Metabolic Cost of Sandbag Training

December 18, 2023 updated by: Dimitrios Draganidis, University of Thessaly
This study aims at investigating the metabolic cost of several fundamental exercises with sandbag. Sandbag training has become a popular training modality that is efficiently used to improve cardiovascular status and physical performance. Despite its widespread use and popularity the metabolic cost of exercises using sandbag remains to be elucidated. Therefore, the metabolic cost of various fundamental exercise with sandbag will be determined to aid the planning of exercise training programs.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Ten healthy young adults will be assigned to this study. Participants will initially undergo a baseline assessment of their anthropometrics, body composition (by DXA), resting metabolic rate (RMR), cardiorespiratory fitness (VO2max), muscular strength [maximal strength (1RM) and muscular endurance] and functional capacity. After baseline screening, participants will execute in different days (one exercise per day) one set of each of the following 8 exercise: (1) lateral bag drag, (2) dead bag, (3) shoulder to shoulder thruster, (4) sumo DL with pull, (5) front lunge, (6) single leg RDL, (7) reverse lunge with rotation and (8) clean, in two different conditions: (i) 30 sec and (ii) 45 sec exercise duration, in a random order. Prior to each exercise resting heart rate, blood lactate concentration, oxygen consumption and rate of perceived exertion will be recorded. Heart rate and oxygen consumption (through portable gas analyzer) will be continuously monitored during the exercise and after the end of it, until the oxygen consumption reach the pre-exercise values (excess post-exercise oxygen consumption). Blood lactate and rate of perceived exertion will be reassessed post-exercise.

Study Type

Interventional

Enrollment (Actual)

10

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

    • Karyes
      • Trikala, Karyes, Greece, 42100
        • Laboratory of Exercise Physiology, Exercise Biochemistry and Sports Nutrition, Department of Physical Education and Sport Science, University of Thessaly

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Aged between 18 and 35 years
  • Physically active individuals
  • Free of chronic diseases
  • Free of musculoskeletal injuries
  • Nonsmokers

Exclusion Criteria:

  • Chronic disease
  • Musculoskeletal injury
  • Consumption of alcohol, caffeine and any type of ergogenic supplement during the study.

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: Screening
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: 30-SEC
Participants will execute each exercise for 30 seconds
Both arms include an exercise intervention consisted of 8 different exercises with sandbag: (1) lateral bag drag, (2) dead bag, (3) shoulder to shoulder thruster, (4) sumo DL with pull, (5) front lunge, (6) single leg RDL, (7) reverse lunge with rotation and (8) clean
Experimental: 45-SEC
Participants will execute each exercise for 45 seconds
Both arms include an exercise intervention consisted of 8 different exercises with sandbag: (1) lateral bag drag, (2) dead bag, (3) shoulder to shoulder thruster, (4) sumo DL with pull, (5) front lunge, (6) single leg RDL, (7) reverse lunge with rotation and (8) clean

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in exercise energy expenditure
Time Frame: At pre-exercise, during and up to 15 minutes after the exercise (a single set lasting 30 or 45 seconds)
Total energy expenditure (kcals) during the exercise will be assessed by summing the kcals of the oxidative system, the glycolytic system and the excess post-exercise oxygen consumption.
At pre-exercise, during and up to 15 minutes after the exercise (a single set lasting 30 or 45 seconds)
Change in recovery energy expenditure
Time Frame: At pre-exercise and up to 15 minutes after the exercise (a single set lasting 30 or 45 seconds)
The contribution of excess post-exercise oxygen consumption in exercise energy expenditure will be assessed by the change in oxygen consumption after the exercise using a portable gas analyzer
At pre-exercise and up to 15 minutes after the exercise (a single set lasting 30 or 45 seconds)
Change in aerobic energy expenditure
Time Frame: At pre-exercise and during the exercise (a single set lasting 30 or 45 seconds)
The contribution of oxidative system in exercise energy expenditure will be assessed by the change in oxygen consumption during the exercise using a portable gas analyzer
At pre-exercise and during the exercise (a single set lasting 30 or 45 seconds)
Change in anaerobic energy expenditure
Time Frame: At pre-exercise and post-exercise (a single set lasting 30 or 45 seconds)
The glycolytic contribution to exercise energy expenditure will be assessed by the change in blood lactate concentration after the exercise
At pre-exercise and post-exercise (a single set lasting 30 or 45 seconds)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in blood lactate concentration
Time Frame: At pre-exercise and 4 minutes after the exercise session
Blood lactate concentration will be assessed using a portable automatic analyzer
At pre-exercise and 4 minutes after the exercise session
Change in heart rate
Time Frame: At pre-exercise, during and up to 15 minutes after the exercise session.
Heart rate will be assessed using a wearable heart rate monitor
At pre-exercise, during and up to 15 minutes after the exercise session.
Change in respiratory exchange ratio
Time Frame: At pre-exercise, during and up to 15 minutes after the exercise session.
Respiratory exchange ratio will be assessed using a portable gas analyzer.
At pre-exercise, during and up to 15 minutes after the exercise session.
Change in rate of perceived exertion
Time Frame: At pre-exercise and post-exercise session.
Perceived exertion will be assessed using the Borg Rating of Perceived Exertion Scale (0-10), with ''0'' indicating ''No Exertion'' and ''10'' indicating ''Maximal Exertion''.
At pre-exercise and post-exercise session.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Dimitrios Draganidis, PhD, University of Thessaly

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)

October 15, 2023

Primary Completion (Actual)

November 30, 2023

Study Completion (Actual)

December 15, 2023

Study Registration Dates

First Submitted

October 6, 2023

First Submitted That Met QC Criteria

October 6, 2023

First Posted (Actual)

October 12, 2023

Study Record Updates

Last Update Posted (Estimated)

December 19, 2023

Last Update Submitted That Met QC Criteria

December 18, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

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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