- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07034144
- Original Trial
Chiropractic Care for Neck Pain: Comparing Diversified Technique and Drop Table Method (CDTDTM)
Comparison of Chiropractic Diversified Technique and Drop Table Application in Patients With Neck Pain
Study Overview
Status
Intervention / Treatment
Detailed Description
This randomized controlled trial aims to compare the effectiveness of two chiropractic techniques - the Diversified Technique and the Drop Table Technique - in individuals with mechanical neck pain. Mechanical neck pain is a common musculoskeletal condition associated with impaired cervical mobility, pain, and reduced quality of life.
Participants will be randomly assigned to one of three arms: (1) Diversified Technique group, (2) Drop Table Technique group, and (3) control group with no intervention. The interventions will be administered twice per week for four weeks by a chiropractor following standardized protocols. All participants will undergo evaluations at baseline and at the end of the 4-week intervention period.
The primary outcome measure is pain intensity and quality, assessed using the full version of the McGill Pain Questionnaire (MPQ), which evaluates sensory, affective, and evaluative components of pain. Secondary outcomes include cervical range of motion (CROM) and isometric neck muscle strength, measured with a goniometer and handheld dynamometer, respectively.
This study seeks to provide evidence on the comparative clinical effectiveness of two widely used chiropractic techniques for neck pain management. The findings may guide clinicians in selecting appropriate manual therapy approaches for patients with non-specific mechanical neck pain.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: SEFA H HATIK, Asst. Prof.
- Phone Number: +905058761553
- Email: haktanhtk@gmail.com
Study Contact Backup
- Name: OMER D KIZIL, PhD.
- Phone Number: +905415233691
- Email: omerdiclekizil@gmail.com
Study Locations
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-
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Sinop, Turkey
- Sinop University
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Contact:
- SEFA H HATIK, Asst. Prof.
- Phone Number: 905058761553
- Email: haktanhtk@gmail.com
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Principal Investigator:
- SEFA H HATIK, Asst. Prof.
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Sign a voluntary informed consent form.
- Be between 18 and 65 years of age.
- Have previously consulted an orthopedist or physical therapist for neck pain.
- Have no contraindications to chiropractic interventions.
- Have no history of cervical surgery.
- Report neck pain lasting longer than 7 days.
Exclusion Criteria:
- Are under 18 or over 65 years of age.
- Have experienced cervical trauma within the last month.
- Have any systemic illness.
- Have any contraindication for chiropractic intervention (e.g., brain tumor, cervical fracture).
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 |
|---|---|
|
No Intervention: Control Group
This group did not undergo any interventions.
|
|
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Experimental: Diversified Group
Participants in this group will receive chiropractic treatment using the Diversified Technique. The intervention will be applied twice per week for 4 weeks by a chiropractor. The treatment will focus on cervical spine adjustments targeting areas of joint dysfunction associated with mechanical neck pain. Each session will last approximately 20 minutes. Standardized protocols will be followed to ensure consistency. |
Cervical spinal manipulation (SM) will be applied with the participant supine to restrictions found on motion palpation, following the technique described by Bergmann and Peterson. The participant's head and neck will be simultaneously rotated and laterally flexed over the contact point-specifically, the posterior supramastoid groove or zygomatic arch (C0-C1), the posterior aspect of the transverse process (C1-C2), or the posterior articular pillar of superior vertebrae (C2-C7)-to the end of passive range of motion (ROM). Subsequently, a high-velocity, low-amplitude thrust will be delivered in the direction of restricted movement. Participants with greater ROM restriction in the lateral plane will receive more laterally-to-medially directed thrusts. Participants with more restriction in rotation will be given thrusts in the direction of restricted axial rotation, and those with more restriction in extension will receive more anteriorly directed thrusts. |
|
Experimental: Drop Table Group
Participants in this group will receive chiropractic treatment using the Drop Table Technique. The intervention will be applied twice per week for 4 weeks by a chiropractor. The treatment will involve high-velocity, low-amplitude thrusts delivered with the assistance of a segmented drop table designed to reduce resistance and enhance precision during spinal adjustments. The focus will be on the cervical spine region related to mechanical neck pain. Each session will last approximately 20 minutes, following standardized protocols to ensure treatment consistency. |
The Drop Table Technique is a chiropractic intervention that utilizes a segmented treatment table with adjustable sections that can be elevated slightly and then dropped. During the procedure, a high-velocity, low-amplitude (HVLA) thrust is applied while the specific segment of the table drops slightly in coordination with the thrust. This technique aims to reduce the resistance experienced during the adjustment and to enhance the mechanical effect on targeted spinal joints. In this study, the Drop Table Technique will be specifically applied to the cervical spine to address mechanical neck pain. All applications will be performed by a licensed chiropractor using standardized positioning and adjustment protocols to ensure consistency across sessions. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
McGill Pain Questionnaire (MPQ)
Time Frame: Baseline and Week 4
|
Pain will be assessed using the full version of the McGill Pain Questionnaire (MPQ), which evaluates both the sensory, affective, evaluative, and miscellaneous components of pain. The MPQ includes: A list of 78 pain descriptors grouped into 20 categories, The Pain Rating Index (PRI), derived from the sum of rank values for selected descriptors, A Present Pain Intensity (PPI) score, rated on a scale of 0 (no pain) to 5 (excruciating), A Visual Analog Scale (VAS) for overall pain intensity. The primary outcome will be the change in total PRI and PPI scores from baseline to the end of the 4-week intervention. Measure Type: Ordinal and Continuous (PRI: rank-based score; PPI: 0-5 scale) Unit of Measure: Score (no unit) |
Baseline and Week 4
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cervical Range of Motion
Time Frame: Baseline and 4th week
|
Measured in degrees using a goniometer in all planes of cervical motion.
|
Baseline and 4th week
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Isometric Neck Muscle Strength
Time Frame: Baseline and 4th week
|
Isometric neck muscle strength in flexion, extension, and right and left lateral flexion will be manually assessed using a microFET2 handheld dynamometer (Hoggan Health Industries).
|
Baseline and 4th week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: SEFA H HATIK, Asst. Prof., Sinop University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CMT0007
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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