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CompletedNCT04161300FRvsMTAthUpdated Mar 2, 2021

Foam Rolling and Orthopaedic Manual Physical Therapy in Athletes

An interventional study of Foam Rolling (FR) and Control Group (CG) in Athletic Injuries, sponsored by University of Valencia. Completed at 1 site in Spain. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-03-02.

Sponsored by University of Valencia · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
45
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

The main objective of the present study was to evaluate whether FR massage is effective in improving dynamic balance, flexibility and dynamic strength after intense exercise recovery compared to OMPT protocol or a control group. The present study was a randomized controlled trial. Amateur athletes will be recruited from two athletic clubs. Participants will be randomizing and allocating into three non-balanced groups through a computer software by an external assistant who will be blinding to the study objectives: FR group (n = 18), OMPT group (n = 15) and control group (CG) (n = 14). The intervention period will be lasting one day (1 session). Participant assessment will be perform twice: prior to the study (pre-intervention) and immediately after finishing the intervention (post-intervention).

Interventions: FR group. FR auto-massage will place the foam roller between their ischial tuberosity and a hard surface (i.e., the floor) with their legs held in an extended position, keeping their ankles relaxed and oriented upward. For FR in the lumbar region, participants use their weight to slide the FR through the erector of the lumbar and thoracic spine. The total approximate duration will be about 10-15 minutes; OMPT group. Based on the protocol used by Espí-López et al.: a) Unspecific and bilateral lumbar thrust (L5-S1), one of each side were performed; The total duration will be approximately 10-15 minutes.; CG. The CG did not receive any intervention.

Outcomes will be Lumbar flexibility, Hip flexion, Dynamic balance, Standing Jump and Impression of Change.

Read the detailed description

Introduction Foam rolling (FR) is a form of self-massage in which the targeted musculature is rolled and compressed using a FR. In the field of physical therapy that has been shown to produce a reduced feeling of fatigue in healthy athletes12 as well as hypoalgesic effects in subjects with delayed-onset muscle soreness.

Currently, self-massage through FR is commonly used in the sports field. The reason for this is that it has been suggested that it could have the positive effects traditionally associated with orthopedic manual physical therapy (OMPT), That is why despite the widespread use of FR massage in the field of muscle recovery in athletes, there is a lack of scientific literature about its effectiveness compared to OMPT that can justify its use. Therefore, the main objective of the present study was to evaluate whether FR massage is effective in improving dynamic balance, flexibility and dynamic strength after intense exercise recovery compared to OMPT protocol or a control group.

Methods The present study was a randomized controlled trial. Participants Amateur athletes will be recruited from two athletic clubs. The inclusion criteria will be as follows: (a) male and female amateur athletes aged 18 to 30 years. The exclusion criteria: (a) previous surgery of the locomotor system in lower limbs; (b) musculoskeletal injuries in any part of the body that prevent practicing sports; (c) understanding or communication difficulties; and (d) insufficient fluency in the Spanish language to follow measurement instructions.

Informed written consent will be obtaining from all the participants prior to inclusion. All the participants will be explaining the study procedures, which will be design according to the ethical standards of the Helsinki Declaration.

Procedure Participants will be randomizing and allocating into three non-balanced groups through a computer software by an external assistant who will be blinding to the study objectives: FR group (n = 18), OMPT group (n = 15) and control group (CG) (n = 14). The intervention period will be lasting one day (1 session).

Participant assessment will be perform twice: prior to the study (pre-intervention) and immediately after finishing the intervention (post-intervention).

Interventions FR group. FR auto-massage will place the foam roller between their ischial tuberosity and a hard surface (i.e., the floor) with their legs held in an extended position, keeping their ankles relaxed and oriented upward. For FR in the lumbar region, participants use their weight to slide the FR through the erector of the lumbar and thoracic spine. The total approximate duration will be about 10-15 minutes.

OMPT group. Based on the protocol used by Espí-López et al.: a) Unspecific and bilateral lumbar thrust (L5-S1), one of each side were performed; b) Hip joint decompression, performing 25 repetitions c) Hip rotator stretch with hip and knee flexion, 15 repetitions; d) Femorotibial decompression, 25 reps. e) Quadriceps femoral muscle compression and traction, 25 repetitions; f) Opening of the internal and external femorotibial interline, 15 repetition; g) Ankle decompression, 3 repetitions; h) Posteroanterior and anteroposterior mobilization of head and base of fibula, 25 repetitions. The total duration will be approximately 10-15 minutes.

CG. The CG did not receive any intervention.

Primary outcomes: Physical functional variables Lumbar flexibility. Modified Schober test (MMST). The MMST was designed to assess the mobility of the entire lower back, so the MMST was used to measure lumbar flexion before and after FR and TM interventions. The examiner will place his thumbs on the lower margin of the posterior-upper iliac spine (lower reference point) and a pen mark was made. While the examiner held the tape against the subject's skin, another signal was marked 15 cm above the first (upper reference point). Each subject was then asked to perform an active flexion of the entire trunk and the distance between the two points will be measuring and then the subject return to his initial position. The difference between the initial distance and the new bending measurements will be take.

Hip flexion. by the passive straight leg raise (SLR). Passive SLR will be conducting using a procedure previously described by Hopper et al. A Richards splint and an ankle foot orthosis were applied to the left leg to maintain the knee in full extension and the ankle at a neutral plantar angle. An inclinometer will be attaching to a belt, which will place around the pelvis at the level of the anterior superior iliac spine (Baseline Bubble Inclinometer. Fabrication Enterprises, PO Box, 1500 White Plains, NY 10602, USA). A second inclinometer will be then attaching to the Richards splint at the level of the knee joint line. The mean of 3 measures will be using for analysis. During the test, the participants are positioned with their hands on the abdomen, cervical spine in a neutral position and eyes closed.

Dynamic balance using the Star Excursion Balance Test (SEBT). The SEBT is a dynamic test that requires strength, flexibility, and proprioception. The goal of the SEBT is to maintain single-leg stance while reaching as far as possible with the contralateral leg. Subjects are instructed to stand with both feet positioned inside the boundaries of the starting box. The test initiates when the subject begins to reach in one of the four diagonal directions.

Standing Jump. Subjects are placed their feet shoulder-width apart and toes placed in a line on the floor. The subjects then made a horizontal leap forward, where they were allowed the arms to swing, and it will be done along the length of a tape measure that was fixed to the ground. The subjects had to stick to the ground in the landing phase, preventing any additional movement of the feet when landing.

The jumped distance will be calculating as the distance from the jump initiation line to the heel of the back foot. The best of three attempts was recorded, with a recovery of 60 seconds between attempts. All distances will be measuring with an accuracy of 0.01 meters.

Secondary outcome:

Impression of Change (CGI). Patient Global Impression of Change Scale (PGIOCS) that evaluates the change perceived by the subject after a treatment. This scale has 7 affirmations to choose from (I have improved a lot, quite, a little, I am the same, I have worsened a little, a lot or a lot) and a pain analogue scale of 10 cm.

02

Conditions studied

  • Athletic Injuries

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03

In context

Athletic Injuries

270 studies on the registry are indexed under Athletic Injuries; 42 are open to participants now.

This study's enrollment of 45 is above the median of 40 across 165 interventional studies indexed under Athletic Injuries.

Browse Athletic Injuries studies →

Lead sponsor

University of Valencia is the lead sponsor of 349 studies on the registry; 73 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • male and female amateur athletes

Exclusion criteria

Exclusion Criteria:

  • previous surgery of the locomotor system in lower limbs
  • musculoskeletal injuries in any part of the body that prevent practicing sports understanding or communication difficulties
  • insufficient fluency in the Spanish language to follow measurement instructions.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
45 participants (actual)

Study arms

  • Active comparator
    Foam Rolling Group (FR)

    Other: Foam Rolling (FR)

  • Active comparator
    Orthopaedic Manual Physical Therapy Group (OMPT)

    Other: Orthopaedic Manual Physical Therapy Group (OMPT)

  • Other
    Control Group (CG)

    Other: Control Group (CG)

Interventions

  • OtherFoam Rolling (FR)

    FR auto-massage will place the foam roller between their ischial tuberosity and a hard surface (i.e., the floor) with their legs held in an extended position, keeping their ankles relaxed and oriented upward. For FR in the lumbar region, participants use their weight to slide the FR through the erector of the lumbar and thoracic spine. The total approximate duration will be about 10-15 minutes.

  • OtherControl Group (CG)

    The CG did not receive any intervention.

  • OtherOrthopaedic Manual Physical Therapy Group (OMPT)

    Based on the protocol used by Espí-López et al.: a) Unspecific and bilateral lumbar thrust (L5-S1), one of each side were performed; b) Hip joint decompression, performing 25 repetitions c) Hip rotator stretch with hip and knee flexion, 15 repetitions; d) Femorotibial decompression, 25 reps. e) Quadriceps femoral muscle compression and traction, 25 repetitions; f) Opening of the internal and external femorotibial interline, 15 repetition; g) Ankle decompression, 3 repetitions; h) Posteroanterior and anteroposterior mobilization of head and base of fibula, 25 repetitions. The total duration will be approximately 10-15 minutes.

06

What researchers measure

Primary outcomes

  1. Dynamic balance

    Dynamic balance using the Star Excursion Balance Test (SEBT). The SEBT is a dynamic test that requires strength, flexibility, and proprioception. The goal of the SEBT is to maintain single-leg stance while reaching as far as possible with the contralateral leg. Subjects are instructed to stand with both feet positioned inside the boundaries of the starting box. The test initiates when the subject begins to reach in one of the four diagonal directions.

    Time frame: 1 day

Secondary outcomes

  1. Perception of Change

    Patient Global Impression of Change Scale (PGIOCS) that evaluates the change perceived by the subject after a treatment. This scale has 7 levels which represent improvement from 1 to 3, 4 indicates no change and 5 to 7 indicates worsening. In addition, it includes a visual analog scale which scores range from 0 to 10 where 0 is much better and 10 much worse.

    Time frame: 1 day

  2. Lumbar flexibility

    Modified Schober test (MMST). The MMST was designed to assess the mobility of the entire lower back, so the MMST was used to measure lumbar flexion before and after FR and TM interventions. The examiner will place his thumbs on the lower margin of the posterior-upper iliac spine (lower reference point) and a pen mark was made. While the examiner held the tape against the subject's skin, another signal was marked 15 cm above the first (upper reference point). Each subject was then asked to perform an active flexion of the entire trunk and the distance between the two points will be measuring and then the subject return to his initial position. The difference between the initial distance and the new bending measurements will be take.

    Time frame: 1 day

  3. Hip flexion

    Hip flexion by the passive straight leg raise (SLR). Passive SLR will be conducting using a procedure previously described by Hopper et al. A Richards splint and an ankle foot orthosis were applied to the left leg to maintain the knee in full extension and the ankle at a neutral plantar angle. An inclinometer will be attaching to a belt, which will place around the pelvis at the level of the anterior superior iliac spine (Baseline Bubble Inclinometer. Fabrication Enterprises, PO Box, 1500 White Plains, NY 10602, USA). A second inclinometer will be then attaching to the Richards splint at the level of the knee joint line. The mean of 3 measures will be using for analysis. During the test, the participants are positioned with their hands on the abdomen, cervical spine in a neutral position and eyes closed.

    Time frame: 1 day

  4. Standing Jump

    Subjects are placed their feet shoulder-width apart and toes placed in a line on the floor. The subjects then made a horizontal leap forward, where they were allowed the arms to swing, and it will be done along the length of a tape measure that was fixed to the ground. The subjects had to stick to the ground in the landing phase, preventing any additional movement of the feet when landing. The jumped distance will be calculating as the distance from the jump initiation line to the heel of the back foot. The best of three attempts was recorded, with a recovery of 60 seconds between attempts. All distances will be measuring with an accuracy of 0.01 meters.

    Time frame: 1 day

07

Study locations

1 site
  • Gemma v. Espí López
    Valencia, 46010, Spain
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 2, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04161300
Lead sponsor
University of Valencia
Responsible party
GEMMA V ESPÍ LÓPEZ, PhD (Principal Investigator, University of Valencia) — Principal investigator
First posted
Nov 13, 2019
Start date
Nov 15, 2019
Primary completion
Jan 15, 2020
Completion
Feb 18, 2020
Last update
Mar 2, 2021

Study contacts

Gemma V Espí-López, Dr
principal investigator · Faculty of Physiotherapy. University of Valencia

Oversight

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

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