Dance Dance Revolution (DDR) in Type 2 Diabetes
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ClinicalTrials.gov Identifier: NCT00851019 |
Recruitment Status :
Completed
First Posted : February 25, 2009
Last Update Posted : March 27, 2013
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Type 2 Diabetes Mellitus | Behavioral: DDR Behavioral: Treadmill | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 76 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Dance Dance Revolution (DDR) Exergaming in Adults With Type 2 Diabetes Mellitus |
Study Start Date : | February 2009 |
Actual Primary Completion Date : | July 2012 |
Actual Study Completion Date : | July 2012 |

Arm | Intervention/treatment |
---|---|
Experimental: DDR
"Dance Dance Revolution" (DDR) Exergaming
|
Behavioral: DDR
Ad libitum attendance to engage in "Dance Dance Revolution" (DDR) Exergaming, for a 3-month period |
Active Comparator: Treadmill
Treadmill exercise
|
Behavioral: Treadmill
Ad libitum attendance to engage in treadmill exercise, for a 3-month period |
- Hemoglobin A1c change from baseline [ Time Frame: 3 months ]
- Body mass index change from baseline [ Time Frame: 3 months ]
- Body composition change from baseline [ Time Frame: 3 months ]
- Fasting lipid profile change from baseline [ Time Frame: 3 months ]
- Blood pressure change from baseline [ Time Frame: 3 months ]
- Fasting plasma glucose change from baseline [ Time Frame: 3 months ]
- HOMA-IR index change from baseline [ Time Frame: 3 months ]
- Aerobic fitness change from baseline [ Time Frame: 3 months ]
- Mean daily caloric intake [ Time Frame: 3 months ]
- Mean total exercise time [ Time Frame: 3 months ]
- Mean exercise energy expenditure [ Time Frame: 3 months ]
- Behavioral questionnaires change from baseline [ Time Frame: 3 months ]
- All adverse events [ Time Frame: 3 months ]

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Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
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

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00851019
United States, California | |
Charles Drew University of Medicine and Science | |
Los Angeles, California, United States, 90059 |
Principal Investigator: | Stanley Hsia, MD | Charles Drew University of Medicine and Science |
Responsible Party: | Charles Drew University of Medicine and Science |
ClinicalTrials.gov Identifier: | NCT00851019 |
Other Study ID Numbers: |
08-08-2177 |
First Posted: | February 25, 2009 Key Record Dates |
Last Update Posted: | March 27, 2013 |
Last Verified: | March 2013 |
Exercise Video game Type 2 diabetes Dance |
Diabetes Mellitus Diabetes Mellitus, Type 2 Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases |