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Effects of SIT Combined with Remote Ischemic Preconditioning on Vascular Function in Young Women with Masked Obesity

B

Beijing Sport University

Status

Completed

Conditions

Vascular Function

Treatments

Behavioral: SIT combined RIPC
Behavioral: SIT

Study type

Interventional

Funder types

Other

Identifiers

NCT06664281
ESITCRIPVFYWMO

Details and patient eligibility

About

Comparison of the effects of combined Sprint Interval Training (SIT) with Remote Ischemic Preconditioning (RIPC) and SIT on vascular function in young women with masked obesity.

Full description

This is a randomized clinical trial of single-blind with 3 arms (control group, SIT group and SIT with RIPC group), in which a pre-treatment-posttest design has been used.

Enrollment

44 patients

Sex

Female

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Females aged between 18 and 30 years;
  • BMI within the normal range (18.5~24.9 kg/m²), BF% > 30%;
  • Participants with no clinically diagnosed contraindications for exercise, in good health, and not engaged in regular exercise, as determined by the health and physical activity questionnaire (based on the American College of Sports Medicine's guidelines for exercise testing and prescription).

Exclusion criteria

  • History of cardiovascular diseases, including coronary heart disease, stroke, or peripheral arterial disease diagnosed through vascular imaging techniques;
  • Currently participating in other intervention studies, including dietary, nutritional, or psychological education programs;
  • Those with regular professional training;
  • Musculoskeletal disorders that make long-term exercise interventions unsuitable.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

44 participants in 3 patient groups

sprint interval training group
Active Comparator group
Treatment:
Behavioral: SIT
sprint interval training combined with remote ischemic preconditioning group
Active Comparator group
Treatment:
Behavioral: SIT combined RIPC
Control group
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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