NCT06962605

Brief Summary

The purpose of this study is to investigate the suitability of intermittent exercise of long and short intervals at lower intensities than HIIE on energy expenditure during and post-exercise compared to MICE, as well as determine whether similar or greater effects can be achieved for glycemic control in recreationally active adults.

Trial Health

57
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Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 22, 2025

Completed
16 days until next milestone

First Posted

Study publicly available on registry

May 8, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

June 21, 2025

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2026

Completed
Last Updated

January 26, 2026

Status Verified

January 1, 2026

Enrollment Period

10 months

First QC Date

April 22, 2025

Last Update Submit

January 23, 2026

Conditions

Keywords

Intermittent runningEnergy expenditure

Outcome Measures

Primary Outcomes (2)

  • Total energy expenditure

    Changes in total energy expenditure during 40-minutes running and 30 minutes of EPOC

    70 minutes

  • Substrate utilisation

    Changes in substrate utilisation during 40-minutes running and 30 minutes of EPOC

    70 minutes

Secondary Outcomes (2)

  • Muscle oxygen saturation

    70 minutes

  • Subjective appetite sensation

    70 minutes

Study Arms (3)

Moderate-intensity continuous running (MICE: 60% V̇O2max)

EXPERIMENTAL

Exercise

Behavioral: Moderate-intensity continuous running (MICE: 60% V̇O2max)

5-minute interval running (5MIN)

EXPERIMENTAL

Exercise

Behavioral: 5-minute interval running (5MIN)

2-minute interval running (2MIN)

EXPERIMENTAL

Exercise

Behavioral: 2-minute interval running (2MIN)

Interventions

Participants run for 40 minutes at average moderate intensity with 5-minutes slow and fast cycles where speed is increased and decreased by 20%.

5-minute interval running (5MIN)

Participants run for 40 minutes at average moderate intensity with 2-minutes slow and fast cycles where speed is increased and decreased by 20%.

2-minute interval running (2MIN)

Participants run continuously for 40 minutes at moderate intensity (60-65% V̇O2max)

Moderate-intensity continuous running (MICE: 60% V̇O2max)

Eligibility Criteria

Age20 Years - 45 Years
Sexmale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Healthy recreationally active men
  • BMI between 18.5-27 kg/m2
  • Aged between 20 to 45 years
  • Regular exercise (3 times per week and longer than 3 months) with cardio exercise longer than 30 minutes at least once a week
  • Weight stable for more than 3 months (no change in weight +/- 3%)
  • Non-shift workers and sleep at least 6.5-9 hours for the past 3 months
  • Non-smoker

You may not qualify if:

  • having any cardiovascular, metabolic or pulmonary disease (angina pectoris or uncontrolled arrhythmias)
  • suffering from infectious contagious diseases,
  • using medications that could affect metabolic responses (including anti-inflammatory medications)
  • smoking
  • heavy alcohol intake (more than 4 drinks on any day or more than 14 drinks a week).
  • undergoing special diets (e.g., intermittent fasting and/or ketogenic diets)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Taiwan Normal University

Taipei, Taiwan

RECRUITING

Central Study Contacts

Yung-Chih Chen, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Model Details: Participants will be asked to perform 4 trials in a randomized-crossover design (1) moderate-intensity continuous running (MICE: 60% V̇O2max), (2) 5-minute interval running (5MIN; 50% and 70% V̇O2max), (3) 2-minute interval running (2MIN; 50% and 70% V̇O2max).
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

April 22, 2025

First Posted

May 8, 2025

Study Start

June 21, 2025

Primary Completion

April 30, 2026

Study Completion

April 30, 2026

Last Updated

January 26, 2026

Record last verified: 2026-01

Locations