DEXA)
Time Frame
6 months
Title
Muscle strength and power
Description
Maximal voluntary muscle strength in the lower extremities will be assessed by conducting the leg and chest press exercise by the 1-repetition maximum method and assessing loaded stair climb power.
Time Frame
6 months
Title
Quality of Life (QOL)
Description
Measured by SF-36 questionnaire a multi-purpose survey designed to capture adult patients' perceptions of their own health and well-being
Time Frame
6 months
Title
Fatigue
Description
Fatigue will be assessed by the Functional Assessment of Chronic Illness Therapy fatigue scale (FACIT-F).
Time Frame
6 months

10. Eligibility

Sex
Male
Gender Based
Yes
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men with active Prostate Cancer who are 60 years or older. Hormone-naive men about to undergo medical or surgical ADT. Planned ADT for at least 6 months. Life expectancy of at least 6 months from enrollment. Ability and willingness to provide informed consent. Exclusion Criteria: Active medical conditions affecting participation in exercise training (limiting arthropathies, myopathies, severe peripheral vascular disease, or severe neuropathy). Cardiovascular disease (current angina, severe valvular disease, advanced congestive heart failure, arrhythmias, or stroke with residual muscular weakness). Prior hip or knee replacement. History of lower extremity fracture in the past 6 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shehzad Basaria, MD
Phone
617-525-9144
Email
sbasaria@bwh.harvard.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Milena Braga, MD
Phone
617-525-9144
Email
mbraga2@bwh.harvard.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shehzad Basaria, MD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thomas Storer, PhD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dana-Farber Cancer Institute
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02066
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shehzad Basaria, MD
Phone
617-525-9144
Email
sbasaria@bwh.harvard.edu
First Name & Middle Initial & Last Name & Degree
Milena Braga, MD
Phone
617-525-9144
Email
mbraga2@bwh.harvard.edu
First Name & Middle Initial & Last Name & Degree
Shehzad Basaria, MD
First Name & Middle Initial & Last Name & Degree
Thomas Storer, PhD
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shehzad Basaria, MD
Phone
617-525-9144
Email
sbasaria@bwh.harvard.edu
First Name & Middle Initial & Last Name & Degree
Milena Braga, MD
Phone
617-525-9144
Email
mbraga2@bwh.harvard.edu
First Name & Middle Initial & Last Name & Degree
Shehzad Basaria, MD
First Name & Middle Initial & Last Name & Degree
Thomas Storer, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The Dana-Farber / Harvard Cancer Center encourages and supports the responsible and ethical sharing of data from clinical trials. De-identified participant data from the final research dataset used in the published manuscript may only be shared under the terms of a Data Use Agreement. Requests may be directed to: [contact information for Sponsor Investigator or designee]. The protocol and statistical analysis plan will be made available on Clinicaltrials.gov only as required by federal regulation or as a condition of awards and agreements supporting the research.
IPD Sharing Time Frame
Data can be shared no earlier than 1 year following the date of publication
IPD Sharing Access Criteria
BWH - Contact the Partners Innovations team at http://www.partners.org/innovation DFCI - Contact the Belfer Office for Dana-Farber Innovations (BODFI) at innovation@dfci.harvard.edu

Learn more about this trial

RESIST-ADT (Androgen Deprivation Therapy)

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