Skip to content

Electroencephalography Activity in Individuals With Nonspecific Chronic Low Back Pain After Cranial Osteopathic Manipulative Treatment

Electroencephalography Activity in Individuals With Nonspecific Chronic Low Back Pain After Cranial Osteopathic Manipulative Treatment: Study Protocol of a Randomized, Controlled Crossover Trial

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02111382
Enrollment
0
Registered
2014-04-11
Start date
2018-01-31
Completion date
2018-12-31
Last updated
2023-08-15

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

Conditions

Low Back Pain

Keywords

Low back pain, osteopathic manipulations, electroencephalography

Brief summary

Osteopathic medicine is based on a diagnostic and therapeutic system to treat tissue mobility/ motility dysfunctions in general, using different approaches (depending on the target tissue) known as osteopathic manipulative treatment. Among all the available techniques those ones addressed to the cranial field are most questioned because of the lack of scientific evidence; but the compression of the 4th ventricle technique has been largely studied in clinical trials. Studies have shown that the technique may affect both central and autonomous nervous system, modulating some reflexes (Traube-Hering baro signal), and modifying brain cortex electrical activity through central sensitization in subjects with chronic low back pain. Thus, investigators hypothesize that the compression of the 4th ventricle may modulate peak alpha frequency (electroencephalographic assessment) and promote physical relaxation in subjects in vigil.

Detailed description

A randomized controlled crossover trial with blinded assessor was designed to test the hypothesis. A total of 81 participants will be assigned to three treatment conditions, with seven days of washout: compression of the 4th ventricle group; sham compression of the 4th ventricle group; control group (no intervention). All participants will be recruited at the Outpatient Rehabilitation Service of the University Hospital of Brasília - University of Brasília (Brazil).

Interventions

OTHERCV4 Cranial (4th ventricle technique) Osteopathic Manipulative

The participant will be in supine position during the whole procedure. The practitioner sits behind the participant's head, contacts participant's lateral protuberances of the squama occipitalis (medially to the occipitomastoid suture) with the thenar eminence of both hands. When the practitioner feels the PRM (a pulsating rhythm caused by liquor production and reabsorption), the flexion phase will be resisted and the extension phase exaggerated. The compressive force is held until the PRM stops (event known as 'Still point'). The compression will be held until the practitioner feels PRM gradual return; the compression will be slowly diminished, and then, the practitioner remove the hands from the occipital bone, laying the participant's head on the table. The CV4 technique will be performed by an osteopath D.O. - member of the Brazilian Register of Osteopaths.

OTHERCV4 (4th ventricle technique) manual therapy sham technique

The participant will be in supine position and the practitioner will be seated behind the participant's head. The practitioner places the fingers (2nd to 5th) under the occipital bone, touching only the squama occipitalis. The practitioner will hold this position for 5 minutes, and after this period the participant's head will be placed on the table. The CV4 sham will be performed by a registered physiotherapist.

Sponsors

University Hospital of Brasília
CollaboratorUNKNOWN
University of Brasilia
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participants over 18 years old with self-reported nonspecific chronic low back pain will be recruited

Exclusion criteria

* Participants suffering from secondary chronic low back pain, * fever, chills, sweating, weight loss, asthenia, anorexia; * cardiovascular and respiratory symptoms such as chest pain, dyspnea and cough; * headache, dizziness, lightheadedness, fainting, tremors, dysarthria and aphasia; * participants who underwent surgery on the spine; * diagnosis of any neurological, cardiac, respiratory and rheumatic disease; * regular use of drugs with effects on the central nervous system.

Design outcomes

Primary

MeasureTime frameDescription
Peak alpha frequency (Electroencephalography)Baseline, 10 minutes.Baseline: before intervention. 10 minutes: 10 minutes after intervention.

Secondary

MeasureTime frameDescription
Pain intensityBaseline, 10 minutesBaseline: before intervention. 10 minutes: 10 minutes after intervention. Pain intensity: 0-10 Numeric Pain Rating Scale

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026