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Regulation of HIIT Combined with IET on Vascular Function in Young Women with Normal Weight Obesity

Regulation of HIIT Combined with IET on Vascular Function in Young Women with Normal Weight Obesity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06556875
Enrollment
45
Registered
2024-08-16
Start date
2023-02-23
Completion date
2023-12-30
Last updated
2024-10-28

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

Conditions

Normal Weight Obesity

Keywords

isometric exercise training, high-intensity interval training, normal weight obesity, vascular fitness

Brief summary

Comparison of the effects of combined IET with HIIT and HIIT on vascular function in young NWO women.

Detailed description

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

Interventions

BEHAVIORALHIIT

high intensity interval training

BEHAVIORALHIIT combined IET

high intensity interval training combined with isometric exercise training

Sponsors

Beijing Sport University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Female, aged between 18 and 30 years old; * BMI between 18.5 and 24.9 kg/m2 with a BF% \> 30% (normal weight obesity determination criteria); * exercise capacity to complete the exercise programme.

Exclusion criteria

* Acute or chronic musculoskeletal disorders, cardiovascular diseases, etc. that prevented training; * other diseases (such as diabetes, etc.) that had a great impact on physical condition; * bad habits (such as smoking, drinking, etc.); * and unstable body weight (up and down fluctuations of more than 2.5 kg) in the 3 months before the experiment.

Design outcomes

Primary

MeasureTime frameDescription
Intima-Media Thickness (IMT)8 weeksThe subjects were required to sit still for 5~10 minutes before the test, and the carotid artery structural and functional parameters were recorded using a GE vivid 7 colour ultrasound instrument from the United States as follows: the subjects were required to lie in the supine position, and the probe was used to sweep longitudinally along the outer edge of the sternocleidomastoid muscle, and the maximal Intima-media thickness (IMT) was measured. Changes in Intima media thickness before and after intervention.
Flow-Mediated Dilation (FMD)8 weeksVascular endothelial function was measured with a Japanese-made UNEX EF vascular endothelial function tester. Pressure was applied on top of the resting blood pressure and the ischaemic process was performed for 5 min. At the end of the ischaemic process, the pressure band was removed and flow-mediated dilation (FMD) of the brachial artery was calculated. Changes in Flow-mediated dilation before and after Intervention

Secondary

MeasureTime frameDescription
Blood Pressure (BP)8 weeksQuiet blood pressure: Systolic and diastolic blood pressures are measured using a standard mercury sphygmomanometer. Changes in blood pressure before and after intervention, including systolic blood pressure, diastolic blood pressure, and pulse pressure difference.
Body Composition Indicators8 weeksBody composition indicators analysis was assessed using DXA. Body composition indicators include: fat mass(kg), lean body mass(kg), percentage of body fat(%).
Volume Oxygen Maximum (VO2max)8 weeksDuring the test, gradually increasing loads were performed using the Bruce running table protocol, and gas metabolism metrics were obtained at each stage of exercise using a portable Cortex-3B gas metabolism analyser. Changes in Volume oxygen maximum before and after Intervention.
Pulse Wave Velocity (PWV) and ankle brachial index (ABI)8 weeksThe testing instrument is Omron Atherosclerosis Tester (BP-203RPEIII). During the test, the subjects need to expose their limbs, lie flat on the bed, and keep their bodies relaxed. At the same time, they need to tie cuffs around their limbs to avoid any physical movement and ensure the accuracy of the test results. The unit of PWV is (cm/s), and ABI is a numerical value. Changes in Pulse wave velocity and ankle brachial index before and after Intervention.
Body Mass Index (BMI)8 weeksIs calculated from the formula, Weight (kg) / Height2 (m2), whose unit is kg/m2. It is a rough indicator of total body fat. Changes in Body mass index before and after Intervention.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026