Effects of Neural Mobilization on Respiratory Parameters in Chronic Neck Pain
NCT ID: NCT05867082
Last Updated: 2024-08-01
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
26 participants
INTERVENTIONAL
2023-06-26
2023-10-27
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Methods: Overall, 26 patients with neck pain were randomly assigned to two groups: NM or control. In these participants, respiratory function and active cervical range of motion were assessed before and after intervention. Furthermore, the participants were provided a visual analog scale (VAS) and Fremantle Neck Awareness Questionnaire (FreNAQ). Each participant underwent 15 treatment sessions (5 days per week for 3 weeks). Further, in the NM group, in addition to conventional treatment, 10 sessions of neural mobilization were performed.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effect of Superficial EMG Biofeedback Training on Muscle Activation, Proprioception, Reaction Time and Upper Extremity Functions in Patients With Chronic Neck Pain: A Single-Blind Randomized Controlled Trial
NCT06896487
Mobilization With Movement Technique on the Stiffness of Cervical Muscles in Individuals With Mechanical Neck Pain
NCT06396104
Acute Effect of Neural Mobilization in Cervical Radiculopathy: A Randomized Controlled Study
NCT05887427
Comparison of the Different Exercises on Chronic Neck Pain
NCT05488756
Investigation of the Efficacy of Rocabado Exercises in Individuals With Chronic Neck Pain
NCT05887349
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Neural Mobilization Group
Each participant underwent 15 treatment sessions (5 days per week for 3 weeks). Further, in the NM group, in addition to conventional treatment, 10 sessions of neural mobilization were performed.
Neural Mobilization
Radial Nerve Mobilization, Medial Mobilization, Ulnar Mobilization
Control Group
Each participant underwent 15 treatment sessions (5 days per week for 3 weeks).
Neural Mobilization
Radial Nerve Mobilization, Medial Mobilization, Ulnar Mobilization
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Neural Mobilization
Radial Nerve Mobilization, Medial Mobilization, Ulnar Mobilization
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* those with neck pain for \>3 months
* those with complaints of pain, tension
* numbness on neurodynamic nerve tests
Exclusion Criteria
* neurological diagnosis, malignancy,
* upper extremity vascular problems,
* osteoporosis,
* pregnancy,
* history of newly repaired peripheral nerves,
* inflammatory processes,
* cervical spine and upper extremity surgeries,
* conditions affecting lung capacity (such as asthma, bronchitis, and diabetes mellitus)
25 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Okan University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Emine Atıcı
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Elif Tunç, Msc
Role: STUDY_DIRECTOR
Medical Park Gebze Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Medical Park Gebze Hosptal
Gebze, Kocaeli, Turkey (Türkiye)
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.
009
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.