NCT05412511

Brief Summary

In this study, the investigators will be able to estimate the metabolic cost of several foundational medicine ball training exercises.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2022

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

June 1, 2022

Completed
8 days until next milestone

First Posted

Study publicly available on registry

June 9, 2022

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 23, 2023

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2023

Completed
Last Updated

May 11, 2023

Status Verified

May 1, 2023

Enrollment Period

9 months

First QC Date

June 1, 2022

Last Update Submit

May 9, 2023

Conditions

Keywords

functional fitness trainingMedicine ball TrainingEnergy ExpenditureOxygen ConsumptionResistance Trianing

Outcome Measures

Primary Outcomes (5)

  • Change in exercise-induced energy expenditure

    Exercise energy expenditure (kcal) will be measured using a portable indirect calorimetry system

    At pre-exercise, during, and 30 minutes after the exercise session (a single bout lasting 30 seconds)

  • Change in excess post-exercise oxygen consumption (EPOC)

    EPOC (kcal) will be measured using a portable indirect calorimetry system

    At 1 hour after exercise session (single bout lasting 30 seconds)

  • Change in blood lactate concentration (BLa)

    BLa (mmol/L) concentration will be measured in a microphotometer with commercially available kits.

    At pre-exercise and 3 minutes after exercise session (a single bout lasting 30 seconds)

  • Change in heart rate

    Heart rate (bpm) will be measured with a wearable heart rate monitor

    At pre-exercise, during, and 30 minutes after ther exercise session (a single bout lasting 30 seconds)

  • Change in perceived exertion

    Rating of perceived exertion (RPE) will be measured with the Borg scale (0-10)

    At pre-exercise, during, and 30 minutes after the exercise session (a single bout lasting 30 seconds)

Secondary Outcomes (14)

  • Body weight

    At baseline

  • Body height

    At baseline

  • Body mass index (BMI)

    At baseline

  • Waist circumference (WC)

    At baseline

  • Hip circumference (HC)

    At baseline

  • +9 more secondary outcomes

Study Arms (2)

Training

EXPERIMENTAL

Participants in this arm will perform seven medicine ball training exercises (acute bout per exercise) at two different conditions \[Throwing a ball (TB) and no Throwing a ball (NTB)\].

Behavioral: MB-TBBehavioral: MB-NTB

Control

NO INTERVENTION

Participants in this arm will receive no intervention.

Interventions

MB-TBBEHAVIORAL

Training exercises with throwing a medicine ball will be performed for 30 seconds and the training volume will be consisted of 1 repetition.

Training
MB-NTBBEHAVIORAL

Training exercises without throwing a medicine ball will be performed for 30 seconds and the training volume will be consisted of 1 repetition.

Training

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

  • Musculoskeletal injuries
  • Chronic diseases
  • Use of alcohol, caffeine and any type of ergogenic supplements or medication before (≤6 months) and throughout the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Laboratory of Exercise Physiology, Exercise Biochemistry and Sports Nutrition, School of Physical Education, Sports Sciences and Dietetics, University of Thessaly

Trikala, 42100, Greece

Location

Study Officials

  • Ioannis G Fatouros, Prof

    University of Thessaly

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
OTHER
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

June 1, 2022

First Posted

June 9, 2022

Study Start

May 1, 2022

Primary Completion

January 23, 2023

Study Completion

April 30, 2023

Last Updated

May 11, 2023

Record last verified: 2023-05

Locations