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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03662152
Other study ID # CEI UCJC
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 7, 2018
Est. completion date June 30, 2018

Study information

Verified date September 2018
Source Centro Universitario La Salle
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose: To compare the effects between non-vibration foam rolling (NVFR) and vibration foam rolling (VFR) on visual analogic scale (VAS), pressure pain threshold (PPT), oxygen saturation (SmO2), counter-movement jump (CMJ), and hip and knee range of movement (ROM) after induction of muscle damage through eccentric acute-exercise using inertial flywheel.

Methods: Thirty-eight healthy subjects (males n=32 females= 6, age 22.2±3.2 years) were randomly assigned in a counter-balanced fashion to either a VFR or NVFR protocol group. All subjects performed a 10x10 (sets x reps) eccentric squat protocol to induce muscle damage. The protocols were administered 48-h post-exercise, measuring VAS, PPT, SmO2, CMJ and ROM, before and immediately post-treatment. The technique of treatment was repeated on both legs for 1 min for a total of 5 sets, with a 30-s rest between sets.


Description:

Muscle damage was induced with overload eccentric training using inertial flywheel (2.7-kg flywheels with a moment inertia of 0.07 kg m−2). Immediately after baseline measures, subjects performed 10 sets x 10 repetitions parallel squats using a gravity-free training device flywheel with 2 minutes of recovery between sets. The squat exercise was chosen as basic movement because of its similar muscles recruitment to many athletic movements patterns. Furthermore, the squat exercise is one of the main exercises used to improve the lower-body strength. The required technique was demonstrated to all subjects before beginning the eccentric session, and they were coached during the protocol to be sure adequate technique and maximal effort in each repetition were maintained. All participants performed 5 min on a treadmill to warm up before performing the eccentric bout.

Description of the foam roller intervention The foam-rolling technique was based on a previously published protocol. In both protocols, the technique was repeated on both legs for 1 min for a total of 5 sets, with a 30-s rest between sets. The cadence for both techniques (NVFR and VFR) was fixed at 3:4 using a metronome.

Using a protocol adapted from previous study, subjects began in the plank position with the foam roller at the most proximal portion of the quadriceps of both legs, with as much of their body mass as possible on the foam roller.

Non-Vibration Foam Rolling (NVFR) Group: subjects performed the FR protocol using a custom-made foam roller composed of a polystyrene foam cylinder (15-cm diameter × 35-cm long).

Vibration Foam Rolling (VFR) Group: subjects performed the same protocol using a foam roller with vibration (frequency: 18 Hz) composed of a polystyrene foam cylinder (15-cm diameter × 35-cm long).


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date June 30, 2018
Est. primary completion date May 11, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- All subjects were free from musculoskeletal disorders in the last year. All subjects were asked to abstain from unaccustomed exercise, all medications and dietary supplements 72 hours before baseline measurements, during the experimental period and post-treatment

Exclusion Criteria:

- Subjects with symptoms or pathology,

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Foam roller
Foam roller massage after DOMS
Vibration foam roller
Foam roller massage with vibration after DOMS

Locations

Country Name City State
Spain Centro Superior de Estudios Universitarios La Salle Madrid

Sponsors (2)

Lead Sponsor Collaborator
Daniel Muñoz-Garcia Camilo Jose Cela University

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary visual-analogue scale (VAS) used to measure DOMS and to estimate the intensity of its associated pain. In order to standardize the scaling instructions, the endpoints were described for the subject as 0 = 'no sensation' and 10 = 'the most worst intense sensation imaginable' (16,40). The VAS was measured in four different conditions: 1) passive, 2) during isometric quadriceps contraction, 3) performing a squat and 4) during stretch quadriceps. 2 seconds
Primary Pressure pain threshold measured using a digital pressure algometer (Microfet3 ®, Hoggan Health Industries). The digital dynamometer with a 1 cm probe was used to measure three points at the quadriceps: vastus lateralis (VL), rectus femoris (RF) and vastus medialis (VM). Subject was lying on the stretcher, the algometer was positioned perpendicularly to the skin at each point and gradual pressure was applied until the subject reported a change from the sensation of pressure to pain. In that point the pressure was stopped immediately and the value was recorded represented the pain threshold (16). The mean of the 3 measures was calculated. Algometry has been shown to be highly reliable (ICC = 0.91) (9). 1 minute
Primary Muscle oxygenation was recorded at rest, during 10 squat repetitions (body weight load) and immediately after, using a commercially available portable non-invasive near infrared spectroscopy (NIRS) device (Moxy, Fortiori Design LLC, Minnesota, USA). 2 minutes
Secondary Infrared Optojump photoelectric cells (Microgate Corporation, Bolzano, Italy) were used to measure explosive strength in lower limbs 5 minutes
Secondary Passive and active hip extension and knee flexion ROM of the dominant leg were measured with a Microfet3 ® inclinometer using the protocol of Norkin & White 2 minutes
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