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Chronic Mechanical Neck Pain clinical trials

View clinical trials related to Chronic Mechanical Neck Pain.

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NCT ID: NCT05845853 Recruiting - Clinical trials for Chronic Mechanical Neck Pain

Scapular Motor Control for Chronic Mechanical Neck Pain

Start date: May 1, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of motor control training using scapular PNF exercise on neck pain, function, proprioception, and scapular muscle strength in patients with chronic mechanical neck pain.

NCT ID: NCT05600647 Completed - Clinical trials for Chronic Mechanical Neck Pain

Magnetic Therapy Versus Exercise Therapy in Old Patients With Chronic Mechanical Neck Pain

Start date: October 21, 2020
Phase: N/A
Study type: Interventional

Mechanical neck pain (MNP) is a common condition that affects all aging groups. MNP has a huge physical, psychological and economic impact. The aim of this study is to evaluate the effects of magnetic therapy (MT) with exercise versus exercise therapy on neck pain, proprioception, balance, and function in older patients with chronic MNP. Materials & Method: 50 male and female patients with chronic MNP, their ages will range from 56 years and above. They will be allocated from different physiotherapy departments. Eligible participants will be equally randomized into two groups. Group-I: 25 patients will practice the exercise training program in addition to receiving pulsed electromagnetic field therapy (PEMF) (experimental arm). Group-II: 25 patients will practice the exercise program. All participants will receive three sessions every week for four weeks. The primary outcomes are pain (Visual Analogue Scale VAS) and balance (Single leg stance time test SLST, Tinetti balance assessment, and Timed Up and Go TUG). The secondary outcomes are the Neck Disability Index (NDI), cervical range of motion (CROM), cervical joint position sense error (JPSE), and quality of life QOL SF-36 questionnaire. Measurements will be taken before the first session, after two weeks, and after the last session.

NCT ID: NCT05557747 Completed - Clinical trials for Chronic Mechanical Neck Pain

Cervicothoracic Junction Mobilization Versus Muscle Energy Technique in Chronic Neck Pain

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

This study will be conducted to identify the difference between the effect of of cervicothoracic junction mobilization and autogenic Muscle Energy Technique. on neck pain, cervical range of motion, cervical proprioception and neck disability in mechanical neck pain patients with cervicothoracic junction hypomobility.

NCT ID: NCT04777890 Completed - Clinical trials for Chronic Mechanical Neck Pain

Effects of Instrumental and Manipulative Techniques for the Suboccipital Region in Subjects With Chronic Mechanical Neck Pain

Start date: March 20, 2021
Phase: N/A
Study type: Interventional

The aim of the study is to compare the effectiveness between the suboccipital inhibition technique, the suboccipital inhibition carried out with the INYBI instrument and the suboccipital inhibition with the INYBI plus the upper cervical manipulation, all in patients with chronic mechanic cervicalgia, and to determine which of these techniques is the most effective in the variables studied. In order to do so, 96 subjects participated in the study, being assigned to the 3 intervention groups. We expected the combined treatment (INYBI instrument + upper cervical manipulation) to be the one to produce the best results.

NCT ID: NCT01772966 Completed - Clinical trials for Chronic Mechanical Neck Pain

Chiropractic Manual Therapy and Neck Pain

Start date: February 2013
Phase: N/A
Study type: Interventional

Eligible subjects with chronic neck pain will be randomly allocated to one of two intervention groups: real vs control spinal manipulation. They will receive three intervention sessions. H1: Chronic neck pain patients treated longitudinally over a series of three encounters in one week by random assignment to treatment group with either of the dual delivery procedures (Intervention 1=typical-control or Intervention 2=control-control) will have a 50% error rate of self-report of group allocation at exit interview. H2: Patients treated by the typical-control dual procedure over a typical sequence of encounters (3 times in one week) will show statistically significant improvement in clinical outcomes; defined quantitatively by visual analogue pain scale (VAS), Neck Disability Index (NDI), range of motion and pressure algometry; compared to those treated by the control-control dual procedure. H3: Patients stratified by 'a priori' patient expectation for treatment outcome will show no significant difference in self-report of group allocation or clinical outcome measures. A total of 372 subjects will be recruited.