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Comparison of Two Spinal Manipulation Treatments in Patients With Chronic Mechanical Neck Pain

A Comparative Study Between Cervicothoracic and Upper Cervical Spine Manipulation in Patients With Chronic Mechanical Neck Pain: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04268667
Enrollment
186
Registered
2020-02-13
Start date
2023-02-06
Completion date
2024-03-15
Last updated
2024-03-26

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

Conditions

Neck Pain

Keywords

disability evaluation, musculoskeletal manipulations, neck pain, spinal manipulation

Brief summary

There is enough evidence to suggest that the spinal manipulation of the upper cervical spine and cervicothoracic spine are effective in decreasing neck pain. Therefore, the purpose of this randomized controlled trial is to compare the effects of an isolated application of upper cervical spine thrust joint manipulation with the application of a full combination of cervical, cervico-thoracic and thoracic spine thrust joint manipulation on neck pain, disability and cervical range of motion in individuals with chronic mechanical neck pain.

Interventions

OTHERSpinal manipulation

Application of upper cervical spine thrust joint manipulation or application of a full combination of cervical, cervico-thoracic and thoracic spine thrust joint manipulation.

Sponsors

Clínica Ciudad de Almería
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Symptom persistence for more than 12 weeks. * Age from 18 to 55 years. * Localized pain in the cervical spine. * Symptoms are caused by cervical movement or sustained postures.

Exclusion criteria

* Stage acute of symptoms. * Any contraindication to cervical spinal manipulation (fracture, osteoporosis, joint infections or vertebrobasilar insufficiency). * Patients with previous neck trauma or cervical spine surgery. * Patients diagnosed with cervical radiculopathy. * Patients diagnosed with fibromyalgia. * Have been treated with manual therapy in the last 3 months. * Receiving other treatment during the course of the study.

Design outcomes

Primary

MeasureTime frameDescription
Change in neck pain at rest: Numeric Pain Rating Scale (0-10)Baseline and 7 days post-treatmentNeck pain at rest. Measured with the Numeric Pain Rating Scale (0 = ''no pain'' and 10 = ''worst imaginable pain).
Change in neck disability: Neck Disability Index (0-50)Baseline and 7 days post-treatmentNeck disability is measured with Neck Disability Index (10 items). A higher score indicates greater disability.

Secondary

MeasureTime frameDescription
Change in rigth lateral flexion movement: Cervical Range of Motion deviceBaseline and 7 days post-treatmentRange of cervical motion in right lateral flexion. Measured with a Cervical Range of Motion (CROM) device
Change in left lateral flexion movement: Cervical Range of Motion deviceBaseline and 7 days post-treatmentRange of cervical motion in left lateral flexion. Measured with a Cervical Range of Motion (CROM) device
Change in flexion movement: Cervical Range of Motion deviceBaseline and 7 days post-treatmentRange of cervical motion in flexion. Measured with a Cervical Range of Motion (CROM) device
Change in left rotation movement: Cervical Range of Motion deviceBaseline and 7 days post-treatmentRange of cervical motion in left rotation. Measured with a Cervical Range of Motion (CROM) device
Change in right rotation movement: Cervical Range of Motion deviceBaseline and 7 days post-treatmentRange of cervical motion in right rotation. Measured with a Cervical Range of Motion (CROM) device
Change in extension movement: Cervical Range of Motion deviceBaseline and 7 days post-treatmentRange of cervical motion in extension. Measured with a Cervical Range of Motion (CROM) device

Countries

Spain

Outcome results

None listed

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