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Impact of Tele-Rehab Based Aerobic Exercise vs. Pilates Combined with the DASH Diet on Metabolic Syndrome: A Comparative Study

A Comparative Analysis of the Effects of Aerobic Exercise versus Pilates in a Tele- Rehab Program, combined with the DASH Diet on Metabolic Syndrome. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085441
Enrollment
34
Registered
2025-04-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E70-E88- Metabolic disorders

Interventions

Intervention1: Aerobic Exercises with DASH Diet: Aerobic Exercises with DASH Diet Performed by Metabolic Syndrome Patients for 5 days per week for 6 weeks Control Intervention1: Pilates with DASH Diet

Sponsors

Gurugram University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i. Must meet at least three of the diagnostic criteria [BMI more than 25kg per m2, BP more than 120(SBP) and 80 (DBP), HBA1C more than or equal to 5.7mmol per mol, Total Cholesterol more than or equal to 200mg/dl] ii. Participants aged between 18 and 55 years. iii. Sedentary or minimally active individuals (defined as light or moderate exercise for up to 30 minutes, no more than twice per week, in past 90 days). iv. Willingness to follow the DASH diet as prescribed during the study period. v. Medically stable and able to participate in moderate-intensity physical activity, as determined by a physician.

Exclusion criteria

Exclusion criteria: i. Participants who are not willing to provide informed written consent to participate in the study. ii. Participants engaged in structured exercise program and not adhering to standardized medication regimen for metabolic syndrome. iii. Musculoskeletal, neurological, or other conditions that prevent safe participation in aerobic exercise or Pilates. iv. Pregnancy, breastfeeding, or intention to conceive during the study period. v. Participation in another clinical trial within the last 30 days that could interfere with this study.

Design outcomes

Primary

MeasureTime frame
Blood Pressure High Density Lipoproteins Fasting Blood Sugar Non-Fasting Blood SugarTimepoint: 6 Weeks

Secondary

MeasureTime frame
Body Mass Index Waist to Hip RatioTimepoint: 6 weeks

Countries

India

Contacts

Public ContactHarshita

Gurugram University

sonia@gurugramuniversity.ac.in9416414362

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026