Thrust Manipulation vs. Non-thrust Mobilizations for Mechanical Neck Pain
Primary Purpose
Neck Pain
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Home Exercise Program
Patient advice, encouragement, and education
Thrust Manipulation
Non-thrust Mobilizations
Sponsored by
About this trial
This is an interventional treatment trial for Neck Pain
Eligibility Criteria
Inclusion Criteria:
- Chief complaint of neck pain. (Non-specific neck pain with a primary location between the superior nuchal line and the first thoracic spinous process)
- Age >18
- A minimum Neck Disability Index (NDI) score ≥ 20%
Exclusion Criteria:
- Contraindications to OMT including; malignancy, myelopathy, fracture, metabolic disease, rheumatoid arthritis, long-term corticosteroid use.
Nerve root compression diagnosed as having at least 2 of the following:
- Upper extremity muscle weakness within a specific cervical/thoracic myotome
- Diminished deep tendon reflexes of the biceps brachii, brachioradialis, or triceps muscle.
- Diminished sensation to light touch or pinprick in a specific upper extremity dermatome.
- History of neck or thoracic spine surgery
- Neck pain of <2 on the NPRS
- Currently receiving other forms of conservative care and unwilling to stop for the duration of their participation in the study.
- Any pending litigation related to their neck pain
- Therapist is unable to elicit the chief complaint with passive accessory intervertebral movements (PAIVM).
Sites / Locations
- Youngstown state universityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Thrust Manipulation
Non-thrust Mobilizations
Arm Description
Subjects in this arm will receive spinal thrust manipulation to both the cervical and thoracic spines.
Subjects in this arm will receive spinal non-thrust mobilizations to both the cervical and thoracic spines
Outcomes
Primary Outcome Measures
Change from baseline on the Neck Disability Index (NDI)
The NDI is a self-report measure of perceived disability and it is comprised of ten questions using an ordinal scale from 0 to 5 for a maximum of 50 points. The score is doubled to achieve a % score. The higher an individual scores on the NDI, the greater their perceived level of disability.
Secondary Outcome Measures
Change from baseline on The Patient Specific Functional Scale (PSFS)
The PSFS is a patient identified self-report questionnaire that measures general activity limitations. The scale ranges from 0 (unable to perform) to 10 (able to perform the activity at the level prior to injury). The patient reports three activities that are limited due to the current injury and an average rating for all three activities is calculated.
Change from baseline on The Numerical Pain Rating Scale (NPRS)
The NPRS is an 11-point scale ranging from 0 (no pain) to 10 (worst imaginable pain). Two separate pain ratings will be collected (current and average over a 24 hour period) experienced over 24 hours and then averaged for a composite score.
Change from baseline on The Global Rating Of Change Scale (GROC)
The GROC is a 15-point scale used to quantify a patient's improvement with treatment or to record the clinical course of a condition over time. Patients are asked to describe their overall condition since the start of treatment until the present time with options ranging from -7 ("a very great deal worse") to +7 ("a very great deal better") and 0 being described as "about the same."
Change from baseline on the Deep Cervical Flexion Endurance (DCF)
Patients are positioned in supine and will be instructed to maximally tuck his/her chin isometrically. Patients will then be instructed to lift their head 2.5 cm off the plinth and to maintain upper cervical flexion simultaneously for as long as they were able. A skin fold along the antero-lateral neck will be monitored and the investigator's hand will remain under the occiput of the patient for tactile cueing. The timing of the position began once the patient is in the correct position and stopped if; the patient's head drops into the fingers of the clinician, is elevated greater than one inch, the patient loses the skin fold on the antero-lateral neck, or the patient is unable to continue.
Full Information
NCT ID
NCT02619500
First Posted
November 24, 2015
Last Updated
February 11, 2016
Sponsor
Youngstown State University
Collaborators
Nova Southeastern University
1. Study Identification
Unique Protocol Identification Number
NCT02619500
Brief Title
Thrust Manipulation vs. Non-thrust Mobilizations for Mechanical Neck Pain
Official Title
A Pragmatically Applied Cervical and Thoracic Non-thrust Mobilizations Versus Thrust Manipulation for Patients With Mechanical Neck Pain: A Multicenter Randomized Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
February 2016
Overall Recruitment Status
Unknown status
Study Start Date
February 2016 (undefined)
Primary Completion Date
November 2017 (Anticipated)
Study Completion Date
November 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Youngstown State University
Collaborators
Nova Southeastern University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this clinical trial is to compare the use of thrust manipulation to non-thrust mobilizations for mechanical neck pain when they are applied to both the cervical and thoracic spine. Both of these techniques have been compared in previous trials but a pragmatic approach will be employed as well as controlling for clinical equipoise.
