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CompletedNCT07433543Updated Feb 25, 2026

Foam Rolling, Blood Pressure and Range of Motion

An interventional study of Cervical foam rolling in Healthy Participants and Healthy Young Adults, sponsored by University of Palermo. Completed at 1 site in Italy. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-25.

Sponsored by University of Palermo · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled May 2025, registered Feb 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Foam rolling (FR) is a technique involving the application of external pressure to muscles and connective tissues using different devices (e.g. foam rollers, massage rollers, balls, etc.) , with the aim of reducing muscle tension, soreness, and stiffness, and improving circulation, and flexibility. Emerging evidence suggests that FR may also enhance tissue perfusion and blood flow and could induce a relaxation response, potentially modulating autonomic balance toward increased parasympathetic activity. The cervical region is of particular interest due to the presence of clinically relevant vascular structures, such as the carotid arteries, whose mechanical stimulation may elicit cardiovascular responses. Accordingly, the present study was designed to investigate the acute effects of cervical foam rolling on blood pressure, while simultaneously examining tissue hardness and heart rate variability as potential underlying mediators, and to explore a possible dose-response relationship between foam rolling volume and blood pressure through an inter-set analysis. Additionally, the acute effects of cervical foam rolling on local range of movement were also investigated.

02

Conditions studied

  • Healthy Participants
  • Healthy Young Adults

Keywords

  • blood pressure
  • heart rate variability
  • stiffness
  • massage roller
  • range of motion
  • flexibility
  • cervical
03

In context

Lead sponsor

University of Palermo is the lead sponsor of 142 studies on the registry; 28 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • healthy participants aged 18 years or older

Exclusion criteria

Exclusion Criteria:

  • use of antihypertensive medication;
  • orthopedic, neurological, renal, metabolic, or cardiovascular disorders.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Experimental
    Cervical foam rolling

    Four sets of 45 foam rolls were self-administered on the right posterolateral cervical region, with 45 seconds of recovery between sets.

    Other: Cervical foam rolling

  • No intervention
    Control

    Participants in the control condition remained seated for 6 minutes, matching the duration of the FR intervention protocol.

Interventions

  • OtherCervical foam rolling

    FR condition: Four sets of 45 foam rolls were self-administered, by using a massage roller, on the right posterolateral cervical region, with 45 seconds of recovery between sets.

06

What researchers measure

Primary outcomes

  1. Systolic pressure, diastolic pressure, and mean arterial pressure

    Systolic and diastolic BP were measured by using a validated oscillometric device. During the blood pressure assessment, participants were instructed to remain seated and relaxed. The mean arterial pressure (MAP) was subsequently extrapolated using the following formula: MAP=DP+1/3(SP-DP).

    Time frame: - Day 1: Baseline (upon arrival) and immediately post-intervention; - Day 2: Baseline (upon arrival) and immediately post-intervention.

  2. Tissue Hardness

    Tissue hardness was collected using a portable tissue hardness meter. In the cervical region, the spinous process of C7 was used as the reference point. Measurements were obtained bilaterally to the C7.

    Time frame: - Day 1: Baseline (upon arrival) and immediately post-intervention; - Day 2: Baseline (upon arrival) and immediately post-intervention.

  3. Heart rate variability

    Heart rate variabity was collected using a Polar H10 sensor chest strap device, a device validated for assessment of RR intervals.

    Time frame: - Day 1: Baseline (upon arrival) and immediately post-intervention; - Day 2: Baseline (upon arrival) and immediately post-intervention.

  4. Cervical range of motion (ROM)

    Cervical ROM was measured using an inertial measurement unit (GYKO; Microgate, Bolzano, Italy). The accelerometer was secured to the participant's forehead and measured active cervical flexion, extension, right and left rotation, and right and left inclination.

    Time frame: - Day 1: Baseline (upon arrival) and immediately post-intervention; - Day 2: Baseline (upon arrival) and immediately post-intervention.

07

Study locations

1 site
  • University of Palermo
    Palermo, Italy
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 25, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07433543
Lead sponsor
University of Palermo
Responsible party
Ewan Thomas (Ewan Thomas - Associate Professor, Department of Psychology, Educational Science, and Human Movement, University of Palermo) — Principal investigator
First posted
Feb 25, 2026
Start date
May 26, 2025
Primary completion
Jul 30, 2025
Completion
Jul 31, 2025
Last update
Feb 25, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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