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Suboccipital Myofascial Release Technique in Young Adults

Investigation of the Instant Effects of the Suboccipital Myofascial Release Technique on Cervical Proprioception, Joint Range of Motion and Balance in Young Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06105385
Enrollment
25
Registered
2023-10-27
Start date
2023-10-12
Completion date
2023-11-12
Last updated
2024-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myofascial Release

Keywords

Suboccipital Myofascia, Release Technique, Cervical Proprioception, Range of Motion, Balance

Brief 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.

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.

Sponsors

Pamukkale University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Joint Position Error MeasurementBefore and Immediately After the Treatment ProcessThe 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.
Cervical Joint Range of Motion MeasurementBefore and Immediately After the Treatment ProcessCervical joint movement, cervical flexion, extension, right and left rotation, right-left lateral flexion movement will be measured with the help of a suitable goniometer.
Balance AssessmentBefore and Immediately After the Treatment ProcessPortable 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026