Detailed Description
A total sample size of 136 subjects with mechanical neck pain will be recruited to participant in this trial from multiple clinic and university sites around the country. Each subject will be evaluated by a licensed physical therapist that specializes in orthopedic manual therapy (OMT). Each treating therapist will be blinded be the data collection and each data collection therapist will be blinded to the treatment allocation. Subjects data will be collected at the initial visit, second visit, and at discharge. The maximum number of weeks that a subject may be enrolled is 8 weeks (2 months). At that point, they are discharged from the study. The treating therapist will allocate the subject through the already completed randomization procedures. Once the subject is randomized, the treating therapist will perform the OMT based on their clinical reasoning and in a manner they feel would benefit the patient the most. In addition to the OMT, each subject will receive a home exercise program, advice, encouragement, and education. A number of outcome variables will be collected regarded pain and disability as well as one physical performance measure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neck Pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
136 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Thrust Manipulation
Arm Type
Experimental
Arm Description
Subjects in this arm will receive spinal thrust manipulation to both the cervical and thoracic spines.
Arm Title
Non-thrust Mobilizations
Arm Type
Active Comparator
Arm Description
Subjects in this arm will receive spinal non-thrust mobilizations to both the cervical and thoracic spines
Intervention Type
Other
Intervention Name(s)
Home Exercise Program
Intervention Description
A standardized home exercise program will be given to subjects that will include active range of motion of the cervical and thoracic spine and deep cervical flexion endurance exercises.
Intervention Type
Other
Intervention Name(s)
Patient advice, encouragement, and education
Intervention Description
Therapists will provide each subject with advice and education pertaining to their condition as well as encouragement towards reducing pain and disability.
Intervention Type
Other
Intervention Name(s)
Thrust Manipulation
Intervention Description
High velocity low amplitude (HVLA) thrust performed at or near the end range of a targeted segment in both the cervical and thoracic spine
Intervention Type
Other
Intervention Name(s)
Non-thrust Mobilizations
Intervention Description
Repetitive and rhythmic accessory passive movements applied with either small or large amplitude at a targeted segment to both the cervical and thoracic spine
Primary Outcome Measure Information:
Title
Change from baseline on the Neck Disability Index (NDI)
Description
The NDI is a self-report measure of perceived disability and it is comprised of ten questions using an ordinal scale from 0 to 5 for a maximum of 50 points. The score is doubled to achieve a % score. The higher an individual scores on the NDI, the greater their perceived level of disability.
Time Frame
3 days and 8 weeks
Secondary Outcome Measure Information:
Title
Change from baseline on The Patient Specific Functional Scale (PSFS)
Description
The PSFS is a patient identified self-report questionnaire that measures general activity limitations. The scale ranges from 0 (unable to perform) to 10 (able to perform the activity at the level prior to injury). The patient reports three activities that are limited due to the current injury and an average rating for all three activities is calculated.
Time Frame
3 days and 8 weeks
Title
Change from baseline on The Numerical Pain Rating Scale (NPRS)
Description
The NPRS is an 11-point scale ranging from 0 (no pain) to 10 (worst imaginable pain). Two separate pain ratings will be collected (current and average over a 24 hour period) experienced over 24 hours and then averaged for a composite score.
Time Frame
3 days and 8 weeks
Title
Change from baseline on The Global Rating Of Change Scale (GROC)
Description
The GROC is a 15-point scale used to quantify a patient's improvement with treatment or to record the clinical course of a condition over time. Patients are asked to describe their overall condition since the start of treatment until the present time with options ranging from -7 ("a very great deal worse") to +7 ("a very great deal better") and 0 being described as "about the same."
Time Frame
3 days and 8 weeks
Title
Change from baseline on the Deep Cervical Flexion Endurance (DCF)
Description
Patients are positioned in supine and will be instructed to maximally tuck his/her chin isometrically. Patients will then be instructed to lift their head 2.5 cm off the plinth and to maintain upper cervical flexion simultaneously for as long as they were able. A skin fold along the antero-lateral neck will be monitored and the investigator's hand will remain under the occiput of the patient for tactile cueing. The timing of the position began once the patient is in the correct position and stopped if; the patient's head drops into the fingers of the clinician, is elevated greater than one inch, the patient loses the skin fold on the antero-lateral neck, or the patient is unable to continue.
