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The Effects of Inter-set Stretching on Muscle Performance

The Effects of Inter-set Stretching on Muscle Performance

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06791733
Enrollment
40
Registered
2025-01-24
Start date
2024-11-02
Completion date
2025-07-31
Last updated
2025-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Brief summary

Static passive muscle stretching, performed weekly, can increase muscle flexibility and range of motion. Typically, static stretching is performed either before starting specific exercises or at the end of a workout. However, the effects of static passive stretching when performed during sets are still not entirely clear in terms of performance. This study aims to evaluate the effects of inter-set stretching on muscle performance

Detailed description

This project aims to evaluate the potential effects of stretching exercises on muscular performance. In particular, we aim to administer passive static stretching between sets of a bench press performance. Within this project we will carry out a crossover design project in which the participants will be tested for two conditions and one control session. The main protocol consists of performing five sets of bench press at 70% of 1-RM. The 1-RM will be calculated before the start of the data collection procedure, through a standardized and validated approach. The experimental sessions will comprise two interventions. The first intervention will be to administer the stretching protocol to the agonist muscles involved in the bench press performance (pectoralis muscles). While the second intervention will be to administer the stretching protocol to the antagonist muscles involved in the bench press performance (dorsal muscles). Within the control session the participants will not perform any stretching between sets. The three arms will be randomized. As outcome variables, the primary outcome will be the comparison of the total volume across each agonist, antagonist, and control session. The secondary outcomes to be assessed are strength, power, velocity, and volume.

Interventions

OTHERPassive static stretching

the intervention consists of passive static stretching of agonist or antagonist muscles between sets

Sponsors

University of Palermo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Healthy men aged ≥ 18 years. * At least 6-month experience of resistance training. * No previous musculoskeletal injuries in the 6 months prior to the study will be recruited

Exclusion criteria

* Participants who suffered an injury within the 6 months prior to the study and/or participants with pathological conditions affecting the musculoskeletal system will not be recruited. * Female participants * Participants with less than 18 years. * Participants who match all inclusion criteria but who fail to attend one or more of the agonist/antagonist stretching sessions will be also excluded.

Design outcomes

Primary

MeasureTime frameDescription
Muscular performanceFrom enrollment to the end of a treatment at 2 weeksThe total volume across each agonist, antagonist, and control session

Secondary

MeasureTime frameDescription
StrengthFrom enrollment to the end of a treatment at 2 weeksStrength, measured in Newtons, will be evaluated using the 'T-Force' device, which records and collects the main biomechanical parameters, including strength, during the concentric and eccentric phases of movement.
PowerFrom enrollment to the end of a treatment at 2 weeksPower, measured in Watts, will be evaluated using the 'T-Force' device, which records and collects the main biomechanical parameters, including power, during the concentric and eccentric phases of movement.
VelocityFrom enrollment to the end of a treatment at 2 weeksVelocity, measured in meters per second, will be evaluated using the 'T-Force' device, which records and collects the main biomechanical parameters, including velocity, during the concentric and eccentric phases of movement.

Countries

Italy

Contacts

Primary ContactLuca Di Bartolo
luca.dibartolo01@unipa.it+393206435580

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026