The Effectiveness of Exercises Protocol in Management of Neck Pain
NCT ID: NCT02225873
Last Updated: 2015-12-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2014-09-30
2015-01-31
Brief Summary
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Hypothesis: The craniocervical flexion (motor control) and muscle strength training protocol will improve muscle function more than the proprioception and muscle strength protocol in patients with chronic cervical pain.
Objective: To find out if applying the strength therapeutic exercise protocol and the craniocervical flexion coordination (motor control) training is more effective than the strength and articular repositioning protocol when carrying out the craniocervical flexion test in patients with chronic cervical pain.
Detailed Description
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This study will verify whether the cranio-cervical flexion coordination (motor control) and muscle strength training protocol is more effective in improving muscle than the proprioception and muscle strength protocol in patients with chronic neck pain.
The project design will be a randomized controlled evaluator-blinded clinical trial with two intervention groups:
Group 1 (experimental) will carry out motor control exercises through cranio-cervical flexion training and strength-endurance exercises.
Group 2 (control) will carry out exercises to improve muscle strength-endurance and proprioception. Measurements will be done at the beginning of the study, pre and post-treatment, one month and two months after treatment and throughout the six month treatment. Each session will last 45 minutes and therapy will be performed without provoking the patient symptoms.
Intervention
Experimental group 1: will carry out intermuscular coordination exercises through cranio-cervical training, following Jull et al1, 2 and exercises to increase strength-endurance on the neck flexor muscles.
Control group 2: will carry out proprioception exercises through articular repositioning training and exercises to increase strength-endurance on the neck flexor muscles. They will be performed in the same way as the experimental group protocol.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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strength-endurance exercises
Group 1 (experimental) will carry out motor control exercises through cranio-cervical flexion training and strength-endurance exercises.
motor control exercises
Will carry out intermuscular coordination exercises through cranio-cervical training, following Jull et al. and exercises to increase strength-endurance on the neck flexor muscles
strength-endurance and proprioception
Group 2 (control) will carry out exercises to improve muscle strength-endurance and proprioception.
muscle strength-endurance and proprioception
Will carry out proprioception exercises through articular repositioning training and exercises to increase strength-endurance on the neck flexor muscles. They will be performed in the same way as the experimental group protocol.
Interventions
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motor control exercises
Will carry out intermuscular coordination exercises through cranio-cervical training, following Jull et al. and exercises to increase strength-endurance on the neck flexor muscles
muscle strength-endurance and proprioception
Will carry out proprioception exercises through articular repositioning training and exercises to increase strength-endurance on the neck flexor muscles. They will be performed in the same way as the experimental group protocol.
Eligibility Criteria
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Inclusion Criteria
* Between 18 and 55 years old.
* Altered movement and/or loss of cervical control.
* Pain after palpation of the muscles to be treated.
Exclusion Criteria
* Previous surgery of the cervical, cranial, scapular waist, upper limb or jaw.
* Having received specific treatment or therapy of the cervical region in the 6 months prior to the study.
* Neck pain or headache with no musculo-skeletal causes.
* Any other disorder that prevents physical activity.
* Having received psychological treatment due to neck pain.
* Patients with fibromyalgia, rheumatoid arthritis, vascular diseases, neoplasm or vestibular system pathologies.
18 Years
60 Years
ALL
No
Sponsors
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University of Alcala
OTHER
Responsible Party
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Prof. Dr. Daniel Pecos Martín
Dr.
Principal Investigators
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Tomas Gallego-Izquierdo, Dr
Role: STUDY_CHAIR
Alcala University
Locations
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Alcalá University
Alcalá de Henares, Madrid, Spain
Countries
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Other Identifiers
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M2013/046/20140528
Identifier Type: -
Identifier Source: org_study_id