The Acute Effect of Foam Rolling on Elbow Joint Sensorimotor Function

NCT ID: NCT03516149

Last Updated: 2019-02-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-08-20

Study Completion Date

2018-11-20

Brief Summary

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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

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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.

Conditions

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Proprioceptive Disorders

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
All of participants must be healthy.

Study Groups

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Foam Rolling Group

The participants in this group will receive foam rolling exercise.

Group Type EXPERIMENTAL

Foam Rolling Exercise

Intervention Type OTHER

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

Control Group

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

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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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

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Dokuz Eylul University

OTHER

Sponsor Role lead

Responsible Party

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Fatma Özden, PT

Physical Therapist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Sevgi Sevi Yeşilyaprak, Phd

Role: STUDY_DIRECTOR

Dokuz Eylul University

Locations

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Fatma Özden

Izmir, Bornova, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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3470-GOA

Identifier Type: -

Identifier Source: org_study_id

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