About this trial
The goal of this clinical trial is to learn whether Waltz dance can improve cardiometabolic and bone health in sedentary women aged 45-65 with abnormal lipid levels. The main questions it aims to answer are:
Can Waltz dance improve blood lipid profiles, including total cholesterol, triglycerides, HDL-C, and LDL-C? Can it improve body composition, cardiorespiratory fitness, vascular function, and bone mineral density? Researchers will compare a Waltz dance group with a control group that maintains their usual lifestyle to see if the dance intervention leads to better health outcomes.
Participants will:
Attend supervised Waltz dance classes three times a week for 12 weeks, each session lasting 105 minutes.
Complete physical tests and blood draws before and after the program to measure changes in lipid levels, body composition, fitness, and bone density.
Wear an accelerometer to monitor energy expenditure and physical activity during the program.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Female participants aged between 45 and 65 years.
Diagnosed with dyslipidemia (based on clinical lipid profile: TC ≥ 6.2 mmol/L, TG ≥ 2.3 mmol/L, LDL-C ≥ 4.1 mmol/L, or HDL-C < 1.0 mmol/L).
Sedentary lifestyle (less than 60 minutes of structured physical activity per week in the last 6 months).
Able to participate safely in moderate-intensity exercise as confirmed by a medical evaluation.
Disqualifiers
Diagnosis of cardiovascular disease requiring medical supervision during exercise (e.g., unstable angina, recent myocardial infarction).
Severe musculoskeletal disorders (e.g., advanced osteoarthritis, recent fractures) limiting mobility or physical activity.
Neurological or cognitive disorders affecting motor function or communication.
Uncontrolled hypertension (SBP ≥ 160 mmHg or DBP ≥ 100 mmHg at rest).
Trial design
Parallel
Treatments tested in this trial
Waltz Dance
BehavioralParticipants in this arm will receive a structured Waltz dance intervention as moderate-intensity aerobic exercise. The program consists of 3 supervised sessions per week for 12 weeks, each lasting 105 minutes. Each session includes a 5-minute warm-up, 50 minutes of solo and partner Waltz practice, a 5-minute rest, 40 minutes of choreographed combinations, and a 5-minute cool-down. The dance routines are progressive and designed to improve cardiovascular fitness, coordination, and balance. Exercise intensity is maintained at 50-70% of estimated maximum heart rate, with music tempo and movement complexity adjusted as needed. Physical activity is monitored using accelerometers to ensure target intensity is achieved.
Treatment groups
Trial outcomes
Primary outcomes
Total Cholesterol (TC) Level
Total cholesterol (TC) levels will be measured using fasting venous blood samples collected at baseline and after 12 weeks of intervention. Blood will be drawn in the morning after at least 8 hours of fasting. Serum will be analyzed in a certified laboratory using standard enzymatic colorimetric assays. TC is expressed in milligrams per deciliter (mg/dL). Elevated TC is a known risk factor for cardiovascular disease. Changes from baseline to post-intervention will be calculated.
Triglycerides (TG) Level
Triglyceride (TG) levels will be assessed through fasting blood samples taken before and after the 12-week intervention. Samples will be processed using standardized laboratory techniques. TG is measured in mg/dL and high levels are associated with increased risk for metabolic and cardiovascular conditions. This outcome measures the change in TG levels between baseline and the end of the study.
High-Density Lipoprotein Cholesterol (HDL-C) Level
HDL-C will be measured in serum obtained from fasting venous blood samples collected at baseline and 12 weeks. HDL-C is commonly known as "good" cholesterol due to its protective effect against cardiovascular disease. Standard enzymatic methods will be used for quantification. The change in HDL-C from baseline to post-intervention will be analyzed.
Low-Density Lipoprotein Cholesterol (LDL-C) Level
LDL-C will be measured from fasting blood samples collected at the beginning and end of the 12-week intervention. LDL-C, often referred to as "bad" cholesterol, is a key risk factor for atherosclerosis and cardiovascular disease. The value will be determined using direct measurement or calculation by the Friedewald formula. Results will be reported in mg/dL, and changes from baseline to week 12 will be evaluated.
Secondary outcomes
Systolic and Diastolic Blood Pressure and Pulse Pressure (mmHg)
Resting systolic blood pressure (SBP), diastolic blood pressure (DBP), and pulse pressure (PP = SBP - DBP) will be measured using an automated upper-arm blood pressure monitor (e.g., Omron HEM-7136). Participants will rest quietly in a seated position for at least 5 minutes before three measurements are taken on the right arm. The average of the three readings will be recorded.
Pulse Wave Velocity (m/s)
Carotid-femoral pulse wave velocity (cfPWV), an indicator of arterial stiffness and vascular function, will be measured using a validated device (e.g., Complior Analyse). Measurements will be taken while participants are in the supine position after 10 minutes of rest. Higher values indicate increased arterial stiffness.
Ankle-Brachial Index (ABI)
ABI is calculated as the ratio of the systolic blood pressure at the ankle (posterior tibial artery) to that in the arm (brachial artery), using a handheld Doppler ultrasound device. Measurements will be taken bilaterally (left and right sides), and the lower of the two values will be used for analysis. ABI values typically range from 0.00 to 2.00, with higher scores indicating better arterial perfusion. Values below 0.90 may indicate peripheral arterial disease (PAD), while values above 1.30 may suggest arterial stiffness or calcification.
Cardiorespiratory Fitness - Maximal Oxygen Uptake (VO2max)
VO2max will be assessed via a graded exercise treadmill test using the Bruce protocol. Participants will wear a metabolic analyzer (e.g., Cortex MetaLyzer 3B) to measure oxygen consumption. The highest VO2 achieved before exhaustion will be recorded.
Other outcomes
Weight
Body weight will be measured using a calibrated digital scale with participants in light clothing, without shoes.Unit of Measure: Kilograms (kg).Higher values: May indicate weight gain; lower values may suggest weight loss.
Bone Mineral Density (BMD)
BMD will be measured at the lumbar spine (L1-L4) and femoral neck using dual-energy X-ray absorptiometry (DXA; e.g., Hologic Discovery A). Results will be expressed as grams per square centimeter (g/cm²), representing the mineral density of bone tissue.Unit of Measure: g/cm².Higher values: Indicate better bone mineral density.
Body Mass Index (BMI)
BMI will be calculated as weight in kilograms divided by the square of height in meters (kg/m²), using measured height and weight. It is a standard measure of body fatness.Unit of Measure: kg/m².Higher values: Indicate greater body mass.
Body Fat Percentage
Body fat percentage will be assessed using dual-energy X-ray absorptiometry (DXA; e.g., Hologic Discovery A). It represents the proportion of fat to total body mass.Unit of Measure: Percent (%).Higher values: Indicate greater fat accumulation.
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