Hypoalgesic Effect of Neural Mobilization

NCT02595294 | Completed DMC

• 2 other identifiers: CE0072015-2CE0072015
• Study Type: interventional
• Target: 52
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of these study is to compare the effectivity of the Cervical Lateral Glide physical therapy neural mobilization technique to the complete absence of treatment in a group of patients who suffer cervicobrachial pain.

Conditions

Cervicobrachial Neuralgia

Outcome Measures

Primary Outcomes (1)

• Change from baseline using the Numeric Rating Scale for Pain at 1 hour

  the Numeric Rating scale for Pain (NRS) is an 11 point scale for patient self reporting of pain in which 0 points represents the total absence of pain and 10 points the worst state of pain, it was employed to evaluate the presence and relieve of cervicobrachial pain symptoms.

  at baseline for both arms and 1 hour after the application of treatment only in the experimental arm, corresponding to intervention days 1, 15 and 30

Secondary Outcomes (2)

• Change from baseline of the Physical function involving the affected upper limb using the Quik DASH Scale

  at baseline, corresponding to intervention days 1 and 30 of treatment

• Cervical Rotation Range of Motion (CROM)

  at baseline for both arms and 1 hour after the application of treatment only in the experimental arm, corresponding to intervention days 1 and 30

Study Arms (2)

Cervical Lateral Glide

EXPERIMENTAL

* 15 minutes Cervical Lateral Glide neural mobilization * 5 times a week * During 6 weeks * Patient's adequate cervical spine linear alignment was determined through the baseline use of a Universal Goniometer Device in each application of Cervical Lateral Glide neural mobilization.

Procedure: Cervical Lateral Glide neural mobilization

Waiting list control group

NO INTERVENTION

\- Patients assigned to a 6 week waiting list to receive treatment

Interventions

Cervical Lateral Glide neural mobilization PROCEDURE

Non-surgical non-invasive Cervical Lateral Glide neural mobilization procedure was applied by a physical therapist continuously during 2 minutes in 5 different occasions with 1 minute of rest between each 2 minute application of the Neural Mobilization technique. The intervention was applied during a period of 6 weeks. The correct linear alignment of patient's cervical spine was determined through the baseline use of a Universal Goniometer Device in each application of Cervical Lateral Glide neural mobilization.

Also known as: Cervical Lateral Glide Neural Tissue Mobilization, Cervical Lateral Glide Neurodynamics

Cervical Lateral Glide

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Clinical diagnosis of cervicobrachial pain confirmed by magnetic resonance imaging
• Presence of unilateral symptoms of arm pain, paresthesia or numbness in the upper extremity during at least 3 continuous months previous to the application of treatment.
• Positive results in all of the following tests: Spurling, Distraction, and Upper Limb

You may not qualify if:

• Contraindication in the use of nonsteroidal anti inflammatory drugs (NSAIDs)
• The use of any type of treatment, therapy, procedure or drug to relieve pain
• Patients who are under anticonvulsant, antidepressant or psychotropic medication
• Vertebral instability
• Vertebral osteoporosis
• Vertebral or spine infection.
• Neurologic diseases of genetic, infectious or neoplastic origin
• Cervical stenosis myelopathy
• Pregnancy
• Kinesiophobia
• Endocrine disorders and menopause
• History of spine surgery
• Intellectual disability, severe mental illness, intoxication, severe sleep deprivation, Alzheimer's disease.

Sponsors & Collaborators

• Universidad Europea de Madrid: lead

Study Sites (1)

"Centro Médico y de Especialidades Pediátricas Dr. José Gregorio Hernández "

San Diego, Carabobo, 02006, Venezuela

Location

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Related Links

• DASH Outcome Measure Institute for Work \& Health

MeSH Terms

Conditions

Brachial Plexus Neuritis

Condition Hierarchy (Ancestors)

Brachial Plexus Neuropathies; Peripheral Nervous System Diseases; Neuromuscular Diseases; Nervous System Diseases; Neuritis

Study Officials

• Francisco H Unda, PT, MSc

  Universidad Europea de Madrid

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: PHD Student

Study Record Dates

• First Submitted: October 26, 2015
• First Posted: November 3, 2015
• Study Start: July 1, 2015
• Primary Completion: October 1, 2015
• Study Completion: October 1, 2015
• Last Updated: October 4, 2019

Record last verified: 2019-10

Locations

VE (1)