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Exercise Training Among Men With Prostate Cancer

Primary Purpose

Prostatectomy

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Exercise
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Prostatectomy

Eligibility Criteria

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

Inclusion Criteria:

  1. Legal age (>18 years old)
  2. An interval of at least 6 weeks between prior radical prostatectomy and study enrollment
  3. Karnofsky performance status of at least 70% at study entry
  4. Estimated life expectancy of ≥6 months
  5. Ability to read and understand English
  6. Attending urologist approval
  7. Signed informed consent
  8. Willingness to be randomized; and
  9. No contraindications to exercise as recommended by the American Thoracic Society

Exclusion Criteria:

  1. Acute myocardial infarction (6 weeks)
  2. Unstable angina
  3. Uncontrolled arrhythmias causing symptoms or hemodynamic compromise
  4. Syncope
  5. Acute endocarditis
  6. Acute myocarditis or pericarditis
  7. Uncontrolled heart failure
  8. Acute pulmonary embolus or pulmonary infarction
  9. Thrombosis of lower extremities
  10. Suspected dissecting aneurysm
  11. Uncontrolled asthma
  12. Pulmonary edema
  13. Room air desaturation at rest ≤85%
  14. Respiratory failure
  15. Acute noncardiopulmonary disorder that may affect exercise performance or be aggravated by exercise; and
  16. Mental impairment leading to inability to cooperate

Sites / Locations

  • Duke University Medical Center Preston Robert Tisch Brain Tumor Center

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control Group

Exercise Arm

Arm Description

These patients will continue with whatever routine exercise they already engage in.

These patients will participate in a controlled, supervised exercise program.

Outcomes

Primary Outcome Measures

Cardiorespiratory Fitness will be determined using a incremental treadmill test with 12-lead ECG monitoring.

Secondary Outcome Measures

Fasting lipids will be assessed.

Full Information

First Posted
February 12, 2008
Last Updated
October 25, 2013
Sponsor
Duke University
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1. Study Identification

Unique Protocol Identification Number
NCT00620932
Brief Title
Exercise Training Among Men With Prostate Cancer
Official Title
Feasibility of Endurance Exercise Training on Cardiovascular Risk Factors Following Radical Prostatectomy Among Men With Localized Prostate Cancer; A Community-Based Intervention
Study Type
Interventional

2. Study Status

Record Verification Date
October 2013
Overall Recruitment Status
Withdrawn
Study Start Date
January 2008 (undefined)
Primary Completion Date
November 2008 (Actual)
Study Completion Date
November 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary objective is to determine the feasibility and acceptability of a home-based endurance exercise program among men diagnosed with clinically localized prostate cancer.
Detailed Description
Approximately 40 people will take part in this study and all of these people will take part at Duke University Medical Center. Participation in this study involves the following. We will ask you to perform a cardiopulmonary exercise test (walking stress test) to determine if you have any undiagnosed cardiovascular health problems that may limit your ability to participate in an exercise training program. This test will take place at the Duke Center for Living on Duke University Campus. Complete a body composition assessment. This test is designed to determine your body fat and lean body tissue (muscle mass) percentage and will consist of you sitting quietly in a chamber with appropriate medical supervision. This test also will take place at the Duke Center for Living on Duke University Campus. Complete two questionnaires one at the beginning and one at the end that asks about how you are feeling and about your physical activity levels. The questionnaire takes about 20-30 minutes. Provide two blood samples one at the beginning and one at the end to measure levels of cardiovascular disease risk factors (cholesterol levels, c-reactive protein and insulin levels) in your blood that may be influenced by exercise. Blood collection will be drawn by medical staff at Duke University. The amount of blood drawn is approximately 2 teaspoons (10ml). We will also collect information on how much treatment you receive as well as how many and what type of side-effects you have from your medical treatment. This information will be obtained from your medical chart following the completion of your treatment. Following the successful completion of all initial tests and procedures (as described above), you will be randomly assigned (like flipping a coin) to one of the following two groups: Exercise Training Group: You will be given a customized training program aimed at increasing cardiorespiratory fitness. You will be asked to exercise 3 to 5 times per week. All sessions will include a 5 minute warm-up and 5 minute cool-down at the beginning and end of each session totaling 30-45 minutes per session. You will also receive a heart rate monitor to record each exercise session to monitor adherence and compliance. You will receive telephone calls every two weeks to provide encouragement, outline goals, and provide feedback on study progress. OR Wait-List Control Group: You will be asked to maintain your usual exercise levels during the 6 month study period. You will receive telephone calls to report your levels of exercise during the study. After study completion you will receive a heart rate monitor and an individualized exercise prescription based on your cardiorespiratory fitness test at the end of the study period (6 months).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostatectomy

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
No Intervention
Arm Description
These patients will continue with whatever routine exercise they already engage in.
Arm Title
Exercise Arm
Arm Type
Experimental
Arm Description
These patients will participate in a controlled, supervised exercise program.
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
Patients will be randomly assigned to groups and will either be given an exercise program individually tailored to them for them to participate in for 6 months or else be wait-listed for 6 months and remain on whatever exercise regimen they were already on.
Primary Outcome Measure Information:
Title
Cardiorespiratory Fitness will be determined using a incremental treadmill test with 12-lead ECG monitoring.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Fasting lipids will be assessed.
Time Frame
6 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Legal age (>18 years old) An interval of at least 6 weeks between prior radical prostatectomy and study enrollment Karnofsky performance status of at least 70% at study entry Estimated life expectancy of ≥6 months Ability to read and understand English Attending urologist approval Signed informed consent Willingness to be randomized; and No contraindications to exercise as recommended by the American Thoracic Society Exclusion Criteria: Acute myocardial infarction (6 weeks) Unstable angina Uncontrolled arrhythmias causing symptoms or hemodynamic compromise Syncope Acute endocarditis Acute myocarditis or pericarditis Uncontrolled heart failure Acute pulmonary embolus or pulmonary infarction Thrombosis of lower extremities Suspected dissecting aneurysm Uncontrolled asthma Pulmonary edema Room air desaturation at rest ≤85% Respiratory failure Acute noncardiopulmonary disorder that may affect exercise performance or be aggravated by exercise; and Mental impairment leading to inability to cooperate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lee Jones, PHd
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duke University Medical Center Preston Robert Tisch Brain Tumor Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
24315706
Citation
Jones LW, Hornsby WE, Freedland SJ, Lane A, West MJ, Moul JW, Ferrandino MN, Allen JD, Kenjale AA, Thomas SM, Herndon JE 2nd, Koontz BF, Chan JM, Khouri MG, Douglas PS, Eves ND. Effects of nonlinear aerobic training on erectile dysfunction and cardiovascular function following radical prostatectomy for clinically localized prostate cancer. Eur Urol. 2014 May;65(5):852-5. doi: 10.1016/j.eururo.2013.11.009. Epub 2013 Nov 22.
Results Reference
derived
Links:
URL
http://www.cancer.duke.edu/btc/
Description
Preston Robert Tisch Brain Tumor Center at Duke

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Exercise Training Among Men With Prostate Cancer

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