Long-term Adaptations of Skeletal Muscle After Hybrid Training.

NCT ID: NCT07341711

Last Updated: 2026-01-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-01-08

Study Completion Date

2026-12-20

Brief Summary

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Obesity is a major challenge for public health and renders it imperative to reduce its prevalence. High intensity interval training (HIIT) is a form of exercise training that can efficiently induce weight loss in adults with overweight or obesity, even in the absence of dietary intake manipulation. Hybrid type training represents a form of HIIT, that incorporates both cardiorespiratory and musculoskeletal stimuli, by combining multiple types of exercise into a circuit-type, interval style workout. Recent evidence suggests that long-term participation in hybrid HIIT results in significant health-related benefits. However, the molecular mechanisms driving the chronic effects of hybrid HIIT on cardiometabolic and musculoskeletal health remains to be elucidated.

Detailed Description

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A total number of 30 adults (both males and females) aged 30-50, meeting the inclusion criteria, will be enrolled in this study. Participants will be randomly assigned to either (i) a Control group or (ii) an Intervention group. The Intervention group will participate in three hybrid-type HIIT sessions per week over a 6-month period while receiving a balanced diet. The Control group will receive a balanced diet over the 6-month period but will not participate in exercise training. At baseline and 6 months, both groups will undergo assessment of their anthropometric profile, body composition, resting metabolic rate, muscle strength and cardiorespiratory capacity and provide resting blood and skeletal muscle samples.

Conditions

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Obesity & Overweight

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Intervention group

Participants in this arm will participate in three hybrid-type HIIT sessions per week over a 6-month period while receiving a balanced diet

Group Type EXPERIMENTAL

Exercise training

Intervention Type OTHER

Participants will perform a six-month hybrid training program while receiving a balanced diet. The periodization of hybrid training intervention will consist of three 2-month phases of gradually increased exercise intensity and volume. In every training will participate 5-8 individuals. The training will contain 6-12 different exercises (stations), depending on the phase of the intervention, which will be executed in a circuit for a total of 2-3 rounds, with 2-3 minutes of rest period between sets (depending on the phase). The exercise execution will last 20-45 seconds, and the rest between them will last 30-60 seconds (depending on the phase), while the exercise intensity will range from 75 to 85% of maximal heart rate. The stations of hybrid training will contain multi-joint exercises or neuromuscular activation exercises using either body weight resistance or portable equipment.

Control group

Participants in this arm will receive a balanced diet over the 6-month period but will not participate in exercise training

Group Type ACTIVE_COMPARATOR

Control group

Intervention Type OTHER

Participants will receive a balanced diet but will not participate in any type of exercise training over a six month period.

Interventions

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Exercise training

Participants will perform a six-month hybrid training program while receiving a balanced diet. The periodization of hybrid training intervention will consist of three 2-month phases of gradually increased exercise intensity and volume. In every training will participate 5-8 individuals. The training will contain 6-12 different exercises (stations), depending on the phase of the intervention, which will be executed in a circuit for a total of 2-3 rounds, with 2-3 minutes of rest period between sets (depending on the phase). The exercise execution will last 20-45 seconds, and the rest between them will last 30-60 seconds (depending on the phase), while the exercise intensity will range from 75 to 85% of maximal heart rate. The stations of hybrid training will contain multi-joint exercises or neuromuscular activation exercises using either body weight resistance or portable equipment.

Intervention Type OTHER

Control group

Participants will receive a balanced diet but will not participate in any type of exercise training over a six month period.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* BMI: \>25 kg/m2 and \<40 kg/m2
* Untrained individuals (abstain \>1 year from exercise training)
* No dietary intervention over the last 6 months preceding the study
* Low cardiorespiratory fitness level (VO2max: \<45 ml/kg/min)
* No use of any medication, dietary supplements
* Low risk for cardiovascular disease
* A weight loss \<10% over the last 6 months preceding the study
* Fee of non-communicable diseases (excluding metabolic syndrome)

Exclusion Criteria

* Low participation rate (\<80% completion of the exercise training sessions)
* Unbalanced diet
* Participation in additional exercise training regimes
* Cosumption of anti-inflammatory of pain relief medication
Minimum Eligible Age

30 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Thessaly

OTHER

Sponsor Role lead

Responsible Party

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Ioannis G. Fatouros

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Department of Physical Education and Sport Science Trikala, University of Thessaly

Trikala, Thessaly, Greece

Site Status

Countries

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Greece

Central Contacts

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Ioannis G Fatouros, Professor

Role: CONTACT

24310 47047 ext. 0030

Facility Contacts

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Ioannis G Fatouros, Professor

Role: primary

+30 2431047047

Athanasios Z Jamurtas, Professor

Role: backup

+30 2431047054

Other Identifiers

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2482/4.12.2024

Identifier Type: -

Identifier Source: org_study_id

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