- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01792895
Different Types of Manual Therapy Techniques in Patients With Chronic Neck Pain (CNP)
Is Better the One Type of Manual Therapy Than Others for to Treat the Patients With Chronic Neck Pain? : A Randomized Clinical Trial
The purpose of this study was to investigate the comparative effectiveness of high velocity and low amplitude (HVLA)vs Mobilization (Mob) vs Mobilization with movement technique (MWMT) in sample of patients with chronic neck pain (CNP). Secondly to evaluate the immediate effects in range of motion and pain thresholds, and the interaction between psychological factors and the outcomes of these three types of manual therapy.
The hypothesis is that all manual therapies techniques will produce similar effects.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Madrid
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Alcorcon, Madrid, Spain, 28922
- Universidad Rey Juan Carlos
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Clinical Diagnosis of Chronic neck pain
Exclusion Criteria:
- Neck pain is associated with whiplash injuries.
- Resting blood pressure greater than 140/90 mmHg.
- Cervical radiculopathy.
- Cervical disc herniation.
- Fibromyalgia syndrome.
- Previous neck surgery.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Manipulation group
This Technique will be applied over four sessions, during two weeks
|
The mobilization is a passive oscillatory technique, applied over cervical region in the hypomobile cervical level, the patient will be in prone and the therapist standing at the head of the patients with his thumbs in opposition placed at the level of the facet of the hypomobile cervical vertebra.
A posteroanterior(PA) oscillatory pressure is applied, through the thumbs, over the process of the hypomobile vertebra.
This oscillatory mobilization, is performed at a frequency of 2Hz (with metronome control/steps) for 2 minutes and repeated 3 times.
The rest time between each mobilization was 1 minute.
This is a manual therapy technique that consist of applied a sustain pressure over cervical hypomobile symptomatic level and request to patient a pain free movement. For performs it, the therapist placed his thumbs on the articular process of that level. The patient sitting. Then, the subject had to perform actively the painful motion while the therapist guides the movement of that vertebra and resists it while returning to neutral. The strength applied was parallel to the plane of the joint, and the procedure was performed in 3 sets of 10 repetitions. |
|
Active Comparator: Mobilisation
This treatment will be applied on cervical spine during four sessions, over two weeks
|
This is a manual therapy technique that consist of applied a sustain pressure over cervical hypomobile symptomatic level and request to patient a pain free movement. For performs it, the therapist placed his thumbs on the articular process of that level. The patient sitting. Then, the subject had to perform actively the painful motion while the therapist guides the movement of that vertebra and resists it while returning to neutral. The strength applied was parallel to the plane of the joint, and the procedure was performed in 3 sets of 10 repetitions.
The Cervical Spine Manipulation is a manual therapy technique directed at the hypomobile and painful vertebral level.
The subject was supine with the cervical spine in a neutral position.
The index finger of the therapist applies contact over the posterolateral aspect of the zygapophyseal joint of the hypomobile vertebra.
The therapist performs the technique taking account the most limited movement; lateral or rotational.
A maximum of 2 attempts will performed on each subject regardless audible cavitation.
|
|
Active Comparator: Mobilization with movement
This Technique will be applied over four sessions, during two weeks
|
The mobilization is a passive oscillatory technique, applied over cervical region in the hypomobile cervical level, the patient will be in prone and the therapist standing at the head of the patients with his thumbs in opposition placed at the level of the facet of the hypomobile cervical vertebra.
A posteroanterior(PA) oscillatory pressure is applied, through the thumbs, over the process of the hypomobile vertebra.
This oscillatory mobilization, is performed at a frequency of 2Hz (with metronome control/steps) for 2 minutes and repeated 3 times.
The rest time between each mobilization was 1 minute.
The Cervical Spine Manipulation is a manual therapy technique directed at the hypomobile and painful vertebral level.
The subject was supine with the cervical spine in a neutral position.
The index finger of the therapist applies contact over the posterolateral aspect of the zygapophyseal joint of the hypomobile vertebra.
The therapist performs the technique taking account the most limited movement; lateral or rotational.
A maximum of 2 attempts will performed on each subject regardless audible cavitation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analogue Scale
Time Frame: The Patients will be followed for 12 weeks after treatment
|
visual analogue scale (VAS).
Despite being a subjective evaluation, it has been documented in previous studies its reliability and validity and its sensitivity to the clinical changes.
For this reason, this scale has been used in numerous clinical trials on neck pains to evaluate the results.
The patient places a vertical mark on a flat horizontal line of 10 cm.
One extreme is 0 (no pain) and the other extreme is 10 (maximum pain) and it must be a difference of 2 points in the evaluation range to produce minimal improvement which is clinically significant.
|
The Patients will be followed for 12 weeks after treatment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neck disability
Time Frame: The Patients will be followed for 12 weeks after treatment
|
The Neck Disability Index (NDI) is an assessment tool used to record the perceived disability in patients with neck pain .It was developed by Howard Vernon from the well-known and validated Oswestry scale for low back pain.
The NDI is a self-administered questionnaire with 10 sections.
7 related to activities of daily living, 2 related to pain and 1 with concentration.
Each of the sections is scored from 0 to 5, and the total score is expressed as a percentage relative to the maximum possible.
The Spanish version was used in this study.
This scale offer a high levels of validity and reliability (infraclass correlation coefficient, ICC: 0.88), is stable against different cultural levels and is consistent and reliable.
The minimum detectable change is 5 points out of 50, while it is recommended t 7 points as the minimum difference clinically important.
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The Patients will be followed for 12 weeks after treatment
|
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Active Cervical Range of Motion
Time Frame: The Patients will be followed for 12 weeks after treatment
|
The ACROM is an instrument that assesses the active range of motion of the cervical segment and has been used in numerous studies to evaluate the results in manual therapy.
Furthermore, it has proven to be a reliable method of measuring, providing a range of intra-meter reliability from 0.7 to 0.9 and a range of inter-meter reliability from 0.8 to 0.87.
It consists of an inclinometers system.
Gravitational inclinometers for flexion-extension and lateral flexion, and magnetic inclinometers for rotation.
The patient, sitting in a chair with the goniometer placed over his head, is asked to perform analytical neck movements (flexion, extension, right lateral flexion, left lateral flexion, right rotation and left rotation) to the point of beginning of pain symptoms or, otherwise, to the fullest extent of mobility.
Each movement is recorded three times to take the average.
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The Patients will be followed for 12 weeks after treatment
|
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Pressure Pain thresholds (PPTs)
Time Frame: pre-treatment and post-treatment
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Pressure pain threshold (PPT) was used in this study for measure the mechanical hyperalgesia.
A digital algometer (FDX 25, Wagner Instruments, Greenwich, CT, USA) comprised of a rubber head (1 cm2) attached to a pressure gauge, was used to measure PPTs.
Force was measured in kilograms/f (kgf).
The measures were taken 3 times at the cervical spine (C2 spinous process), with an interval of 30 seconds between each of the measurements.
An average of the 3 measurements was calculated to obtain a single value for each of the measured points in each of the assessments.
The assessor localized the spinous process of C2.
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pre-treatment and post-treatment
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Satisfaction
Time Frame: The Patients will be followed for 12 weeks after treatment
|
The Global Rating Of Change Scale - GROC is also a commonly used scale in clinical research, particularly in patients with neck pain.
It is designed to quantify the improvements or deterioration over time, and allows the patient to choose the aspects of life that he considers important.
There is variability in the design of the scales, a systematic review in Cochrane quoted seven different designs in the eight studies using a scale of GROC.
This scale goes from -7 (much worse) to +7 (much better) with 0 being the midpoint (equally).
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The Patients will be followed for 12 weeks after treatment
|
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Anxiety
Time Frame: pre-treatment
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All participants completed Spanish version 47 of trait subscale of State Trait Anxiety Inventory (STAI-T.
The STAI-T has been found to possess adequate reliability (alpha coefficients of 0.93, test-retest reliability of 0.80) and validity.
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pre-treatment
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Depression
Time Frame: pre-treatment
|
The level of depressive symptomatology was measured by the Spanish version50 of Beck depression Inventory (BDI-II), a self-report measure which assess affective, cognitive, and somatic symptoms of depression.
The BDI has shown good internal consistency both in original sample (alpha coefficient 0.90) and in Spanish population (alpha coefficient 0.92).
In addition, both versions has an adequate validity
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pre-treatment
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Kinesiophobia
Time Frame: Pre-treatment
|
The Tampa Scale for Kinesiophobia, developed by Miller was used to assess fear of movement and injury.
We used the original 17-items version, which has showed good psychometric guarantees.
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Pre-treatment
|
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Catastrophizing
Time Frame: Pre-Treatment
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To evaluate the subject's propensity to catastrophize about pain we used the Spanish version of Pain Catastrophizing Scale (PCS).
This scale is a 13-item questionnaire designed to measure the three components of catastrophizing: rumination, magnification and helplessness, resulting this evaluation in a unique score
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Pre-Treatment
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Josue Fernandez-Carnero, PhD, Universidad Europea de Madrid/Universidad Rey Juan Carlos
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- A04-12
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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