Plantar Fascia Release With Magnetic Fascia Ball

Sponsor
Abant Izzet Baysal University (Other)
Overall Status
Completed
CT.gov ID
NCT06034704
Collaborator
(none)
32
1
2
4
8

Study Details

Study Description

Brief Summary

In this study, the effect of plantar fascia release with a magnetic fascial cork ball on hamstring and lumbar extensor muscle elasticity will be investigated.

Condition or Disease Intervention/Treatment Phase
  • Other: Plantar fascia self massage with a magnetic fascia ball
  • Other: Plantar fascia self massage with a non-magnetic fascia ball
N/A

Detailed Description

The use of tools such as foam rollers or massage balls to resolve myofascial tension is highly preferred by both therapists and patients. It is theorized that the sweeping pressure generated during rolling causes the fascia to stretch and increase the range of motion. In addition, the warming caused by the friction during rolling can dissolve the adhesions between the fascial layers and restore the elasticity of the myofascial tissues. In addition to similar mechanical effects, the use of cork balls with magnetic properties is becoming increasingly common. Studies have shown that static magnetic magnets reduce pain, increase microcirculation and oxygenation and cause changes in presynaptic membrane function. As far as we know, there is no study examining the myofascial relaxation effect of magnetic balls in the literature. Evaluating the clinical impact and efficacy of this device which allow the person to perform self-massage might contribute the current literature. This study was planned to evaluate the myofascial relaxation caused by two different fascial cork balls with and without magnetic properties.

Study Design

Study Type:
Interventional
Actual Enrollment :
32 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Investigation of the Effect of Plantar Fascia Release With Magnetic Fascia Ball on Hamstring and Lumbar Spine Flexibility
Actual Study Start Date :
Jun 1, 2021
Actual Primary Completion Date :
Sep 30, 2021
Actual Study Completion Date :
Sep 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Magnetic Fascial Ball

In the experimental group, a fascial ball made of cork containing 3 magnets of 0.15 tesla was used. The magnetic fascia ball diameter is 6 centimetres.

Other: Plantar fascia self massage with a magnetic fascia ball
Participants were asked to roll the magnetic fascia ball on the sole of each foot for 3 minutes each, from the metatarsal heads towards the heel, concentrating on the medial longitudinal arch. Participants were informed that more intense pressure would be more beneficial and were asked to apply pressure in a way that would not cause pain.

Placebo Comparator: Non-Magnetic Fascial Ball

In the placebo group, a fascial ball made of cork without magnets. The non-magnetic fascia ball diameter is 6 centimetres.

Other: Plantar fascia self massage with a non-magnetic fascia ball
Participants were asked to roll the non-magnetic fascia ball on the sole of each foot for 3 minutes each, from the metatarsal heads towards the heel, concentrating on the medial longitudinal arch. Participants were informed that more intense pressure would be more beneficial and were asked to apply pressure in a way that would not cause pain.

Outcome Measures

Primary Outcome Measures

  1. Goniometric Measurement of Hamstring Flexibility [Two times in one day (before intervention, immediately after intervention)]

    Individuals are positioned supine with the hip of the limb to be measured at 90 degrees. In this position, active knee extension is requested and the acute angle between the long axis of the femur and the long axis of the fibula is measured. The DrGonyometer (iOS) smart phone application, for which a validity and reliability study was conducted, was used for the measurement.

Secondary Outcome Measures

  1. Sit and reach test [Two times in one day (before intervention, immediately after intervention)]

    Individuals are placed in a long sitting position with their feet resting on the test battery (Figure 2) and knees in full extension. They are asked to reach forward on the wooden block by placing their hands on top of each other. In this position, the distance between the fingers of the hand and the point where the foot rests is measured and the previous values are recorded as negative and the following values as positive.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Having scored 3 or less according to the Beighton scoring system

  • 18-35 years old,

  • Having asymptomatic

  • Voluntary participation in the research

Exclusion Criteria:
  • Having Beighton score of 4 and above

  • Having history of previous surgery

  • Having diagnosed pathology of the lower extremities and lumbar region

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of Health Sciences Bolu Abant İzzet Baysal University Bolu Turkey 14300

Sponsors and Collaborators

  • Abant Izzet Baysal University

Investigators

  • Principal Investigator: Ömer Osman PALA, Bolu Abant İzzet Baysal Üniversitesi

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ömer Osman Pala, Assistant Professor, Abant Izzet Baysal University
ClinicalTrials.gov Identifier:
NCT06034704
Other Study ID Numbers:
  • AIBU-FTR-OOP-1
First Posted:
Sep 13, 2023
Last Update Posted:
Sep 13, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ömer Osman Pala, Assistant Professor, Abant Izzet Baysal University

Study Results

No Results Posted as of Sep 13, 2023