NCT07180550

Brief Summary

Moderate-intensity physical exercise is widely recognized for its health benefits, yet time constraints limit adherence. High-intensity interval training (HIIT) has gained popularity as a more time-efficient alternative, eliciting significant cardiovascular, respiratory, metabolic, and neuromuscular responses. More recently, functional strength exercises have been integrated into high-intensity training, leading to high-intensity functional training (HIFT) and moderate-intensity functional training (MIFT). However, the acute physiological responses to these modalities remain underexplored compared to traditional HIIT (running or cycling) and strength training. This study aims to assess and compare the acute cardiovascular, metabolic, and neuromuscular responses of HIFT, MIFT, HIIT, and traditional strength training in healthy, physically active adults to inform their potential application in special populations.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
27

participants targeted

Target at below P25 for not_applicable

Timeline
9mo left

Started Oct 2025

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

Study Progress44%
Oct 2025Jan 2027

First Submitted

Initial submission to the registry

September 9, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

September 18, 2025

Completed
24 days until next milestone

Study Start

First participant enrolled

October 12, 2025

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2027

Last Updated

March 10, 2026

Status Verified

March 1, 2026

Enrollment Period

1.2 years

First QC Date

September 9, 2025

Last Update Submit

March 9, 2026

Conditions

Keywords

Metabolic demandOxygen consumptionHeart rate variabilityInterval trainingStrength training

Outcome Measures

Primary Outcomes (1)

  • Heart rate variability

    The heart rate variability (HRV) of the participants will be assessed by monitoring their heart rate, which reflects the variation in the intervals between heartbeats (R-R intervals). This measure is a useful tool in monitoring patient health, as it estimates the balance between the sympathetic and parasympathetic activity of the autonomic nervous system. To evaluate heart rate variability, a Polar H10 heart rate monitor (Polar Electro Oy, Kempele, Finland) and a mobile application, specifically Elite HRV, will be used. Heart rate variability will be monitored daily during the week leading up to the initial assessment visits. Participants will be instructed to take the measurement for the first 5 minutes upon waking and while fasting. Subsequently, heart rate variability will be assessed immediately before each training condition, as well as immediately after, at 2, 24, 48, and 72 hours after finishing each training condition.

    Week 0 (baseline), Weeks 1-4 (during intervention and 24, 48, and 72 hours post-intervention)

Secondary Outcomes (6)

  • Post-exercise oxygen debt

    Weeks 2-4 (after every intervention session)

  • Delayed onset muscle soreness

    Weeks 2-4 (24, 48, and 72 hours post-intervention)

  • Satisfaction with the type of training

    Weeks 2-4 (right after every intervention session and 24 hours post-intervention)

  • Subjective post-exercise fatigue

    Weeks 2-4 (right after every intervention session and 24 hours post-intervention)

  • Perceived effort

    Weeks 2-4 (right after every intervention session and 24, 48, and 72 hours post-intervention)

  • +1 more secondary outcomes

Other Outcomes (11)

  • Physical activity levels

    Week 0 (baseline)

  • Cardiorespiratory fitness

    Week 1 (baseline)

  • Cardiorespiratory fitness

    Week 1 (baseline)

  • +8 more other outcomes

Study Arms (6)

High-intensity interval training (running)

EXPERIMENTAL

Participants will perform a high-intensity interval training based on six sets of 2-minute runs at an intensity of 90-95% of the maximal aerobic speed (MAS) on a treadmill. The recovery between each set will be 2 minutes, during which the subject will walk at an intensity of 50-60% of MAS.

Other: High-intensity interval training, running

High-intensity interval training (cycling)

EXPERIMENTAL

Participants will perform a high-intensity interval training based on six sets of 2-minute cycling will be performed at an intensity of 90-95% of the maximal heart rate on a stationary bike. The recovery between each set will be 2 minutes, during which the subject will cycle at an intensity of 50-60% of maximal heart rate.

