Chronic Neck Pain Clinical Trial
Official title:
The Effectiveness of Manual Therapy to the Cervical Spine and Diaphragm,Combined With Breathing Reeducation Exercises, in Patients With Non-specific Chronic Neck Pain: A Randomized Controlled Trial
Verified date | November 2023 |
Source | University of West Attica |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Chronic neck pain (CNP) is reported to be one of the most common musculoskeletal pain syndromes. Studies showed that patients with chronic neck pain compensated with changes in Pain, Function, Musculoskeletal and Respiratory outcomes. The diaphragm is a primary respiratory muscle contributing to postural stability and spinal control. Many studies showed that manual therapy and exercise improve clinical and respiratory outcomes in CNP patients. Few studies highlight the importance of diaphragm manual therapy and Reeducation Breathing Exercises in musculoskeletal diseases and in CNP patients. However, the exact mechanism is still unclear. This study aims to examine the hypothesis that: "Diaphragm Manual Therapy and Breathing Reeducation Exercises combined with cervical manual therapy - improve clinical and respiratory outcomes more than cervical manual therapy intervention only or conventional physiotherapy
Status | Completed |
Enrollment | 90 |
Est. completion date | November 21, 2023 |
Est. primary completion date | November 21, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 25 Years to 65 Years |
Eligibility | Inclusion Criteria: - Individuals who have pain for at least 3 months with non-specific mechanical neck pain - Individuals voluntarily participating in the study - Patients will also be selected on the basis of demonstrating DB in at least one of a series of tests conducted to assess the extent of their Dysfunctional Breathing (biomechanical, biochemical, psychological) Exclusion Criteria: - Pregnancy - Contraindications for manual therapy or inability to complete the treatment - Patients who received physiotherapy or osteopathic treatment during the last 3 months - Individuals with bronchial asthma, chronic bronchitis, emphysema, bronchiectasis and malignancy - Medical diagnosis of rheumatologic disease - Medical diagnosis of respiratory disease (COPD, asthma) - Spine surgery (cervical, spinal, thoracic or abdominal region) - Medical diagnosis of cancer (past or present) - Whiplash injuries - Previous cervical fracture - Cervical anatomical changes - Thrombotic events, Anaemia or Diabetes - Body temperature greater than 37 degrees in the previous 48 hours - Obesity (BMI greater than 40) - Scoliosis or other diseases that cause spine and chest deformity - Positive cervical region instability and positive vertebral artery test - Individuals with neurological deficits or with motor loss - Individuals who have whiplash injuries, osteoporosis, or rheumatoid disease (such as rheumatoid arthritis, systemic lupus erythematosus, Sjögren's syndrome) |
Country | Name | City | State |
---|---|---|---|
Greece | Tatsios Petros | Glyfada | Athens |
Lead Sponsor | Collaborator |
---|---|
University of West Attica |
Greece,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Neck Disability Index (NDI) | The NDI consists of 10 sections. Each section is scored on a 0 (no pain) to 5 (worst imaginable pain) rating scale. Points summed to a total score. The test can be interpreted as a raw score, with a maximum score of 50, or as a percentage. | change from baseline up to 4 weeks and up to 3 months | |
Primary | Pain Intensity VAS | Visual Analog Scale: Minimum value = 0 (Best outcome); Maximum value = 100 (Worst Outcome) | change from baseline up to 4 weeks and up to 3 months | |
Secondary | Change in Range of motion (ROM) | A smartphone-based application and KFORCE SENS electronic goniometer, KINVENT, France will be used to accurately measure ROM during neck movements of Flexion-Extension, Left-Right Side Flexion, and Left-Right Rotation. | change from baseline up to 4 weeks and up to 3 months | |
Secondary | Craniovertebral Angle | Lateral Photography- examination of the FHP through lateral photographs can provide very reliable estimates. The reliability remained high in both the sitting and standing position. | change from baseline up to 4 weeks and up to 3 months | |
Secondary | Nijmegen Questionnaire (NQ) | Screening tool used to detect patients with hyperventilation complaints and DB patterns. Scores>20 are used as the cut-score to identify DB in patients with various conditions. NQ values in healthy individuals range from 10 to 12 ± 7 and values do tend to decrease towards these levels after breathing retraining. | change from baseline up to 4 weeks and up to 3 months | |
Secondary | Hi-Lo test | A test that assesses breathing dysfunction. Instructions will be given to the examiners for how to perform and record the Hi-Lo: ''Examiner at the front and slightly to the side of the person have to place one hand on the sternum of the patient and the other hand on their upper abdomen. The examiner has to determine whether thoracic or abdominal motion is dominant during breathing and to what extent this is so. Also, has to check for paradoxical breathing. The extent of thoracic or abdominal breathing rate using a score between 1 and 3. | change from baseline up to 4 weeks and up to 3 months | |
Secondary | Single Breath Count (SBC) | A test that assesses breathing dysfunction. To perform, ask the patient to count out loud after maximal inspiration. The ability to reach 50 indicates normal respiratory function. | change from baseline up to 4 weeks and up to 3 months | |
Secondary | End Tidal CO2 (ETCO2) and Respiratory Rate (RR) | Measured by Capnography. ETCO2 less than 35 mmHg, RR of 16 breaths/min or more, will be considered as signs of respiratory pattern abnormality. | change from baseline up to 4 weeks and up to 3 months | |
Secondary | Breath Holding Time | A test that assesses DB. This test is an indicator of a person's respiratory response to biochemical, biomechanical, and psychological fac-tors, and it seems that abnormally, shortened, BHT may indicate abnormalities in the respiratory function that are closely related to DB. Participants will be instructed to assume a comfortable sitting position and breath usually and gently in and out and at the end of a normal exhalation, they will be asked to pinch their nose and hold their breath. The instruction is to hold their breath until they cannot hold their breath any longer and require breathing in again. According to Kiesel (2020) [30], a BHT <25 secs is con-sidered as a sign of DB. | change from baseline up to 4 weeks and up to 3 months | |
Secondary | Chest Expansion | The difference between the values obtained during deep inspiration and expiration will be determined by tape ruler (cm), high degrees represent better outcome, low degrees represent worse outcome | change from baseline up to 4 weeks and up to 3 months | |
Secondary | Hospital and Anxiety Depression Scale (HADS) (Greek version 2007) | Assesses the level of anxiety and depression experienced by patients in a hospital outpatient clinic. A subscale score >8 denotes anxiety or depression. | change from baseline up to 4 weeks and up to 3 months | |
Secondary | Tampa Scale for Kinesiophobia (TSK) (Greek version 2005) | Kinesiophobia is one of the most frequently employed measures for assessing pain-related fear in pain patients through a 17-item questionnaire. | change from baseline up to 4 weeks and up to 3 months | |
Secondary | Adverse events | Through an interview, potential adverse effects are evaluated during and after the physiotherapy treatment. | change from baseline up to 4 weeks and up to 3 months |
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