Time Frame
3 days and 8 weeks
Other Pre-specified Outcome Measures:
Title
Questionnaire using a scale that rates each clinicians own Clinical Equipoise
Description
Therapist equipoise will be measured globally regarding both of the orthopedic manual therapy techniques on a single scale that ranges form 0 to +2 (only a single measure. Each treating therapist will make a global opinion regarding the efficacy of non-thrust mobilization compared to thrust manipulation. An ordinal scale will be used with a score of 0 meaning that the clinician does not believe that either of the competing treatments are more beneficial than the other. The scale then ranges from +1 and +2 for both mobilizations and manipulations. The rater circles if one of the numbers depending on which of the treatments they feel are clinically more effective. See below.
Mobilization is better Neither Manipulation is better
+2 - 1 - 0 - +1 - +2
Time Frame
baseline only
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Chief complaint of neck pain. (Non-specific neck pain with a primary location between the superior nuchal line and the first thoracic spinous process)
Age >18
A minimum Neck Disability Index (NDI) score ≥ 20%
Exclusion Criteria:
Contraindications to OMT including; malignancy, myelopathy, fracture, metabolic disease, rheumatoid arthritis, long-term corticosteroid use.
Nerve root compression diagnosed as having at least 2 of the following:
Upper extremity muscle weakness within a specific cervical/thoracic myotome
Diminished deep tendon reflexes of the biceps brachii, brachioradialis, or triceps muscle.
Diminished sensation to light touch or pinprick in a specific upper extremity dermatome.
History of neck or thoracic spine surgery
Neck pain of <2 on the NPRS
Currently receiving other forms of conservative care and unwilling to stop for the duration of their participation in the study.
Any pending litigation related to their neck pain
Therapist is unable to elicit the chief complaint with passive accessory intervertebral movements (PAIVM).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David W Griswold, DPT
Phone
330-941-2419
Email
dwgriswold@ysu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Ken L Learman, PhD
Phone
330-947125
Email
klearman@ysu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Josh Cleland, PhD
Organizational Affiliation
Nova Southeastern University
Official's Role
Study Chair
Facility Information:
Facility Name
Youngstown state university
City
Youngstown
State/Province
Ohio
ZIP/Postal Code
44406
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David W Griswold, DPT
Phone
330-701-5353
Email
Dwgriswold@ysu.edu
First Name & Middle Initial & Last Name & Degree
Ken L Learman, PhD
Phone
3302617376
Email
Klearman@ysu.edu
12. IPD Sharing Statement
Citations:
PubMed Identifier
26109828
Citation
Griswold D, Learman K, O'Halloran B, Cleland J. A preliminary study comparing the use of cervical/upper thoracic mobilization and manipulation for individuals with mechanical neck pain. J Man Manip Ther. 2015 May;23(2):75-83. doi: 10.1179/2042618614Y.0000000095.
Results Reference
background
PubMed Identifier
25125936
Citation
Young JL, Walker D, Snyder S, Daly K. Thoracic manipulation versus mobilization in patients with mechanical neck pain: a systematic review. J Man Manip Ther. 2014 Aug;22(3):141-53. doi: 10.1179/2042618613Y.0000000043.
Results Reference
background
PubMed Identifier
21979312
Citation
Dunning JR, Cleland JA, Waldrop MA, Arnot CF, Young IA, Turner M, Sigurdsson G. Upper cervical and upper thoracic thrust manipulation versus nonthrust mobilization in patients with mechanical neck pain: a multicenter randomized clinical trial. J Orthop Sports Phys Ther. 2012 Jan;42(1):5-18. doi: 10.2519/jospt.2012.3894. Epub 2011 Sep 30.
Results Reference
background
PubMed Identifier
23040656
Citation
Cook C, Learman K, Showalter C, Kabbaz V, O'Halloran B. Early use of thrust manipulation versus non-thrust manipulation: a randomized clinical trial. Man Ther. 2013 Jun;18(3):191-8. doi: 10.1016/j.math.2012.08.005. Epub 2012 Oct 2.
Results Reference
background
PubMed Identifier
29406835
Citation
Griswold D, Learman K, Kolber MJ, O'Halloran B, Cleland JA. Pragmatically Applied Cervical and Thoracic Nonthrust Manipulation Versus Thrust Manipulation for Patients With Mechanical Neck Pain: A Multicenter Randomized Clinical Trial. J Orthop Sports Phys Ther. 2018 Mar;48(3):137-145. doi: 10.2519/jospt.2018.7738. Epub 2018 Feb 6.
Results Reference
derived
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Thrust Manipulation vs. Non-thrust Mobilizations for Mechanical Neck Pain
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