Dance Dance Revolution (DDR) in Type 2 Diabetes
Primary Purpose
Type 2 Diabetes Mellitus
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
DDR
Treadmill
Sponsored by

About this trial
This is an interventional treatment trial for Type 2 Diabetes Mellitus focused on measuring Exercise, Video game, Type 2 diabetes, Dance
Eligibility Criteria
Inclusion Criteria:
- Age 18 to 65 inclusive
- Diagnosed type 2 diabetes mellitus (by ADA diagnostic criteria) for at least 1 year
- On stable doses of oral anti-hyperglycemic medications for at least 3 months (i.e., sulfonylureas, metformin, thiazolidinediones, and/or DPP-4 inhibitors; GLP-1 analogues may also be permitted)
- Hemoglobin A1c level between 7.5% and 9.0% inclusive
- Body mass index (BMI) between 25.0 and 40.0 kg/m2 inclusive
- Able to engage in a regular program of mild-to-moderate intensity physical activity
- Subjects not currently engaged in any regimented exercise program outside of the usual activities of daily living that is intended to achieve metabolic changes (e.g., weight loss, athletic training, etc.)
- Able to give informed consent and cooperate with all necessary procedures of the study
Exclusion Criteria:
- Any contraindications to a regular program of mild-to-moderate intensity exercise, or any cardiovascular, pulmonary, orthopedic, rheumatological or neurological conditions that may, in the opinion of the investigators, interfere with the subject's optimal participation in a regular exercise program, interfere with the quality of the data collected from the subject, or make a regular exercise program potentially hazardous
- Diabetes mellitus currently being treated with insulin and/or pramlintide
- Screening fasting plasma glucose (FPG) 300 mg/dL or greater or symptoms of hyperglycemia (polyuria, polydipsia); screening FPG < 60 mg dL, or a history of symptomatic hypoglycemia averaging more than once per day; or any other history suggestive of erratic glucose control
- Screening fasting triglycerides 500 mg/dL or greater; or LDL-cholesterol 200 mg/dL or greater; screening blood pressure averaging 180 mm Hg or greater systolic or 100 mm Hg or greater diastolic
- Subjects currently engaged in any regimented exercise program outside of the usual activities of daily living that is intended to achieve metabolic changes (e.g., weight loss, athletic training, etc.); any such activities occurring on a sporadic basis may still disqualify the subject, depending upon its frequency, to be judged at the discretion of the PI. Subjects must maintain their usual occupational and other routine daily activities during the study at a reasonably constant level.
- Subjects who routinely engage in DDR, either at home or video game arcades; "occasional" participation in DDR may still disqualify the subject, depending upon the frequency of participation, to be judged at the discretion of the PI
- Changing doses of any concurrent medications that are known to alter the study's outcomes (e.g., oral anti-hyperglycemic agents, lipid-lowering agents, weight loss agents, anti-hypertensive agents, systemic glucocorticoids, thyroid medications, hormone replacement therapies, oral contraceptives, etc.) or the anticipated need to start any of these medications; such medications taken concurrently must remain at constant dosages throughout the study.
- Past history of clinically significant dysfunction of other organ systems (e.g., known hepatic disease or hepatic transaminase levels greater than 3X the upper limit of the normal range other than steatohepatitis; known renal dysfunction or creatinine level 1.5 mg/dL or greater; past history of malignancies excluding cutaneous basal cell carcinoma; known chronic infections including HIV, endocrinopathies such as untreated thyroid disease, adrenal disease, or pituitary dysfunction, etc.), or any recent surgeries that preclude regular exercise, in the opinion of the investigators
- Active hemolytic anemia, known hemoglobinopathies, or any other state of accelerated RBC turnover that may alter the accuracy of the HbA1c measurement
- Pregnancy or lactation
Sites / Locations
- Charles Drew University of Medicine and Science
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
DDR
Treadmill
Arm Description
"Dance Dance Revolution" (DDR) Exergaming
Treadmill exercise
Outcomes
Primary Outcome Measures
Hemoglobin A1c change from baseline
Secondary Outcome Measures
Body mass index change from baseline
Body composition change from baseline
Fasting lipid profile change from baseline
Blood pressure change from baseline
Fasting plasma glucose change from baseline
HOMA-IR index change from baseline
Aerobic fitness change from baseline
Mean daily caloric intake
Mean total exercise time
Mean exercise energy expenditure
Behavioral questionnaires change from baseline
All adverse events
Full Information
NCT ID
NCT00851019
First Posted
February 23, 2009
Last Updated
March 25, 2013
Sponsor
Charles Drew University of Medicine and Science
Collaborators
American Diabetes Association
1. Study Identification
Unique Protocol Identification Number
NCT00851019
Brief Title
Dance Dance Revolution (DDR) in Type 2 Diabetes
Official Title
Dance Dance Revolution (DDR) Exergaming in Adults With Type 2 Diabetes Mellitus
Study Type
Interventional
2. Study Status
Record Verification Date
March 2013
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
July 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Charles Drew University of Medicine and Science
Collaborators
American Diabetes Association
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Regular physical activity is important for the treatment of type 2 diabetes, but it is often not sustained for many reasons, including lack of interest. New video games that involve physical movement ("exergames") may help in this regard. This study will compare the "exergame" "Dance Dance Revolution" (DDR) with traditional treadmill exercise on blood sugar control among sedentary, overweight or obese adults with type 2 diabetes.
