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CompletedNCT06105385Updated Apr 4, 2024

Suboccipital Myofascial Release Technique in Young Adults

An interventional study of Suboccipital Myofascial Release Technique in Myofascial Release, sponsored by Pamukkale University. Completed at 1 site in Turkey. Open to participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-04-04.

Sponsored by Pamukkale University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
25
Allocation
Non-randomized
Ages
18 Years to 25 Years
Sex
All
01

Study summary

When the literature is examined, although it is known that the suboccipital muscles are rich in proprioceptive receptors and have significant effects on balance, the effects of myofascial and neural relaxation of the suboccipital muscles on balance and proprioception are not fully understood. In this study, the investigators aim to examine the immediate effects of the SMV technique on balance and proprioception in young adults. With this study, by revealing the effects of the SMV technique on balance and proprioception, a different treatment option will be offered to clinicians working in the field of physical therapy and rehabilitation and interested in the rehabilitation of patients who may have balance and proprioception problems. It will also provide insight to academics working in this field in terms of the applicability of this technique among different patient groups.

02

Conditions studied

  • Myofascial Release

Keywords

  • Suboccipital Myofascia
  • Release Technique
  • Cervical Proprioception
  • Range of Motion
  • Balance
03

In context

Lead sponsor

Pamukkale University is the lead sponsor of 331 studies on the registry; 61 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Being between the ages of 18-25
  • Being healthy and not having one of the diseases specified in the exclusion criteria

Exclusion criteria

Exclusion Criteria:

  • Individuals with neck pain, neck trauma (fracture, whiplash syndrome), balance and proprioception problems, vestibular system problems, vertigo, cervical surgery, vision and hearing problems, any rheumatological, orthopedic, cardiovascular and neurological problems that may affect the cervical region
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
25 participants (actual)

Study arms

  • Experimental
    First

    Suboccipital Myofascial Release Technique will be applied to this group first. After the intervention in this group is completed, the transition to the other crossover group will be made.

    Other: Suboccipital Myofascial Release Technique

  • Experimental
    Second

    Once the intervention to the first group is completed, the second intervention "Suboccipital Myofascial Release Technique" will be applied to this group.

    Other: Suboccipital Myofascial Release Technique

Interventions

  • OtherSuboccipital Myofascial Release Technique

    With the patient in a supine position, the therapist sits behind the patient with his or her forearms on the treatment table. The therapist places his fingers between the occiput and axis, with his fingers in semi-flexion (2nd, 3rd and 4th fingers), and continues to hold his hands on the occiput until relaxation is achieved in the suboccipital muscles. A light traction is applied at the end of the technique. Average application time is 4-5 minutes.

06

What researchers measure

Primary outcomes

  1. Joint Position Error Measurement

    The Cervical Joint Position Error Test is a measurement tool used to clinically assess an individual's cervicocephalic proprioception ability. Cervicocephalic proprioception describes one's sense of position of their head and neck in space.

    Time frame: Before and Immediately After the Treatment Process

  2. Cervical Joint Range of Motion Measurement

    Cervical joint movement, cervical flexion, extension, right and left rotation, right-left lateral flexion movement will be measured with the help of a suitable goniometer.

    Time frame: Before and Immediately After the Treatment Process

  3. Balance Assessment

    Portable computerized kinesthetic balance device (SportKAT) examines balance in 2 main parameters: static and dynamic, and 4 main parameters: forward-backward, right-left. SporKAT consists of a platform on the ground and a screen designed to be directly in front of the patient, 1 meter away from the patient. After the pressure values of the platform are adjusted, the content of the test is explained to the patient and the patient is placed on the platform with bare feet, and then the patient's feet are adjusted to the specified places on the platform. During the test, the patient is asked to try to keep the x (cross) sign on the screen in the middle of the circle visible on the screen for 30 seconds. The test is terminated after 30 seconds. Higher balance scores indicate that the person's balance is more impaired.

    Time frame: Before and Immediately After the Treatment Process

07

Study locations

1 site
  • Pamukkale University
    Denizli, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 4, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06105385
Lead sponsor
Pamukkale University
Responsible party
Fatih Tekin (Assist. Prof., Pamukkale University) — Principal investigator
First posted
Oct 27, 2023
Start date
Oct 12, 2023
Primary completion
Nov 1, 2023
Completion
Nov 12, 2023
Last update
Apr 4, 2024

Study contacts

Fatih Tekin, Ass. Prof.
study chair · Faculty Member

Oversight

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

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