Obesity Clinical Trial
Official title:
Interactive Effects of an Isocaloric High-protein Diet and Resistance Exercise on Body Composition, Ghrelin, and Metabolic and Hormonal Parameters in Untrained Overweight Young Men
Background: The interactive effects of resistance training and dietary protein on hormonal
responses in overweight or obese adults are not clear and remain controversial.
Investigators tested the effect of an isocaloric high-protein diet on body composition,
ghrelin, and metabolic and hormonal parameters during a 12-week resistance training program
in untrained overweight healthy young men.
Methodology: Investigators randomized 18 healthy young males to a standard diet (ST group)
or an isocaloric high protein diet (HP group). Subjects in both groups participated in a 12
week-resistance exercise program. Investigators measured body composition, lipid profile,
homeostatic model assessment of insulin resistance (HOMA-IR) indices, total ghrelin, and
exercise related hormones at baseline and 12 weeks.
Background: The interactive effects of resistance training and dietary protein on hormonal
responses in overweight or obese adults are not clear and remain controversial.
Investigators tested the effect of an isocaloric high-protein diet on body composition,
ghrelin, and metabolic and hormonal parameters during a 12-week resistance training program
in untrained overweight healthy young men.
Methodology: Investigators randomized 18 healthy young males to a standard diet (ST group)
or an isocaloric high protein diet (HP group). They have not participated in any
weight-management program during the previous 6 months. An open-label design will be used.
At enrolment, participants will randomly assign to one of two groups: a control group with a
standard diet (total calories 2,400 kcal/day, 60% carbohydrate, 15% protein and 25% fat; ST
group) and an interventional group with an isocaloric high protein diet (total calories
2,400 kcal/day, 55% carbohydrate, 30% protein and 15% fat; HP group). Participants in both
groups take part in a scheduled resistance exercise training program. Participants does not
take part in any other resistance training program or competitive sport over the study
duration. At the start of the study, participants will be instructed to maintain their
assigned diet throughout the study period. This will be assessed using a food frequency
questionnaire (FFQ) with a 24-h recall after 12 weeks. Participants are presented with
two-dimensional food pictures of the actual size of portions on a computer by a single
trained dietitian to minimize interviewer bias. Medium are defined as the portion sizes
shown, small are approximately half the medium portion size, and large are one-and-a-half
times the medium portion size.
Exercise Protocol All participants will be under supervision during participation in the
progressive supervised resistance exercise-training program. They participate in an onsite
supervised protocol for 12 weeks (6 days per week). Exercise duration will be increased
gradually, from 50 min at week 1 to 80 min at week 12, including warm-up for 20 min and
cool-down periods for 10 min by carrying out gentle stretching exercises of the upper and
lower limbs. A one repetition maximum (1-RM) is the maximum weight that can be lifted for
one complete repetition of the movement. For each participant, the RM will be calculated for
a particular muscle group. Each movement will be carried out at 60-80% of his 1-RM.
Resistance will be increased slowly by three steps; step 1 (60-70% of his 1-RM for week
1-4), step 2 (65-75% of his 1-RM for week 5-8) and step 3 (70-80% of his 1-RM for week
9-12).
Baseline and Follow-up Measurements Height and bodyweight are measured using a digital scale
with the examinee wearing a light gown, but no shoes. Body mass index (BMI) are calculated
as weight (kg) divided by height squared (m2). The percentage body fat and total fat mass
are measured by bioelectric impedance analysis (Inbody 3.0; Biospace Co., Ltd., Seoul,
Korea), a sensitive test for quantification of changes in lean and fat mass in vivo and for
assessment of regional fat distribution. A mercury sphygmomanometer are used for measurement
of blood pressure (BP) of each participant, in the sitting position, after a 10-min resting
period. Two readings each for the systolic and diastolic Bps are recorded at 3-min
intervals, and the average of each measurement are included in our analysis.
Blood samples are obtained preprandially at 0.800 hours from each participant's antecubital
vein after a 12-h fast, and are used for determination of plasma glucose, insulin, lipid
profile, total ghrelin, GH, insulin-like growth factor-1 (IGF-1), testosterone and cortisol.
Blood samples are obtained at baseline (prerandomization) and 12 weeks after randomization.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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