Detailed Description
This study is a randomized, controlled trial of a 3-month ad libitum program of the "exergame" "Dance Dance Revolution" (DDR) versus traditional treadmill exercise. Each group of subjects will be assessed at baseline, and then assigned exclusively to one of the two exercise modalities. Subjects will be free to attend exercise sessions in their assigned exercise modality at the exercise facility, at a frequency, duration and intensity of their own choosing with minimal staff supervision, for a period of exactly 90 days; adoption of new exercise programs outside of the study will be prohibited. Dosages of any concurrent medications will be maintained constant, and all subjects will receive standardized nutrition counseling.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus
Keywords
Exercise, Video game, Type 2 diabetes, Dance
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
76 (Actual)
8. Arms, Groups, and Interventions
Arm Title
DDR
Arm Type
Experimental
Arm Description
"Dance Dance Revolution" (DDR) Exergaming
Arm Title
Treadmill
Arm Type
Active Comparator
Arm Description
Treadmill exercise
Intervention Type
Behavioral
Intervention Name(s)
DDR
Intervention Description
Ad libitum attendance to engage in "Dance Dance Revolution" (DDR) Exergaming, for a 3-month period
Intervention Type
Behavioral
Intervention Name(s)
Treadmill
Intervention Description
Ad libitum attendance to engage in treadmill exercise, for a 3-month period
Primary Outcome Measure Information:
Title
Hemoglobin A1c change from baseline
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Body mass index change from baseline
Time Frame
3 months
Title
Body composition change from baseline
Time Frame
3 months
Title
Fasting lipid profile change from baseline
Time Frame
3 months
Title
Blood pressure change from baseline
Time Frame
3 months
Title
Fasting plasma glucose change from baseline
Time Frame
3 months
Title
HOMA-IR index change from baseline
Time Frame
3 months
Title
Aerobic fitness change from baseline
Time Frame
3 months
Title
Mean daily caloric intake
Time Frame
3 months
Title
Mean total exercise time
Time Frame
3 months
Title
Mean exercise energy expenditure
Time Frame
3 months
Title
Behavioral questionnaires change from baseline
Time Frame
3 months
Title
All adverse events
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18 to 65 inclusive
Diagnosed type 2 diabetes mellitus (by ADA diagnostic criteria) for at least 1 year
On stable doses of oral anti-hyperglycemic medications for at least 3 months (i.e., sulfonylureas, metformin, thiazolidinediones, and/or DPP-4 inhibitors; GLP-1 analogues may also be permitted)
Hemoglobin A1c level between 7.5% and 9.0% inclusive
Body mass index (BMI) between 25.0 and 40.0 kg/m2 inclusive
Able to engage in a regular program of mild-to-moderate intensity physical activity
Subjects not currently engaged in any regimented exercise program outside of the usual activities of daily living that is intended to achieve metabolic changes (e.g., weight loss, athletic training, etc.)
Able to give informed consent and cooperate with all necessary procedures of the study
Exclusion Criteria:
Any contraindications to a regular program of mild-to-moderate intensity exercise, or any cardiovascular, pulmonary, orthopedic, rheumatological or neurological conditions that may, in the opinion of the investigators, interfere with the subject's optimal participation in a regular exercise program, interfere with the quality of the data collected from the subject, or make a regular exercise program potentially hazardous
Diabetes mellitus currently being treated with insulin and/or pramlintide
Screening fasting plasma glucose (FPG) 300 mg/dL or greater or symptoms of hyperglycemia (polyuria, polydipsia); screening FPG < 60 mg dL, or a history of symptomatic hypoglycemia averaging more than once per day; or any other history suggestive of erratic glucose control
Screening fasting triglycerides 500 mg/dL or greater; or LDL-cholesterol 200 mg/dL or greater; screening blood pressure averaging 180 mm Hg or greater systolic or 100 mm Hg or greater diastolic
Subjects currently engaged in any regimented exercise program outside of the usual activities of daily living that is intended to achieve metabolic changes (e.g., weight loss, athletic training, etc.); any such activities occurring on a sporadic basis may still disqualify the subject, depending upon its frequency, to be judged at the discretion of the PI. Subjects must maintain their usual occupational and other routine daily activities during the study at a reasonably constant level.
Subjects who routinely engage in DDR, either at home or video game arcades; "occasional" participation in DDR may still disqualify the subject, depending upon the frequency of participation, to be judged at the discretion of the PI
Changing doses of any concurrent medications that are known to alter the study's outcomes (e.g., oral anti-hyperglycemic agents, lipid-lowering agents, weight loss agents, anti-hypertensive agents, systemic glucocorticoids, thyroid medications, hormone replacement therapies, oral contraceptives, etc.) or the anticipated need to start any of these medications; such medications taken concurrently must remain at constant dosages throughout the study.
Past history of clinically significant dysfunction of other organ systems (e.g., known hepatic disease or hepatic transaminase levels greater than 3X the upper limit of the normal range other than steatohepatitis; known renal dysfunction or creatinine level 1.5 mg/dL or greater; past history of malignancies excluding cutaneous basal cell carcinoma; known chronic infections including HIV, endocrinopathies such as untreated thyroid disease, adrenal disease, or pituitary dysfunction, etc.), or any recent surgeries that preclude regular exercise, in the opinion of the investigators
Active hemolytic anemia, known hemoglobinopathies, or any other state of accelerated RBC turnover that may alter the accuracy of the HbA1c measurement
Pregnancy or lactation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stanley Hsia, MD
Organizational Affiliation
Charles Drew University of Medicine and Science
Official's Role
Principal Investigator
Facility Information:
Facility Name
Charles Drew University of Medicine and Science
City
Los Angeles
State/Province
California
ZIP/Postal Code
90059
Country
United States
12. IPD Sharing Statement
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Dance Dance Revolution (DDR) in Type 2 Diabetes
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