Effect of First and Second Rib Mobilization in Patients With Non-Specific Neck Pain
NCT ID: NCT06796452
Last Updated: 2025-07-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
44 participants
INTERVENTIONAL
2025-03-01
2025-07-13
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Integrated Neuromuscular Inhibition, Muscle Energy and Strain Counter Strain Techniques in Neck Pain
NCT05262062
Cervicothoracic Junction Mobilization Versus Eccentric Muscle Energy Technique in Mechanical Cervical Pain
NCT05410067
Effects of Kinesiotherapy Exercises With Cervical Mobilization in Cervicobrachial Neuralgia
NCT06459466
Effects of Diaphragm Manual Therapy Verses Sustained Natural Apophyseal Glide in Mechanical Neck Pain
NCT06460532
Effects of Scapular Stabilization Versus Thoracic Spine Extension Exercises in Mechanical Neck Pain
NCT05353088
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Despite the extensive research on non-specific neck pain (NSNP) and various therapeutic interventions, there is a notable gap in the literature regarding the specific effects of first and second rib mobilization on pain, range of motion, muscle endurance, and disability in patients with NSNP. While studies have explored manual therapies, proprioceptive exercises, and virtual reality as complementary interventions, the direct impact of rib mobilization, especially involving both the first and second ribs, remains under-investigated. Additionally, most existing studies focus on short-term outcomes, and there is limited evidence on the long-term effects of rib mobilization techniques.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Ribs Mobilization
will receive Maitland first and second Rib Mobilization with three sets of 6-8 repetitions in each session and conventional(Baseline) Physical therapy Treatment.
Ribs Mobilization
Three sets of 6-8 repetitions in each session and conventional(Baseline) Physical therapy Treatment.
Conventional Treatment
will only receive Baseline Physical therapy treatment
Conventional treatment
* Hot pack for 8 min
* Maitland Generalized Cervical Mobilizations (6-8 REPS,3 sets)
* Isometric Strengthening Exercise
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Ribs Mobilization
Three sets of 6-8 repetitions in each session and conventional(Baseline) Physical therapy Treatment.
Conventional treatment
* Hot pack for 8 min
* Maitland Generalized Cervical Mobilizations (6-8 REPS,3 sets)
* Isometric Strengthening Exercise
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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)
Exclusion Criteria
* Past surgical history of cervical and thoracic region
* Thoracic Outlet syndrome and Cervical radiculopathy
* Congenital anomalies of spine and ribs
20 Years
45 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Riphah International University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Syed Sramad Hussain Bukhari, MSOMPT
Role: PRINCIPAL_INVESTIGATOR
Riphah International University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Murtaza Rehabilitation center
Lahore, Punjab Province, Pakistan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
REC/RCR&AHS/24/0156
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.