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The Effect of the Bridge Technique Mobilization With Movement Versus Trapezius Dry Needling in the Management of Cervical Dysfunction

The Effect of the Bridge Technique Mobilization With Movement Versus Trapezius Dry Needling in the Management of Cervical Dysfunction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07134062
Enrollment
40
Registered
2025-08-21
Start date
2020-05-01
Completion date
2020-12-01
Last updated
2025-08-21

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

Conditions

Dry Needling Technique, Mulligan Mobilization, Physical Therapy

Brief summary

This study investigates the effect of the Bridge technique mobilization with movement compared to the Trapezius Dry Needling technique on physiotherapy outcome in patients with cervical dysfunction.

Interventions

OTHERBridge technique MWM

Patient in supine, head resting on a pillow, cervical spine relaxed in a neutral position, physiotherapist sitting or standing at the head of the table. Hands support both sides of the head through the thenar eminence on each side, fingers in contact with the C7, T1or T2 articular pillar bilaterally.

OTHERDry Needling

Participants in this group received two sessions per week of D.N. treatment for the trapezius muscle.

Sponsors

Al-Quds University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Adult patients aged (25 - 65) years, males & females. * Cervical dysfunction * Orthopedic dysfunction without neurological defects * Limitation in ROM (extension & rotation) * VAS scale scores for neck pain must be \> 4/10 * Neck pain aggravated by neck posture or movement * Willing to give an informed consent

Exclusion criteria

* Any known medical condition, cardio, cancer * Manipulative treatment within the past three months * Previous spinal surgery in the past five years * Current use of medication * Disc prolapse acute stage * previous epidural injection since the onset of present symptoms * diagnosis of any generalized neurological disorder * medical red flags suggestive of severe pathology * pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Numeric Visual analogue scale (VAS)pre and 1 day post treatmentIs the most commonly used method for assessing pain intensity. The leftmost value on the 10-cm horizontal line used for VAS indicates a painless condition represented by 0. The rightmost value is 10, which represents extreme pain. The subjects rated their feelings of pain on the line by themselves, thereby quantifying the pain. The validity and reliability are very high.
Quality of life Questionnaire (QoL)pre and 1 day post treatmentIs an instrument for measuring the Quality of an individual's life across a broad range of specific areas. Quality of life (QoL) could be viewed as a subjective, multidimensional concept that emphasizes an individual's current state's self-perception. However, the general Quality of life includes individuals' evaluation of all aspects of life, including the safety of the environment in which they live, whether they feel they have access to health care and social services, and their current spiritual status
The Northwick Park Neck Pain Questionnaire (NPQ)pre and 1 day post treatmentMeasures neck pain and consequent patient disabilities. It is easy to complete, to score, and it gives an objective measure to assess the monitor symptoms and outcome in patients with acute or chronic neck pain over time.
Neck Disability Index (NDI)pre and 1 day post treatmentThe Neck Disability Index (NDI) was grown in (1989) by Howard Vernon. The Index developed to modify the Oswestry Low Back Pain Disability Index with the original author's permission J. Fairbank, (1980). Vernon and Mior at (1991) the reliability and validity analysis finding have been published in the Manipulative and Physiologic Therapeutics Journal.

Countries

Palestinian Territories

Outcome results

None listed

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