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Static Stretching Reshapes Post-RT Recovery

Hemodynamic Load and Local Recovery Patterns After Resistance Training With and Without Static Stretching

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07649785
Enrollment
28
Registered
2026-06-16
Start date
2026-01-12
Completion date
2026-03-10
Last updated
2026-06-16

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

Conditions

Cardiovascular Adaption, Healthy, Healthy Subjects (HS), Recovery Outcomes, Stretching

Keywords

stretching, static stretching, recovery, resistance training, oxygenation

Brief summary

This experimental study investigates the acute cardiovascular and local recovery 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 rate-pressure product and local muscle oxygen saturation, while secondary outcomes include heart rate, blood pressure, brachial artery diameter, tissue hardness, and pressure pain threshold. These measures are used to characterize the short-term effects of the different experimental conditions on systemic hemodynamic load, vascular response, local muscle oxygenation, mechanical tissue status, and pressure pain sensitivity during early recovery.

Interventions

OTHERResistance Training

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 100% of the individual's 8-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 and does not include any additional static stretching beyond the standardized warm-up.

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 100% of the individual's 8-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 flexor), 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 30-35 minutes.

Sponsors

University of Palermo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy male participants ≥ 18 years old

Exclusion criteria

* orthopedic disorders * neurological disorders * metabolic disorders * cardovascular disorders

Design outcomes

Primary

MeasureTime frameDescription
Rate-Pressure Product (RPP)3 times (Baseline, immediately after intervantion and 30 minutes after intervention) for each condition (CC, RT, RT+ST)Rate-pressure product (RPP) will be used as an index of myocardial workload and hemodynamic load during early post-exercise recovery. RPP will be calculated as heart rate multiplied by systolic blood pressure (Omron MX3 Plus). Heart rate and systolic blood pressure will be measured under standardized resting conditions at each time point.
Local Muscle Oxygen Saturation (SmO₂)Time Frame: 3 times (Baseline, immediately after intervantion and 30 minutes after intervention) for each condition (CC, RT, RT+ST)Local muscle oxygen saturation (SmO₂) will be assessed using near-infrared spectroscopy (Moxy Monitor). The sensor will be positioned over the target muscle region and secured to minimize movement artifacts. SmO₂ will be recorded as a local index of the balance between oxygen delivery and oxygen utilization within the sampled muscle region.

Secondary

MeasureTime frameDescription
Brachial Artery diameterTime Frame: 3 times (Baseline, immediately after intervention, and 30 minutes after intervention) for each condition (CC, RT, RT+SS)Brachial artery diameter will be assessed using high-resolution B-mode ultrasound (Esaote MyLab X1 GO, linear-array transducer). The brachial artery will be imaged under standardized conditions, and arterial diameter will be measured at each time point to assess acute changes in conduit artery size during early post-exercise recovery.
Tissue Hardness (TH)Time Frame: 3 times (Baseline, immediately after intervention, and 30 minutes after intervention) for each condition (CC, RT, RT+SS)Tissue hardness (TH) will be assessed using a tissue hardness meter/force gauge (Neutone) at selected muscle sites involved in the exercise protocol, including the pectoral and biceps regions. Measurements will be performed under standardized participant positioning and probe placement conditions. TH will be used as a local mechanical marker of the post-exercise tissue response.
Pain pressure Threshold(PPT)Time Frame: 3 times (Baseline, immediately after intervention, and 30 minutes after intervention) for each condition (CC, RT, RT+SS)Pressure pain threshold (PPT) will be assessed using a pressure algometer(WAGNER, FPX) at selected muscle sites involved in the exercise protocol. The algometer will be applied perpendicular to the skin surface with gradually increasing pressure until the participant reports the first sensation of pain. PPT will be used as a sensory marker of local pressure pain sensitivity during early recovery.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 17, 2026