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The benefits of combining Pilates and HIIT for competitive athletes

Effect of Pilates and HIIT on selected physiological, biochemical and psychological variables among sports players

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10727055
Enrollment
80
Registered
2026-07-31
Start date
2022-12-15
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

A Pilates and high-intensity interval training (HIIT) program for healthy recreational sports players. Other

Interventions

Participants were recruited from recreational sports players and the investigator's health studio clients after eligibility screening and obtaining written informed consent. The two intervention group

Sponsors

SRM University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: 1. Healthy recreational sports players 2. Age 18–25 years 3. Both males and females (if applicable to your study; otherwise specify only males or only females) 4. Willing to provide written informed consent 5. Able to participate in a 16-week combined Pilates and high-intensity interval training (HIIT) program 6. Free from cardiovascular, neurological, musculoskeletal, or metabolic disorders that would limit exercise participation

Exclusion criteria

Exclusion criteria: 1. Individuals younger than 18 years or older than 25 years 2. History of cardiovascular, respiratory, neurological, musculoskeletal, or metabolic disorders that could affect exercise participation 3. Current injury or illness preventing participation in the exercise program 4. Participation in another structured exercise training or clinical research program during the study period 5. Use of medications known to significantly affect metabolic, hormonal, or cardiovascular responses 6. Pregnancy (if female participants were included) 7. Failure to provide written informed consent or inability to comply with the study protocol

Design outcomes

Primary

MeasureTime frame
Aerobic capacity (VO2max) measured using a graded exercise test (mL/kg/min) at baseline (Week 0) and after completion of the 16-week intervention (Week 16);Serum cortisol levels measured using a laboratory biochemical analysis at baseline and Week 16

Countries

India

Contacts

Public ContactLavanya Dhanasekaran Lalitha
ld3958@srmist.edu.in+91 09884870345

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Aug 25, 2026