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Hybrid Exercise Training for Weight Loss

Not Applicable
Completed
Conditions
Circuit-based High Intensity Interval Training
Habitual Physical Activity
Performance
Body Composition
Resting Metabolic Rate
Interventions
Behavioral: DoIT workout
Behavioral: DoIT workout - Detraining
Behavioral: Control - No training
Registration Number
NCT03134781
Lead Sponsor
University of Thessaly
Brief Summary

In this study the investigators utilized a novel hybrid HIIT (high intensity interval training) exercise training approach, the Hybrid Interval Training (DoIT) workout that combines interval training, resistance exercise training and functional training in order to test the hypothesis that DoIT will be able to: i) reduce body mass, ii) improve body composition and iii) alter energy balance, of previously inactive, overweight/obese women.

Detailed Description

In a controlled randomized, two-group, repeated measures design, 65 healthy, sedentary, premenopausal overweight or obese women were randomly assigned to one of three groups: (a) a control group (C, N=21) that participated only in measurements, (b) a training group (TR, N=14) that participated in a supervised 40-week DoIT workout exercise training program and (c) a training-detraining group (TRD, N=14). During the first 20 weeks, TR and TRD followed exactly the same training protocol. At the end of this period, TR continued training for 20 more weeks whereas TRD terminated training for 20 weeks (detraining). Anthropometric, metabolic, daily nutritional intake, habitual physical activity and performance measurements were performed in all groups at baseline, at 20 weeks and 40 weeks.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
49
Inclusion Criteria
  • (a) were sedentary (<7,500 steps/day; VO2max <30 ml/kg/min), b) premenopausal women aged 30-45 years, c) were overweight or obese class 1 (BMI=25-34.9 kg/m2), d) were non-smokers for ≥6 months before the study, e) not following a diet intervention or using nutritional supplements/medications before (≥6 months) and during the study, f) had no weight loss greater >10% of body mass ≤6 months before the study, g) participated in ≥80% of total exercise sessions, and h) had no symptoms of depression.
Exclusion Criteria
  • a) a recent febrile illness, b) history of muscle lesion, c) lower limb trauma, d) signs, symptoms or diagnosis of serious health complications or physical disability or other medical condition compromising safe participation in exercise training.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
TrainingDoIT workoutParticipated in a supervised 40-week DoIT workout exercise training program and in measurements at baseline, at 20 weeks and at 40 weeks.
Training-DetrainingDoIT workout - DetrainingParticipated in a supervised 20-week DoIT workout exercise training program and then entered a 20-week detraining period. They also participated in measurements at baseline, at 20 weeks and at 40 weeks.
ControlControl - No trainingParticipated only in measurements at baseline, at 20 weeks and at 40 weeks.
Primary Outcome Measures
NameTimeMethod
Change in body massAt baseline, at 20 weeks and at 40 weeks.
Change in fat massAt baseline, at 20 weeks and at 40 weeks.

Fat mass assessed by whole-body dual-energy X-ray absorptiometry (DXA).

Change in resting metabolic rateAt baseline, at 20 weeks and at 40 weeks.

Measured using a portable open-circuit indirect calorimeter with a ventilated hood system.

Change in body mass indexAt baseline, at 20 weeks and at 40 weeks.
Change in waist circumferenceAt baseline, at 20 weeks and at 40 weeks.
Change in body fat.At baseline, at 20 weeks and at 40 weeks.

Body fat assessed by whole-body dual-energy X-ray absorptiometry (DXA).

Change in hip circumferenceAt baseline, at 20 weeks and at 40 weeks.
Change in waist-to-hip ratioAt baseline, at 20 weeks and at 40 weeks.
Change in fat-free massAt baseline, at 20 weeks and at 40 weeks.

Fat-free mass assessed by whole-body dual-energy X-ray absorptiometry (DXA).

Change in exercise-induced caloric expenditure.At baseline, at 20 weeks and at 40 weeks.

Measured using a portable indirect calorimetry system

Secondary Outcome Measures
NameTimeMethod
Change in blood lactate concentrationPre-exercise, during the exercise and post-exercise at baseline, at 20 weeks and at 40 weeks.
Change in habitual physical activityAt baseline, at 20 weeks and at 40 weeks.

Seven-day habitual physical activity was assessed by accelerometry

Change in dietary intakeAt baseline, at 20 weeks and at 40 weeks.

Assessed using 7-day diet recalls

Change in maximal strength (1RM)At baseline, at 20 weeks and at 40 weeks.

Measured bilaterally on a horizontal leg press.

Change in maximal oxygen consumption (VO2max)At baseline, at 20 weeks and at 40 weeks.

Assessed by a portable open-circuit spirometry system.

Trial Locations

Locations (1)

Exercise Biochemistry Laboratory, School of Physical Education & Sports Sciences, University of Thessaly

🇬🇷

Trikala, Karies, Greece

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