NCT07309237

Brief Summary

In recent years, fitness concepts have continuously evolved, with many seeking to improve and enhance their physical condition through exercise to achieve better athletic performance. Aerobic exercise not only increases lipid utilization but also boosts athletic performance. Consequently, various aerobic exercise equipment has become increasingly popular in the market. Due to the pandemic's impact in recent years, people have rarely ventured outdoors, making indoor exercise equipment increasingly popular for home workouts. Spinning has emerged as a widely adopted new fitness activity, accessible to all genders and ages. Many gyms even offer specialized spinning classes with variations in speed and resistance. However, past literature has predominantly focused on continuous-intensity spinning interventions, which do not reflect the diverse training variations found in actual spinning classes. Therefore, this study aims to investigate the effects of incorporating high-intensity interval training (HIIT) into spinning on cardiorespiratory fitness.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Aug 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 30, 2025

Completed
29 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2025

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

November 21, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

December 30, 2025

Completed
Last Updated

December 30, 2025

Status Verified

August 1, 2024

Enrollment Period

6 months

First QC Date

November 21, 2025

Last Update Submit

December 29, 2025

Conditions

Outcome Measures

Primary Outcomes (12)

  • Cardiopulmonary fitness

    VO2max (ml/kg/mL)

    Before intervention and the end of intervention at 6 weeks

  • Baseline anthropometric of the participants

    Age (yr)

    Before intervention and the end of intervention at 6 weeks

  • Cardiopulmonary fitness

    VEmax (L/min)

    Before intervention and the end of intervention at 6 weeks

  • Cardiopulmonary fitness

    maximal workload (W)

    Before intervention and the end of intervention at 6 weeks

  • Cardiopulmonary fitness

    AT% (%VO₂max)

    Before intervention and the end of intervention at 6 weeks

  • Cardiopulmonary fitness

    Resting O₂ pulse (mL·beat-¹)

    Before intervention and the end of intervention at 6 weeks

  • Cardiopulmonary fitness

    Max O₂ pulse (mL·beat-¹)

    Before intervention and the end of intervention at 6 weeks

  • Cardiopulmonary fitness

    MIP (cmH2O)

    Before intervention and the end of intervention at 6 weeks

  • Cardiopulmonary fitness

    MEP (cmH2O)

    Before intervention and the end of intervention at 6 weeks

  • Baseline anthropometric of the participants

    Height (cm)

    Before intervention and the end of intervention at 6 weeks

  • Baseline anthropometric of the participants

    Weight (kg)

    Before intervention and the end of intervention at 6 weeks

  • Baseline anthropometric of the participants

    BMI (kg/m²)

    Before intervention and the end of intervention at 6 weeks

Secondary Outcomes (8)

  • Lung function

    Before intervention and the end of intervention at 6 weeks

  • Lung functionWeight

    Before intervention and the end of intervention at 6 weeks

  • Lung function

    Before intervention and the end of intervention at 6 weeks

  • Lung function

    Before intervention and the end of intervention at 6 weeks

  • Lung function

    Before intervention and the end of intervention at 6 weeks

  • +3 more secondary outcomes

Study Arms (3)

high-intense interval training

ACTIVE COMPARATOR

Performed repeated high-intensity bouts at 75-80% of VO₂ reserve, interspersed with active recovery at 60-65% of VO₂ reserve, using a spinning bike.

Behavioral: high intense interval training

moderate-intensity continuous training

PLACEBO COMPARATOR

At approximately 70% of VO₂ reserve, using a spinning bike.

Behavioral: moderate intense continue trainingBehavioral: Control

control group

NO INTERVENTION

did not perform any exercise training

Interventions

continuously at approximately 70% of VO₂ reserve, using spinning bike

moderate-intensity continuous training
ControlBEHAVIORAL

did not perform any exercise training

moderate-intensity continuous training

performed repeated high-intensity bouts at 75-80% of VO₂ reserve, interspersed with active recovery at 60-65% of VO₂ reserve, using a spinning bike

high-intense interval training

Eligibility Criteria

Age18 Years - 25 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • no regular exercise training in the past six months
  • ability to safely perform high-intensity cycling exercise

You may not qualify if:

  • musculoskeletal limitations that prevented cycling exercise
  • recent infection
  • known cardiopulmonary disease or medical history affecting cardiovascular or respiratory function
  • smoking
  • use of medications that may influence cardiopulmonary responses to exercise
  • other contraindications to exercise testing according to the American College of Sports Medicine (ACSM) guidelines

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

No. 151, Jinxue Rd.

Kaohsiung City, Daliao, 831301, Taiwan

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
FACTORIAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 21, 2025

First Posted

December 30, 2025

Study Start

August 1, 2024

Primary Completion

January 30, 2025

Study Completion

February 28, 2025

Last Updated

December 30, 2025

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations