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Immediate Effect of a Single Cervical Spinal Manipulation (SMCervical)

Primary Purpose

Neck Pain

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Cervical manipulation intervention
Placebo intervention
Sponsored by
University of Valencia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neck Pain focused on measuring neck pain, manual therapy, movement

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Perceived pain scored 3 or above, in a visual analogue scale
  • Neck functional status revealing a mild disability
  • Minimun duration of the symptoms being one month.

Exclusion Criteria:

  • inflammatory rheumatic disease or an inner ear disorder.
  • the use of antidepressant opioid or sedative drugs.
  • current vertigo or dizziness.
  • visual loss.
  • neurological disorder,
  • trunk or shoulder surgery within the past year.

Sites / Locations

  • Gemma Victoria Espí-López

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Cervical manipulation intervention

Placebo intervention

Arm Description

To perform the evaluation and detect the cervical vertebral level with mobility restriction, with the patient in supine position, a cervical examination is carried out to determine the mobility restriction, both in flexo-extension, as in inclination and rotation. To check the level of restriction, the post-anterior sliding test is performed. The manipulation is performed following the criteria of thrust manipulations. A maximum of 3 manipulations are applied in total per subject, one for each level (high level C1-C2, medium level C3-C6, and low level C7), if necessary.

This group will receive 15 minutes of sham techniques in a supine position over the stretcher. First, a series of short-time and no pressure contact with physiotherapist´s hands is performed in several points of head and shoulders for 10 minutes. Subsequently, light touch is applied on standardized anatomic areas, for 2 minutes each time.

Outcomes

Primary Outcome Measures

Range of motion
Angular excursion of the cervical motion.
Harmonicity
Is the absolute value of the correlation coefficient between: Ӫ and Ө. Thus Harmonicity quantifies the fit between the actual movement and the simple harmonic motion.

Secondary Outcome Measures

Disability of the neck
To determine how neck pain affects a patient's daily life. Scoring is reported on a 0-50 scale, 0 being the best possible score.
Impression of Change
The self-reported measure 'Patient Global Impression of Change' that reflects a patient's belief about the efficacy of treatment. This is a one-item questionnaire in which patients rank their change following an intervention on a scale from 1 to 7 (1, very much improved; 2, much improved; 3, minimally improved; 4, no change; 5, minimally worse; 6, much worse; 7, very much worse).

Full Information

First Posted
August 14, 2019
Last Updated
April 16, 2020
Sponsor
University of Valencia
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1. Study Identification

