NCT07364149

Brief Summary

This experimental study investigates the acute cardiovascular and vascular responses to a single session of resistance training, with and without additional static stretching, compared with a resting control condition. Participants are allocated to one of three groups (control, resistance training, resistance training plus static stretching) and assessed at baseline, immediately after the session, and 30 minutes post-exercise. Primary outcomes include blood pressure and other hemodynamic or functional measures, in order to explore the short-term impact of these exercise modalities on cardiovascular regulation.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
27

participants targeted

Target at P25-P50 for not_applicable healthy

Timeline
Completed

Started Dec 2025

Shorter than P25 for not_applicable healthy

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 15, 2025

Completed
9 days until next milestone

First Submitted

Initial submission to the registry

December 24, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

January 23, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 10, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 10, 2026

Completed
Last Updated

April 28, 2026

Status Verified

April 1, 2026

Enrollment Period

3 months

First QC Date

December 24, 2025

Last Update Submit

April 26, 2026

Conditions

Keywords

stretchingstatic stretchingResistance trainingResistance exercisetissue stiffnessblood pressureFlow Mediated Dilationheart rate variabilityOxygenation

Outcome Measures

Primary Outcomes (1)

  • Flow Mediated Dilation(FMD%)

    Brachial artery flow-mediated dilation (FMD) will be assessed using high-resolution B-mode ultrasound (Esaote MyLab X1 GO, linear transducer) during a standardized forearm cuff occlusion protocol. Baseline diameter will be recorded for 60 seconds prior to cuff deflation. Reactive hyperemia will be induced by 5-minutes arterial occlusion followed by cuff release, with continuous diameter recording for 3 minutes post-deflation to identify peak diameter.

    3 times (Baseline, immediately after intervantion and 30 minutes after intervention) for each condition (CC, RT, RT+ST)

Study Arms (3)

RT

EXPERIMENTAL

Resistance Training

Other: Resistance Training

RT+SS

EXPERIMENTAL

Resistance training + Static stretching

Other: Resistance training + Static Stretching

CC

NO INTERVENTION

Control Condition --\> participants sat silently on a chair without performing any train

Interventions

Participants assigned to this group will complete a single supervised upper body resistance training session. The protocol includes bench presses and bicep curls performed at 80% of the individual's 1-rep max, for 4 sets of 8 reps, with standardized rest intervals between sets of 2 minutes. The total duration of the session is approximately 20-30 minutes and does not include any additional static stretching beyond the standardized warm-up.

RT

Participants assigned to this group will complete a single supervised upper body resistance training session. The protocol includes bench presses and bicep curls performed at 80% of the individual's 1-rep max, for 4 sets of 8 reps, with standardized rest intervals between sets of 2 minutes. The total duration of the session is approximately 20-25 minutes .Immediately after the resistance exercises, they will complete a structured static stretching protocol targeting the trained muscle groups (pectoralis and elbow flexors), with each stretch held for about 30 seconds and repeated for several sets. The additional stretching lasts 12 minutes, for a total session duration of about 35-40 minutes.

RT+SS

Eligibility Criteria

Age18 Years - 55 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • healthy male participants ≥ 18 years old

You may not qualify if:

  • orthopedic disorders
  • neurological disorders
  • metabolic disorders
  • cardovascular disorders

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Palermo

Palermo, 90144, Italy

Location

MeSH Terms

Interventions

Resistance TrainingMuscle Stretching Exercises

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesPhysical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Ewan Thomas, Associate Professor in Psychology, Educational Science and Human Movement

Study Record Dates

First Submitted

December 24, 2025

First Posted

January 23, 2026

Study Start

December 15, 2025

Primary Completion

March 10, 2026

Study Completion

March 10, 2026

Last Updated

April 28, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations