NCT07618455

Brief Summary

This randomized controlled trial aimed to investigate the effects of a 12-week Whole-Body High-Intensity Interval Training (WB-HIIT) program compared with Moderate-Intensity Continuous Training (MICT) on immune function in recreationally active young adults. Participants were randomly assigned to either WB-HIIT or MICT groups. Immune-related biomarkers and performance outcomes were assessed before and after the intervention. The study sought to determine whether different exercise modalities produce distinct adaptations in immune function.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2020

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 30, 2020

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2020

Completed
5.7 years until next milestone

First Submitted

Initial submission to the registry

May 16, 2026

Completed
16 days until next milestone

First Posted

Study publicly available on registry

June 1, 2026

Completed
Last Updated

June 1, 2026

Status Verified

May 1, 2026

Enrollment Period

2 months

First QC Date

May 16, 2026

Last Update Submit

May 23, 2026

Conditions

Keywords

High-intensity interval trainingmoderate-intensity continuous exerciseimmune systemACTHcortisolexercise immunologyIL-6

Outcome Measures

Primary Outcomes (1)

  • Peripheral immune cell counts

    Changes in peripheral blood leukocyte, lymphocyte subsets, neutrophil, and monocyte counts from baseline to post-intervention (8 weeks).

    Baseline and 8 weeks (post-intervention)

Secondary Outcomes (4)

  • Inflammatory cytokine levels

    Baseline and 8 weeks (post-intervention)

  • Immunoglobulin levels

    Baseline and 8 weeks (post-intervention)

  • Cortisol levels

    Baseline and 8 weeks (post-intervention)

  • Maximal oxygen uptake (VO₂max)

    Baseline and 8 weeks (post-intervention)

Study Arms (2)

Whole-Body HIIT

EXPERIMENTAL

Participants will perform Whole-Body High-Intensity Interval Training (WB-HIIT) protocol.

Behavioral: Whole-Body High-Intensity Interval Training (WB-HIIT)

MICT

ACTIVE COMPARATOR

Participants will perform Moderate-Intensity Continuous Training (MICT) protocol.

Behavioral: Moderate-Intensity Continuous Training (MICT)

Interventions

Whole-body high-intensity interval training protocol performed under supervision.

Whole-Body HIIT

Moderate-intensity continuous training protocol performed under supervision.

MICT

Eligibility Criteria

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

You may qualify if:

  • Healthy male adults Aged 18-25 years Not engaged in regular structured exercise training (\>3 sessions/week) VO₂max within normal healthy range Willingness to participate and provide informed consent No acute or chronic inflammatory, metabolic, or cardiovascular disease

You may not qualify if:

  • Female participants (not included in study design) Smoking or alcohol abuse Use of anti-inflammatory or immunomodulatory drugs Participation in regular high-intensity training programs Musculoskeletal limitations preventing exercise testing or training Acute infection within last 2 weeks Chronic metabolic, cardiovascular, or autoimmune diseases

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bitlis Eren University

Bitlis, Merkez, 13100, Turkey (Türkiye)

Location

Study Officials

  • Melih Çalışır, PhD

    Bitlis Eren Üniversitesi University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
No masking was applied due to the nature of exercise interventions.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants will be randomly assigned to either Whole-Body High-Intensity Interval Training (WB-HIIT) or Moderate-Intensity Continuous Training (MICT) groups.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctoral Researcher

Study Record Dates

First Submitted

May 16, 2026

First Posted

June 1, 2026

Study Start

June 30, 2020

Primary Completion

August 30, 2020

Study Completion

August 30, 2020

Last Updated

June 1, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared due to participant privacy and confidentiality concerns.

Locations