Unique Protocol Identification Number
NCT04059692
Brief Title
Immediate Effect of a Single Cervical Spinal Manipulation
Acronym
SMCervical
Official Title
Immediate Effect of a Single Cervical Spinal Manipulation on Cervical Movement Pattern
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
December 15, 2019 (Actual)
Study Completion Date
December 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Valencia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Objective: The aim of the present study is to analyze the immediate effect of a single cervical spinal manipulation on cervical movement pattern. Further, To perform the sample size calculation, the investigators took into consideration that the investigators pretend to achieve a medium effect size (d=0.5) of the differences with two groups (EG and CG) and two aimed to explore the impact on pain, disability and patient's improvement-perceived sensation, comparing with a placebo. Methods: The study design is experimental and purposive sampling was used to select the study participants. The grouping allocation was randomized. The people volunteer to participate in the study, are assigned to the experimental group (EG) that will receive a single manipulation, to the control group (CG) that will receive a single placebo treatment. The participants will be assessed twice, one before the treatment and the other, after the end. Head movement is recorded by means of a video-photogrammetry system from the coordinates of a set of eight reflective markers located on a helmet. The movements will be record at 200 fps. In each evaluation, the perceived pain and the neck disability index are also recorded. And the impression of change is evaluated only in the second evaluation. Outcomes. Pain, Disability of the neck, Impression of Change, Range of motion (RoM), Maximum angular velocity (MAV), Maximum angular acceleration (MAA) and Harmonicity (HARM). Intervention: The intervention, in both groups, it includes only one session that lasted 15 minutes approximately: a) Cervical manipulation intervention and b)Placebo intervention.
Detailed Description
INTRODUCTION Non-specific neck pain is defined as pain in the posterior and lateral aspect of the neck between the superior nuchal line and the spinous process of the first thoracic vertebra with no signs or symptoms of major structural pathology. It is a common musculoskeletal disorder that leads to substantial disability, discomfort, and reduced cervical mobility, resulting in enormous health costs in terms of treatment and work absenteeism. The American Physical Therapy Association's guidelines on neck pain recommends utilizing cervical manipulation (CM) and mobilization procedures to reduce neck pain based on strong evidence. Spinal manipulation is defined as "a passive, high velocity, low amplitude thrust applied to a joint complex within its anatomical limit with the intent to restore optimal motion, function, and/or to reduce pain" and its effectiveness, concretely of a continuous program of cervical manipulations (CM), on neck pain has been largely studied. A previous systematic review concluded that treatments based on CM are effective both alone and in combination with exercises whilst other systematic reviews and an evidence-based guideline showed that CM, combined with exercises, resulted to be more effective for neck pain, function, and global perceived effect, than a therapeutic program based, exclusively, on CM. Nevertheless, the underlying mechanisms of the pain decrease with this therapeutic approach are not completely understood. A recent study aimed at analyzing the biomechanics of a single CM, used a complex system of synchronized biplane radiographs to measure the facet gapping during a single manipulation. Authors demonstrated that target and adjacent motion segments undergo facet joint gapping during a manipulation and that segmental and global range of motion (ROM) increases in all three planes of motion immediately after one manipulation. In the clinical setting, the best of our knowledge, only one previous clinical trial have analyzed the effectiveness of a single cervical manipulation on cervical range of motion, comparing with placebo, demonstrating an improvement in all the global maximum cervical movements, measured with the goniometer. However, pain may affect other movement' characteristics beside the maximum range of motion (ROM), as velocity, variability or movement harmony. Nevertheless, no previous study has analyzed the characteristics of the patients' cervical motion pattern after a single manipulation which could provide information about functional changes in cervical movements. People with neck pain, has shown more slow movements, less harmonic movements in the points close to pain and exponential trend at the ends of the range, even when cervical spine motion ranges remain within normal limits. The investigators hypothesized that functional assessment of the cervical spine based on the analysis of the motion pattern, will let us know if a single manipulation is effective in the improvement of those variables. The aim of the present study is to analyze the immediate effect of a single cervical spinal manipulation on cervical movement pattern. Further, the investigators aimed to explore the impact on pain, disability and patient's improvement-perceived sensation, comparing with a placebo. METHODS Participants The study design is experimental and purposive sampling was used to select the study participants. The grouping allocation was randomized. The people volunteer to participate in the study, are assigned to the experimental group (EG) that will receive a single CM, to the control group (CG) that will receive a single placebo treatment. All the participants should meet the following inclusion criteria: perceived pain scored 3 or above, in a visual analogue scale, and neck functional status revealing a mild disability. Additionally, patients had symptoms duration less than 30 days. For both groups, the exclusion criteria include an inflammatory rheumatic disease or an inner ear disorder, the use of antidepressant opioid or sedative drugs, current vertigo or dizziness, visual loss, neurological disorder, and trunk or shoulder surgery within the past year. Sample size To perform the sample size calculation, the investigators took into consideration to achieve a medium effect size (d=0.5) of the differences with two groups (EG and CG) and two assessments (pre and post-treatment). Further, the investigators set a type I error of 5%, and a type II error of 20%. This power calculation resulted in 17 patients on each group. Assessment procedures The participants will be assessed twice, one before the treatment and the other, after the end. Head movement is recorded by means of a video-photogrammetry system from the coordinates of a set of eight reflective markers located on a helmet. The movements will be record at 200 fps. Participants sit in a chair with the trunk fixed at the back by means of belts. In each session, they perform three movements: flexion-extension (FE), lateral flexion (LB) and axial rotation (AR) whose order was randomized. Each movement will be perform seven consecutive times without stopping and achieving a continuous and smooth cyclic movement with the maximum achievable range at their preferred speed. The participants are encouraged to practice the three movements before the test begins, to avoid the learning effect. In each evaluation, the perceived pain and the neck disability index are also recorded. And the impression of change is evaluated only in the second evaluation. Outcomes Pain, with the Visual Analogue Scale (VAS), in which the patients marked their level of pain intensity on a 10-cm horizontal line (0= no pain to 10= maximum pain) at the time the assessment was carried out. Disability of the neck, with the 'Neck Disability Index', a self-report questionnaire used to determine how neck pain affects a patient's daily life. Scoring is reported on a 0-50 scale, 0 being the best possible score. Impression of Change, with the self-reported measure 'Patient Global Impression of Change' that reflects a patient's belief about the efficacy of treatment. Range of motion (RoM): angular excursion of the cervical motion. Maximum angular velocity(MAV), it is measured as percentile 95 of angular velocity during the test. Maximum angular acceleration(MAA), it is measas percentile 95 of angular acceleration during the test. Harmonicity (HARM): is the absolute value of the correlation coefficient between two motion. Thus HARM quantifies the fit between the actual movement and the simple harmonic motion. Intervention The intervention, in both groups, it includes only one session that lasted 15 minutes approximately. Participants should wear a sleeveless shirt that allows the physiotherapist to treat the neck region. Evaluations and manipulations are performed by the same experienced physiotherapist. Cervical manipulation intervention Prior to intervention, a screened for any signs of vertebrobasilar insufficiency is performed by means of the vertebral artery compromise test, as well as the root compression test using the Jackson test, and the screening for upper cervical spine ligamentous instability through Sharp-Purser test, alar ligament stress test and transverse ligament test. To perform the evaluation and detect the cervical vertebral level with mobility restriction, with the patient in supine position, a cervical examination is carried out to determine the mobility restriction, both in flexo-extension, as in inclination and rotation. To check the level of restriction, the post-anterior sliding test is performed. Once the vertebral levels with restriction have been detected, high speed and low amplitude manipulation is carried out based on the location of the pain and the detection of the perceived joint hypomobility, using the clinical criterion for this, with a maximum of 2 manipulative attempts by vertebral level, regardless of having achieved joint cavitation. The manipulation is performed following the criteria of thrust manipulations. A maximum of 3 manipulations are applied in total per subject, one for each level (high level C1-C2, medium level C3-C6, and low level C7), if necessary. Placebo intervention This group will receive 15 minutes of sham techniques in a supine position over the stretcher. First, a series of short-time and no pressure contact with physiotherapist´s hands is performed in several points of head and shoulders for 10 minutes. Subsequently, light touch is applied on standardized anatomic areas, equal to those treated with manipulative intervention, for 2 minutes each time, adding a total duration of approximately 15 minutes, similar to the intervention group. Statistics Standard statistical methods will be use to obtain the mean and standard deviation of the mean (SD). For the inferential analysis of the data, a mixed two-factor multivariate analysis of variance (MANOVA) with a between-subject factor 'group' (i.e. CG and EG) ant a within-subject factor 'time' with two groups (pre and post-intervention). Multiple comparison techniques are performed using Bonferroni correction. The investigators will evaluate the assumption of homoscedasticity and it will be assumed in each variable. In addition, the investigators will compare the perceived changes after treatment between the two groups with an independent Student T test. Type I error will be set as <5% (p <.05).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neck Pain
Keywords
neck pain, manual therapy, movement

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study design is experimental
Masking
ParticipantOutcomes Assessor
Masking Description
The subjects do not know the group to which they belong. The evaluator does not know the treatment applied.
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cervical manipulation intervention
Arm Type
Experimental
Arm Description
To perform the evaluation and detect the cervical vertebral level with mobility restriction, with the patient in supine position, a cervical examination is carried out to determine the mobility restriction, both in flexo-extension, as in inclination and rotation. To check the level of restriction, the post-anterior sliding test is performed. The manipulation is performed following the criteria of thrust manipulations. A maximum of 3 manipulations are applied in total per subject, one for each level (high level C1-C2, medium level C3-C6, and low level C7), if necessary.
Arm Title
Placebo intervention
Arm Type
Placebo Comparator
Arm Description
This group will receive 15 minutes of sham techniques in a supine position over the stretcher. First, a series of short-time and no pressure contact with physiotherapist´s hands is performed in several points of head and shoulders for 10 minutes. Subsequently, light touch is applied on standardized anatomic areas, for 2 minutes each time.
Intervention Type
Other
Intervention Name(s)
Cervical manipulation intervention
Intervention Description
Cervical manipulative technique
Intervention Type
Other
Intervention Name(s)
Placebo intervention
Intervention Description
Sham intervention
Primary Outcome Measure Information:
Title
Range of motion
Description
Angular excursion of the cervical motion.
Time Frame
1 day
Title
Harmonicity
Description
Is the absolute value of the correlation coefficient between: Ӫ and Ө. Thus Harmonicity quantifies the fit between the actual movement and the simple harmonic motion.
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Disability of the neck
Description
To determine how neck pain affects a patient's daily life. Scoring is reported on a 0-50 scale, 0 being the best possible score.
Time Frame
1 day
Title
Impression of Change
Description
The self-reported measure 'Patient Global Impression of Change' that reflects a patient's belief about the efficacy of treatment. This is a one-item questionnaire in which patients rank their change following an intervention on a scale from 1 to 7 (1, very much improved; 2, much improved; 3, minimally improved; 4, no change; 5, minimally worse; 6, much worse; 7, very much worse).
Time Frame
1 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Perceived pain scored 3 or above, in a visual analogue scale Neck functional status revealing a mild disability Minimun duration of the symptoms being one month. Exclusion Criteria: inflammatory rheumatic disease or an inner ear disorder. the use of antidepressant opioid or sedative drugs. current vertigo or dizziness. visual loss. neurological disorder, trunk or shoulder surgery within the past year.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gemma V Espí-López
Organizational Affiliation
Faculty of Physiotherapy. University of Valencia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gemma Victoria Espí-López
City
Valencia
ZIP/Postal Code
46010
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
20534314
Citation
Rey-Eiriz G, Alburquerque-Sendin F, Barrera-Mellado I, Martin-Vallejo FJ, Fernandez-de-las-Penas C. Validity of the posterior-anterior middle cervical spine gliding test for the examination of intervertebral joint hypomobility in mechanical neck pain. J Manipulative Physiol Ther. 2010 May;33(4):279-85. doi: 10.1016/j.jmpt.2010.03.005.
Results Reference
result
PubMed Identifier
21335931
Citation
Puentedura EJ, Landers MR, Cleland JA, Mintken PE, Huijbregts P, Fernandez-de-Las-Penas C. Thoracic spine thrust manipulation versus cervical spine thrust manipulation in patients with acute neck pain: a randomized clinical trial. J Orthop Sports Phys Ther. 2011 Apr;41(4):208-20. doi: 10.2519/jospt.2011.3640. Epub 2011 Feb 18.
Results Reference
result

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Immediate Effect of a Single Cervical Spinal Manipulation

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