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The Acute Effect of Foam Rolling on Elbow Joint Sensorimotor Function

Primary Purpose

Proprioceptive Disorders

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Foam Rolling Exercise
Sponsored by
Dokuz Eylul University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Proprioceptive Disorders focused on measuring elbow, foam rolling, proprioception, sensorimotor, acute

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Fatma Özden

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Foam Rolling Group

Control Group

Arm Description

The participants in this group will receive foam rolling exercise.

The participants in this group will receive no foam rolling. They will only be evaluated.

Outcomes

Primary Outcome Measures

Elbow Proprioception
Change of elbow joint position sense (with digital inclinometer in degree ) and force match ( hand held dynamometer in kg )

Secondary Outcome Measures

Biceps Brachii Strength
Change of biceps brachii strength ( hand held dynamometer in kg )
Elbow Sensorimotor Performance
Change of elbow functional motor performance (push up test, modified pull up test, closed kinetic chain upper extremity stability test )

Full Information

First Posted
April 24, 2018
Last Updated
February 11, 2019
Sponsor
Dokuz Eylul University
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1. Study Identification

Unique Protocol Identification Number
NCT03516149
Brief Title
The Acute Effect of Foam Rolling on Elbow Joint Sensorimotor Function
Official Title
The Acute Effect of Foam Rolling on Elbow Joint Sensorimotor Function
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
August 20, 2018 (Actual)
Primary Completion Date
October 20, 2018 (Actual)
Study Completion Date
November 20, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dokuz Eylul University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Proprioceptive Disorders
Keywords
elbow, foam rolling, proprioception, sensorimotor, acute

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
There are 2 groups. Study group will receive foam rolling exercise. 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 . Study group will be evaluated before foam rolling exercise . Afterwards, second evaluation will be performed after exercise at the same day. Control group will be evaluated for the first time. Afterwards, second evaluation will be performed after resting period (2 minutes) at the same day.
Masking
Participant
Masking Description
All of participants must be healthy.
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Foam Rolling Group
Arm Type
Experimental
Arm Description
The participants in this group will receive foam rolling exercise.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
The participants in this group will receive no foam rolling. They will only be evaluated.
Intervention Type
Other
Intervention Name(s)
Foam Rolling Exercise
Intervention Description
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
Primary Outcome Measure Information:
Title
Elbow Proprioception
Description
Change of elbow joint position sense (with digital inclinometer in degree ) and force match ( hand held dynamometer in kg )
Time Frame
[Time Frame: Baseline, after 1session foam rolling exercise period and then follow up measurement at the same day]
Secondary Outcome Measure Information:
Title
Biceps Brachii Strength
Description
Change of biceps brachii strength ( hand held dynamometer in kg )
Time Frame
[Time Frame: Baseline, after 1session foam rolling exercise period and then follow up measurement at the same day]
Title
Elbow Sensorimotor Performance
Description
Change of elbow functional motor performance (push up test, modified pull up test, closed kinetic chain upper extremity stability test )
Time Frame
[Time Frame: Baseline, after 1session foam rolling exercise period and then follow up measurement at the same day]

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sevgi Sevi Yeşilyaprak, Phd
Organizational Affiliation
Dokuz Eylul University
Official's Role
Study Director
Facility Information:
Facility Name
Fatma Özden
City
İzmir
State/Province
Bornova
ZIP/Postal Code
35090
Country
Turkey

12. IPD Sharing Statement

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The Acute Effect of Foam Rolling on Elbow Joint Sensorimotor Function

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