Effect of Rib Mobilization and Diaphragm Release Techniques in Patients With Non-Specific Neck Pain
1 other identifier
interventional
100
1 country
1
Brief Summary
Rib mobilization is a therapeutic technique aimed at enhancing the mobility of the ribcage, which can have a significant impact on neck pain, even when the pain is classified as non-specific. The ribcage plays a crucial role in maintaining the alignment and posture of the upper body, including the neck. When the ribs are restricted or misaligned, it can lead to compensatory movements and increased strain on the cervical spine, contributing to neck pain. By mobilizing the ribs, we can restore their natural movement, which in turn can release tension in the surrounding musculature and improve the overall biomechanics of the thoracic and cervical regions. This approach not only addresses the immediate symptoms of neck pain but also targets the underlying structural issues that may perpetuate discomfort.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 14, 2025
CompletedFirst Posted
Study publicly available on registry
August 21, 2025
CompletedStudy Start
First participant enrolled
October 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2025
CompletedDecember 2, 2025
December 1, 2025
2 months
August 14, 2025
December 1, 2025
Conditions
Outcome Measures
Primary Outcomes (2)
Numerical Pain Rating Scale (NPRS)
The Numerical Pain Rating Scale (NPRS) is a subjective measure used to assess the intensity of neck pain in individuals. Patients are asked to rate their pain on a scale from 0 to 10, where 0 represents "no pain" and 10 signifies "the worst possible pain." This simple tool provides a quantitative measure of pain, enabling healthcare providers to evaluate the severity of the patient's condition and monitor changes over time. The NPRS is widely used due to its ease of application and effectiveness in capturing patient-reported pain intensity
at baseline and at 8 weeks
Neck range of motion (ROM)
A goniometer is an instrument used to measure the range of motion (ROM) of the neck. It is an essential tool for evaluating the flexibility and mobility of the cervical spine. During the assessment, the goniometer is aligned with specific anatomical landmarks to measure the angles of neck flexion, extension, lateral flexion, and rotation. This objective data is crucial for identifying limitations in neck movement, which could contribute to pain and functional impairment. The goniometer is considered reliable and valid for assessing cervical ROM in clinical settings
at baseline and at 8 weeks
Secondary Outcomes (2)
Neck flexor Muscle Endurance Test
at baseline and at 8 weeks
Neck Disability Index
at baseline and at 8 weeks
Study Arms (3)
RMT and DRT(Rib Mobilization Technique and Diaphragm Release Technique)
EXPERIMENTALRib Mobilization Technique and Diaphragm Release Technique(In the seated position, the participants remained seated on the stretcher, keeping the feet on the floor, while the therapist stood in front of him or her. The participant's head (frontal region) was positioned over his or her overlapping arms, which were placed on the therapist's trunk )
DRT(Diaphragm Release Technique)
EXPERIMENTALDiaphragm Release Technique:The DRT was performed according to the protocol described by Rocha et al.13 In this protocol, the participant remains in the supine position so that the therapist is able to maintain manual contact with the bottom edge of the rib cage
control
NO INTERVENTIONNo intervention
Interventions
The RMT, adapted from Henderson et al10 and Abdelaal et al,15 was carried out in 2 different participant positions: supine and seated. In the supine position, the therapist was placed next to the participant and positioned the last 4 fingertips of both hands at the rib angles. The therapist mobilized the costal angles in the postero anterior direction accompanying the participant's normal inspiration The movement was performed in 2 series of 10 respiratory cycles in each hemi thorax, with a 1-minute interval between sets.
The DRT was performed according to the protocol described by Rocha et al.13 In this protocol, the participant remains in the supine position so that the therapist is able to maintain manual contact with the bottom edge of the rib cage. During inspiration, the therapist exerts traction after the natural rib-cage movement, then deepens the manual contact and maintains the resistance exerted in the previous phase throughout exhalation. The technique was applied in 2 series of 10 deep respiratory cycles, with a 1-minute interval between the series, under the therapist's verbal command.
Eligibility Criteria
You may qualify if:
- Neurological tests will be negative
- Both genders having age between 20 to 45 years
- Participants should have primary complaint of neck pain
- Neck Disability Index (NDI) score of 20% or greater (i.e. 10 points or greater on a 0 to 50 scale)
- A pain intensity of ≥4 on the 10-point Numerical Pain Rating Scale (NPRS)
You may not qualify if:
- First and second rib fracture and dislocation
- Past surgical history of cervical and thoracic region
- Thoracic Outlet syndrome and cervical radiculopathy
- Congenital anomalies of spine and ribs
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- MTI Universitylead
Study Sites (1)
faculty of physical therapy ,Cairo University
Cairo, 11311, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assisstant professor
Study Record Dates
First Submitted
August 14, 2025
First Posted
August 21, 2025
Study Start
October 1, 2025
Primary Completion
December 1, 2025
Study Completion
December 1, 2025
Last Updated
December 2, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share