- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05482750
Resistance Training in the Fasted State
May 8, 2023 updated by: Eduardo Lusa Cadore, Federal University of Rio Grande do Sul
Effects of Resistance Training Performed in the Fasted State Compared to the Fed State on Morphological and Neuromuscular Adaptations in Young Adults
It is well evidenced in the literature that fasting aerobic exercise generates a series of metabolic differences when compared to exercise performed in the fed state, including the use of fats predominantly as an energy source.
Consequently, increases in adaptations to aerobic training, related to health and physical performance, are observed when sessions are performed in the fasted state.
In relation to resistance training, the evidence is limited.
There is a lack of data in the literature regarding the effects of fasting on resistance exercises and whether this practice may reflect in losses or improvements in morphological and neuromuscular adaptations related to resistance training.
Thus, the aim of the present project is to compare the effects of resistance training performed in the fasted state compared to the fed state during 12 weeks on body composition and physical performance in young adults.
Thirty-four eutrophic or overweight individuals, not engaged in regular resistance exercises, aged between 20 and 40 years, will be recruited.
They will be put on a standard customized diet and will perform 2 weekly sessions of resistance exercise after overnight fasting (10 to 12 hours) or in the fed state, for 12 weeks.
Before, in the middle and after this period, evaluations of body composition, muscle thickness and quality, maximum dynamic strength and maximum power will be analyzed.
Comparisons will be performed using Generalized Estimating Equations (GEE), adopting the factors group (2 stratifications) and time (3 stratifications).
All results will be expressed as mean and standard deviation and the accepted significance level will be 5%.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
28
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Rio Grande Do Sul
-
Porto Alegre, Rio Grande Do Sul, Brazil, 90690-200
- Escola de Educação Física, Fisioterapia e Dança - UFRGS
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Men and women;
- Aged between 19 and 40 years;
- Body mass index (BMI) between 18 and 29.9 kg/m²;
- Not engaged in regular strength physical exercise (>1 weekly session) for the last 3 months.
Exclusion Criteria:
- Smokers;
- Use of medications and/or supplements that may influence the outcomes evaluated;
- Individuals who have a chronic disease that may prevent physical exercise.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Resistance training in the fasted state
Subjects will maintain the standard diet and will perform resistance exercise sessions after overnight fasting (10 to 12 hours).
Over the 12 weeks of intervention, participants will perform two sessions a week of resistance exercises.
|
On the first day of evaluations, the subjects will perform the basal metabolic rate (BMR) analysis, as well as familiarization with the neuromuscular tests.
After the preliminary tests, the volunteers will perform the pre-intervention procedures.
Assessments of body composition, muscle thickness and quality, maximum dynamic strength and maximum power will be performed.
In addition, instruments related to dietary control and physical activity level will be applied.
Subsequently, in a randomized manner, participants will be allocated to one of two different interventions.
During the intervention (8 weeks), the adherence to the standard diet will be verified, as well as body composition, muscle thickness and quality, maximum dynamic strength and maximum power will be reassessed.
After the 12 weeks of intervention, the volunteers will perform the evaluations referring to the post-intervention moment, following the same steps of the pre-intervention collections.
Other Names:
|
|
Active Comparator: Resistance training in the fed state
Subjects will maintain the standard diet and will perform resistance exercise sessions in the fed state, between 1 and 2 hours after consuming a carbohydrate-containing meal.
Over the 12 weeks of intervention, participants will perform two sessions a week of resistance exercises.
|
On the first day of evaluations, the subjects will perform the basal metabolic rate (BMR) analysis, as well as familiarization with the neuromuscular tests.
After the preliminary tests, the volunteers will perform the pre-intervention procedures.
Assessments of body composition, muscle thickness and quality, maximum dynamic strength and maximum power will be performed.
In addition, instruments related to dietary control and physical activity level will be applied.
Subsequently, in a randomized manner, participants will be allocated to one of two different interventions.
During the intervention (8 weeks), the adherence to the standard diet will be verified, as well as body composition, muscle thickness and quality, maximum dynamic strength and maximum power will be reassessed.
After the 12 weeks of intervention, the volunteers will perform the evaluations referring to the post-intervention moment, following the same steps of the pre-intervention collections.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body mass
Time Frame: 1 minute
|
Body mass will be measured using a scale (Urano, Canoas, Brazil).
|
1 minute
|
|
Lean body mass
Time Frame: 15 minutes
|
Lean body mass will be determined using the dual energy X-ray absorption (DEXA) method, using a densitometry machine (Hologic GE, Bedford, USA).
|
15 minutes
|
|
Fat body mass
Time Frame: 15 minutes
|
Fat body mass will be determined using the dual energy X-ray absorption (DEXA) method, using a densitometry machine (Hologic GE, Bedford, USA).
|
15 minutes
|
|
Muscle thickness
Time Frame: 30 minutes
|
Muscle thickness will be evaluated through ultrasound (Nemio XG, Toshiba, Japan).
|
30 minutes
|
|
Muscle quality
Time Frame: 30 minutes
|
Muscle quality will be evaluated through echo intensity of the quadriceps through ultrasound (Nemio XG, Toshiba, Japan).
|
30 minutes
|
|
Maximum dynamic strength
Time Frame: 30 minutes
|
Maximum dynamic strength will be assessed using the 1 repetition maximum (1RM) test for bench press and knee extension exercises.
|
30 minutes
|
|
Maximum power
Time Frame: 30 minutes
|
The maximum power and the medium power will be evaluated in the bench press and knee extension exercises considering a load of 30 and 70% of 1RM.
|
30 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 23, 2022
Primary Completion (Actual)
December 23, 2022
Study Completion (Actual)
December 23, 2022
Study Registration Dates
First Submitted
July 25, 2022
First Submitted That Met QC Criteria
July 28, 2022
First Posted (Actual)
August 1, 2022
Study Record Updates
Last Update Posted (Actual)
May 9, 2023
Last Update Submitted That Met QC Criteria
May 8, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- URioGrandeESEFID
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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