Effectiveness of the Suboccipital Inhibition Technique in Patients With Mechanical Neck Pain

University of Alcala

Status: Unknown

Conditions: Myofascial Pain; Neck Pain

Treatments: Other: Suboccipital inhibition technique

Study type: Interventional

Funder types: Other

Identifiers

NCT02890394

UAH

Details and patient eligibility

About

The project is based on checking the effectiveness of the technique of suboccipital inhibition in patients with mechanical neck pain. Suboccipital inhibition technique involves the placement of the hands of the physiotherapist under the patient's head so that fingers can feel the spinous processes of the cervical vertebrae. Then the fingers slowly leads upward to contact the occipital condyles. At this point the investigator should gently move your fingers down, finding the space between the condyles and the spinous process of the axis. Then, flexing the metacarpophalangeal joints at 90 degrees, slowly raises the skull. In this technique the investigator would be carrying out the relaxation of the suboccipital muscles: lower rectus capitis posterior, superior oblique head straight back and head higher. It is a technique used very often but without knowledge about the time needed for implementation. In several studies that have used the technique it has been maintained for 2.4 or 10 minutes without agreeing how long is necessary. The study will consist of three groups formed by patients with mechanical neck pain that they applied the technique two, four or ten minutes and a control group of patients with mechanical neck pain. The four groups were measured before and after treatment the pain threshold to pressure by algometer and conduct the test repositioning of the head to show any changes after application of the technique.

Enrollment: 60 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Men and women of full age .
2. ≥ 15/50 rating in the Neck Disability Index
3. Participants with good adhesion to the study .
4. Participants who have signed informed after appropriate informed consent.

Exclusion criteria

1. Cancer , inflammatory , infectious , vascular , neurological and metabolic processes.
2. Patients who are under medical treatment.
3. Patients with psychiatric illnesses.
4. Women : pregnancy.
5. Patients who have not signed the informed consent.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: Single Blind

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60 participants in 4 patient groups

2 minutes Group

Experimental group

Description:

The group was perform the technique inhibition suboccipital two minutes, collecting data by measuring with algometer and test repositioning of the head before and after the technique.

Treatment:

Other: Suboccipital inhibition technique

4 minutes Group

Experimental group

Description:

The group was perform the technique inhibition suboccipital four minutes, collecting data by measuring with algometer and test repositioning of the head before and after the technique.

Treatment:

Other: Suboccipital inhibition technique

8 minutes Group

Experimental group

Description:

The group was perform the technique inhibition suboccipital eight minutes, collecting data by measuring with algometer and test repositioning of the head before and after the technique.

Treatment:

Other: Suboccipital inhibition technique

not intervention Group

No Intervention group

Description:

The not intervention group will be asked to lie supine on the table for ten minutes, collecting data by measuring with algometer and test repositioning of the head before and after laying.