Other: High-intensity interval training, cycling

High-intensity functional training

EXPERIMENTAL

Participants will perform a high-intensity functional training based on three sets of six repetitions will be performed at 80% of the one repetition maximum (1-RM) for six exercises. The recovery between exercises will be the minimum time required to switch from one exercise to the next, and between sets, it will be two minutes. Participants will be instructed to move the load as quickly as possible during each repetition.

Other: High-intensity functional training

Moderate-intensity functional training

EXPERIMENTAL

Participants will perform a moderate-intensity functional training based on three sets of six repetitions will be performed at 60% of the 1-RM for six exercises. The recovery between exercises will be the minimum time required to switch from one exercise to the next, and between sets, it will be two minutes. Participants will be instructed to move the load as quickly as possible during each repetition.

Other: Moderate-intensity functional training

High-intensity traditional training

EXPERIMENTAL

Participants will perform a high-intensity traditional training based on three sets of six repetitions will be performed at 80% of the 1-RM for six exercises. The recovery after each set will be two minutes of passive rest. Participants will be instructed to move the load as quickly as possible during each repetition.

Other: High intensity traditional strength training

Moderate-intensity traditional training

EXPERIMENTAL

Participants will perform a high-intensity traditional training based on three sets of six repetitions will be performed at 60% of the 1-RM for six exercises. The recovery after each set will be two minutes of passive rest. Participants will be instructed to move the load as quickly as possible during each repetition.

Other: Moderate intensity traditional strength training

Interventions

Six sets of 2-minute runs will be performed at an intensity of 90-95% of the maximal aerobic speed (MAS) on a treadmill. The recovery between each set will be 2 minutes, during which the subject will walk at an intensity of 50-60% of MAS.

High-intensity interval training (running)

Six sets of 2-minute cycling will be performed at an intensity of 90-95% of the maximal heart rate on a stationary bike. The recovery between each set will be 2 minutes, during which the subject will cycle at an intensity of 50-60% of maximal heart rate.

High-intensity interval training (cycling)

Three sets of six repetitions will be performed at 80% of the one repetition-maximum (1-RM) for six exercises. The recovery between exercises will be the minimum time required to switch from one exercise to the next, and between sets, it will be two minutes. Participants will be instructed to move the load as quickly as possible during each repetition.

High-intensity functional training

Three sets of six repetitions will be performed at 60% of the 1-RM for six exercises. The recovery between exercises will be the minimum time required to switch from one exercise to the next, and between sets, it will be two minutes. Participants will be instructed to move the load as quickly as possible during each repetition.

Moderate-intensity functional training

Three sets of six repetitions will be performed at 60% of the 1-RM for six exercises. The recovery after each set will be two minutes of passive rest. Participants will be instructed to move the load as quickly as possible during each repetition.

Moderate-intensity traditional training

Three sets of six repetitions will be performed at 80% of the 1-RM for six exercises. The recovery after each set will be two minutes of passive rest. Participants will be instructed to move the load as quickly as possible during each repetition.

High-intensity traditional training

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Be 18 years of age or older.
  • Have at least 6 months of experience in strength training with intensities greater than 75% of one maximum repetition (1-RM).
  • Be classified as active according to the International Physical Activity Questionnaire (IPAQ) score.

You may not qualify if:

  • Musculoskeletal injury within the 6 months prior to the first visit to the laboratory.
  • Recent major surgery (\<3 months).
  • Having a medical condition in which physical activity is contraindicated (assessed with the Physical Activity Readiness Questionnaire, PAR-Q+).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Miguel de Cervantes European University

Valladolid, Valladolid, 47012, Spain

RECRUITING

MeSH Terms

Interventions

High-Intensity Interval TrainingRunning

Intervention Hierarchy (Ancestors)

Physical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological PhenomenaLocomotion

Central Study Contacts

Susana López Ortiz, PhD

CONTACT

Susana López Ortiz, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Masking Details
The researcher responsible for analyzing the data will be blinded to the study conditions.
Purpose
OTHER
Intervention Model
CROSSOVER
Model Details: Quasi-experimental, crossover interventional study
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 9, 2025

First Posted

September 18, 2025

Study Start

October 12, 2025

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

January 31, 2027

Last Updated

March 10, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations