The Acute Effect of Foam Rolling on Elbow Joint Sensorimotor Function

February 11, 2019 updated by: Fatma Özden, PT, Dokuz Eylul University
The purpose of this study is to investigate the acute effects of foam rolling on elbow joint sensorimotor function with healthy participants . Study group will receive foam rolling exercise. Control group will receive no foam rolling exercise. Control group will be given a brochure including information about proprioception and foam rolling.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

There is no information in literature about the effects of foam rolling on elbow joint sensorimotor function. The purpose of this study is to investigate acute effects of foam rolling with healthy participants. Study group will receive foam rolling exercise actively by themselves on elbow.

Foam rolling exercise will be applied 10 times each for 1 minute. These exercise will be performed as 2 sets. After each set will be a resting period for 30 seconds. A total of 1 session will be performed. Second evaluation will be performed after exercise at the same day. Control group will receive no foam rolling exercise. They will be handed a brochure about the proprioception and its role in injury prevention and foam rolling. Control group will be evaluated for the first time. Afterwards, second evaluation will be performed after resting period (2 minutes) at the same day.

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Bornova
      • İzmir, Bornova, Turkey, 35090
        • Fatma Özden

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 18 years and above healthy participants
  • No pain in elbow area within 6 months and at the time of measurement
  • To be able to complete all evaluations and applications to be carried out

Exclusion Criteria:

  • Having previous foam rolling and self-myofascial relaxation applications on the target area
  • Having acne and similar skin problems, open wounds
  • Having upper extremity injury, history of fracture or surgery
  • Having any systemic musculoskeletal disease
  • Having diagnosis of diabetic mellitus or peripheral neuropathy
  • Having osteoporosis diagnosis
  • Having any cardiovascular disease
  • Having vertigo
  • Being pregnant

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Foam Rolling Group
The participants in this group will receive foam rolling exercise.
Foam rolling exercise will be performed actively. Participants will use a foam roller for exercise. They will position the foam roller on the chair. Afterwards, they will use their body weights to rub the elbow area (biceps brachii muscle) with this foam. There will be 2 sets and each set will be 1 minute. Single set contains 10 repetitions in 1 minute with 30 seconds resting period between sets
No Intervention: Control Group
The participants in this group will receive no foam rolling. They will only be evaluated.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Elbow Proprioception
Time Frame: [Time Frame: Baseline, after 1session foam rolling exercise period and then follow up measurement at the same day]
Change of elbow joint position sense (with digital inclinometer in degree ) and force match ( hand held dynamometer in kg )
[Time Frame: Baseline, after 1session foam rolling exercise period and then follow up measurement at the same day]

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Biceps Brachii Strength
Time Frame: [Time Frame: Baseline, after 1session foam rolling exercise period and then follow up measurement at the same day]
Change of biceps brachii strength ( hand held dynamometer in kg )
[Time Frame: Baseline, after 1session foam rolling exercise period and then follow up measurement at the same day]
Elbow Sensorimotor Performance
Time Frame: [Time Frame: Baseline, after 1session foam rolling exercise period and then follow up measurement at the same day]
Change of elbow functional motor performance (push up test, modified pull up test, closed kinetic chain upper extremity stability test )
[Time Frame: Baseline, after 1session foam rolling exercise period and then follow up measurement at the same day]

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 20, 2018

Primary Completion (Actual)

October 20, 2018

Study Completion (Actual)

November 20, 2018

Study Registration Dates

First Submitted

April 24, 2018

First Submitted That Met QC Criteria

April 24, 2018

First Posted (Actual)

May 4, 2018

Study Record Updates

Last Update Posted (Actual)

February 12, 2019

Last Update Submitted That Met QC Criteria

February 11, 2019

Last Verified

February 1, 2019

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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