Aerobic Plus Resistance Training and Insulin Sensitivity in African American Men (ARTIIS)

Pennington Biomedical Research Center

Status

Completed

Conditions

Insulin Resistance

Type 2 Diabetes

Treatments

Behavioral: Aerobic Plus Resistance Training Group

Behavioral: Control Group

Study type

Interventional

Funder types

Other

Identifiers

NCT01787617

PBRC 11038

Details and patient eligibility

About

The purpose of this study is to investigate the effect of an exercise training intervention on the ability of African American males to use insulin properly. Insulin is a hormone that helps the body use glucose.

Full description

This study is designed to assess the effect of exercise training on insulin resistance in African American males. African American males have higher rates of diabetes and lower levels of fitness when compared to Caucasian males. A project such as this is necessary because there is evidence to show that exercise training can reduce the risk of developing diabetes, though no studies have been conducted in African American males. In addition, ARTIIS will test the effect adhering to the 2008 Physical Activity Guidelines for Americans (150 minutes of moderate intensity aerobic activity and 2 days of 20 minutes of muscular strength activity), on insulin resistance in African American men. This study will provide important information that can either strengthen or refine current physical activity recommendations. Furthermore, this intervention will be delivered through community facilities in order to increase the likelihood that the intervention will be sustainable.

Enrollment

113 patients

Sex

Male

Ages

35 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

You completed the three run-in screening visits.
You self-identify as a male of African descent.
You are 35 to 70 years of age.
You have a BMI (ratio of your height to your weight) greater than or equal to 25.0 kg/m2 and less than or equal to 40 kg/m2.
You have a family history of diabetes.
You are not currently physically active for 20 minutes each time for 3 or more days per week for the last 6 months. You are not participating in regular muscle building exercise.
You are willing to give informed consent, willing to be randomized to either the healthy living intervention group or the aerobic plus resistance training exercise group, and willing to follow the protocol for the group to which you have been assigned.

Exclusion criteria

You drink more than 14 alcoholic drinks per week.
You plan to move out of the study area within the next 6 months, or plan to be out of the study area for more than 4 weeks during the course of the study.
You have another member of your household participating in the study.
You have serious health conditions that would interfere with the intervention goals
History of cardiovascular disease (CVD) or disorders and are not under the care of a physician to treat the condition, or fail to provide written documentation from your physician indicating that the physician approves of your entering the study
Have high blood pressure (greater than 155/99 mmHg) and are not under the care of a physician to treat the condition or fail to provide written documentation from your physician indicating that the physician approves of your entering the study
Have a previous diagnosis of diabetes (Type 1 or 2) or a fasting plasma glucose of >125 mg/dl
Have elevated bad cholesterol (greater than or equal to 190mg/dl) or triglycerides (great than or equal to 300) and are not under the care of a physician to treat the condition or fail to provide written documentation from your physician indicating that the physician approves of you entering the study
Are currently taking medications for diabetes or chronic steroid use
Have chronic or recurrent respiratory, gastrointestinal, neuromuscular, neurological or psychiatric conditions
Have had cancer requiring treatment in the past 5 years, expect for non-melanoma skin cancers or cancers that have clearly been cured or in the option of the investigator carry an excellent prognosis (e.g., Stage 1 cervical cancer)
Have autoimmune or collagen vascular diseases
Have immunodeficiency diseases or HIV
You have any other medical, psychiatric, or behavioral factors that in the judgment of the Principal Investigator are life-threatening or that may interfere with study participation or the ability to follow the intervention protocol.