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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04476615
Other study ID # 140166
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 4, 2017
Est. completion date January 16, 2020

Study information

Verified date July 2020
Source Universita di Verona
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to test a Fasting Mimicking Diet (FMD) for its efficacy on improving muscular resistance and endurance. The investigators will perform a randomized clinical trial to test the efficacy of the FMD on improving muscular strength, muscular resistance and endurance in physically active young adults (18-40 years of age). The study will include two arms: Placebo (Placebo diet) and FMD (3 cycles of 5-day fasting-mimicking diet within two months). Study endpoints will include muscular strength evaluation of lower limbs, cardio-pulmonary responses, neuromuscular function and muscle architecture. Subjects will be evaluated 4 times within 3 months: at baseline (T1), after the 1st cycle of diet (T2), 7 to 15 days after the 3rd cycle of diet maintaining baseline intensity (T3) and with re-assessment of Peak Power Output (T4).


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date January 16, 2020
Est. primary completion date January 16, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Male sex;

- Age Range: 18-40 years old;

- Body Mass Index (BMI) range between 18.5 and 30;

- METs minutes per week - calculated by International physical activity questionnaire (IPAQ) - between 600 and 3000.

Exclusion Criteria:

- Female sex;

- History of muscle, joints and nerves injuries to the upper and/or lower limbs in the previous 12 months;

- Body Mass Index (BMI) below 18.5 and above 30;

- METs minutes per week - calculated by International physical activity questionnaire (IPAQ) - below 600 or above 3000.

Study Design


Intervention

Dietary Supplement:
Fasting-Mimicking Diet (ProLon®)
Dietary restriction: Fasting-Mimicking Diet (ProLon®). 5-days cycles spaced at 1-month intervals for 3 months (3 cycles in total).
Placebo bars
Dietary supplementation: Low-energy bars (L-Nutra®) to integrate the daily nutritional habits - one bar per day. 5-days cycles spaced at 1-month intervals for 3 months (3 cycles in total).

Locations

Country Name City State
Italy Department of Neurosciences, Biomedicine and Movement Sciences Verona

Sponsors (2)

Lead Sponsor Collaborator
Universita di Verona University of Southern California

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference in time to exhaustion (TTE) Difference between time points in time duration [s] of the exercise at a given power output (85%) and cadence (60 RPM), before the given work rate could not be sustained. baseline (T1); day 5 (1°diet cycle - T1), after 2 months (T3 and T4)
Primary Change in maximal voluntary contraction (MVC) Variation between time points in maximal force voluntarily produced by the knee extensor muscles pre- and immediately post exercise, considering for lever length [N*m]. baseline (T1); day 5 (1°diet cycle - T1), after 2 months (T3 and T4)
Primary Change in voluntary (muscle) activation (VA) Change between time points in the percentage of muscle activated by volition. [%] To quantify voluntary activation, the amplitude of the superimposed twitch is expressed as a fraction of the twitch evoked by the same stimulus in the relaxed muscle. baseline (T1); day 5 (1°diet cycle - T1), after 2 months (T3 and T4)
Primary Change in resting twitch force (RT) Force elicited at rest by electrical stimulation of the femoral nerve, considering for lever length [N*m]. baseline (T1); day 5 (1°diet cycle - T1), after 2 months (T3 and T4)
Primary Change in oxygen consumption (VO2) Variations of mean oxygen consumption at rest and at each minute while exercising (performance test). baseline (T1); day 5 (1°diet cycle - T1), after 2 months (T3 and T4)
Primary Change in peak (task-specific) oxygen consumption (VO2) Peak oxygen consumption during the incremental test (maximal value during a 30" time-window). baseline (T1) and after 2 months (T4).
Primary Change in femoral (artery) blood flow (FBF) Measurements of common femoral arterial blood velocity (Vmean) and vessel diameter will be performed using ultrasound Doppler, distal to the inguinal ligament and proximal to the bifurcation of the deep and superficial femoral arteries. (FBF = Vmean p (vessel diameter/2)^2 * 60) at rest and during the performance test. Differences between each time point will be assessed: baseline (T1); day 5 (1°diet cycle - T1), after 2 months (T3 and T4)
Primary Change in median frequency of the power spectrum density of EMG EMG signal from the vastus lateralis (VL) muscle was recorded throughout exercise to estimate the output of spinal motoneurons and the development of peripheral fatigue. during the performance test at each time point: baseline (T1); day 5 (1°diet cycle - T1), after 2 months (T3 and T4)
Secondary Change in carbon dioxide (VCO2) production Variation of physiological production of CO2 at rest and while exercising measured by a breath-by-breath system [L/min]. baseline (T1); day 5 (1°diet cycle - T1), after 2 months (T3 and T4)
Secondary Change in minute ventilation (VE) Difference in ventilatory response at rest and while exercising measured by a breath-by-breath system [L/min]. baseline (T1); day 5 (1°diet cycle - T1), after 2 months (T3 and T4)
Secondary Change in heart rate (HR) Difference in the cardiac response at rest and while exercising measured by a heart rate monitor system. baseline (T1); day 5 (1°diet cycle - T1), after 2 months (T3 and T4)
Secondary Change in Peak Power Output (Wpeak) Difference in maximal power [Watts] achieved (last completed 1-min step) during the incremental test sessions. baseline (T1) and after 2 months (T4).
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