Exercise Intervention Metabolic Syndrome Prostate Cancer Black Men



Status:Recruiting
Conditions:Prostate Cancer, Cancer, Endocrine
Therapuetic Areas:Endocrinology, Oncology
Healthy:No
Age Range:40 - 40
Updated:4/2/2016
Start Date:July 2013
End Date:December 2017

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An Exercise Intervention on Metabolic Syndrome and Prostate Cancer Risk Among Black Men

The main purpose of this study is to examine the feasibility of an exercise intervention on
metabolic syndrome (MetS) components and biomarkers related to prostate cancer in Black men
with MetS who are at increased risk of prostate cancer.

The specific aim for the proposed study is to examine the feasibility and impact of a
6-month two-arm randomized controlled trial (RCT) on MetS components and biomarkers related
to prostate cancer in Black men with MetS. Due to the striking racial disparities of
prostate cancer, this proposal will focus on the impact of an aerobic and resistance
exercise intervention on MetS and biomarkers related to prostate cancer in Black men.
Specifically, our proposed clinical trial compares an aerobic and resistance exercise
intervention to an attention control group among Black men.

Inclusion Criteria:

1. African-American and/or Black men;

2. between the ages of 40-70 years;

3. waist circumference >40 inches (102 cm);

4. with at least two of the following: elevated BP (≥ 130/85 mmHg);

5. elevated fasting glucose (≥ 100 mg/dL), reduced HDL cholesterol (<50 mg/dL), or
elevated triglycerides (≥ 150 mg/dL);

6. sedentary defined as <60 minutes of recreation or work requiring modest PA/week;

7. be able to speak and read English;

8. able to provide meaningful consent (i.e., men with severe cognitive impairment will
be excluded);

9. have no physical limitations that prevent from exercising;

10. and have access to a television and DVD player.

Exclusion Criteria:

1. history of cancer except nonmelanoma skin cancer;

2. current enrollment in another clinical trial or weight loss program;

3. inability to commit to the intervention schedule. Prior to randomization,
participants will be required to have a signed authorization and medical clearance
from their personal physician or our nurse practitioner.
We found this trial at
1
site
Washington, District of Columbia 20003
?
mi
from
Washington,
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