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Chiropractic Care for Neck Pain: Comparing Diversified Technique and Drop Table Method

Comparison of Chiropractic Diversified Technique and Drop Table Application in Patients With Neck Pain

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07034144
Acronym
CDTDTM
Enrollment
45
Registered
2025-06-24
Start date
2025-06-14
Completion date
2025-08-14
Last updated
2025-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Manipulation, Neck Pain, Non Specific Neck Pain, Chiropractic

Keywords

Chiropractic, Neck pain, Drop Table, Spinal Manipulation

Brief summary

This study aims to compare the effects of two different chiropractic techniques, Diversified and Drop Table, on pain levels, cervical joint range of motion, and neck muscle strength in individuals with non-specific neck pain.

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.

Interventions

OTHERDrop Table Technique

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.

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.

Sponsors

SEFA HAKTAN HATIK
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

This study is designed as a double-blind, randomized controlled trial involving three groups: the Diversified technique group, the Drop Table application group, and a control group. Although the nature of manual therapy prevents complete blinding of participants, all were only informed that they would receive chiropractic care, without specifying the technique applied. Thus, participants were blinded to the specific intervention type. The practitioners administering the treatments were not blinded due to the need to apply the appropriate technique. However, all outcome assessments were performed by an independent evaluator who was blinded to group allocation and not involved in the intervention process, ensuring objective measurement.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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).

Design outcomes

Primary

MeasureTime frameDescription
McGill Pain Questionnaire (MPQ)Baseline and Week 4Pain 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)

Secondary

MeasureTime frameDescription
Cervical Range of MotionBaseline and 4th weekMeasured in degrees using a goniometer in all planes of cervical motion.
Isometric Neck Muscle StrengthBaseline and 4th weekIsometric neck muscle strength in flexion, extension, and right and left lateral flexion will be manually assessed using a microFET2 handheld dynamometer (Hoggan Health Industries).

Countries

Turkey (Türkiye)

Contacts

Primary ContactSEFA H HATIK, Asst. Prof.
haktanhtk@gmail.com+905058761553
Backup ContactÖMER D KIZIL, PhD.
omerdiclekizil@gmail.com+905415233691

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026