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Neck Pain Musculoskeletal clinical trials

View clinical trials related to Neck Pain Musculoskeletal.

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NCT ID: NCT06167525 Not yet recruiting - Clinical trials for Neck Pain Musculoskeletal

Neck Posturing in Surgeons During Microsurgery Procedures Using Upright Go 2 Device

Start date: January 18, 2024
Phase: N/A
Study type: Interventional

Consultant and senior registrars performing microsurgery will be invited to participate in this Study. The study will take place at single site (Beaumont Hospital). A questionnaire to collect demographic information (age, height, sex, year of training, prior neck trauma or know neck issues) will be given to the consented surgeons. Additionally, surgery characteristics will be recorded (procedure, surgeon role (i.e lead or assisting), table height, frequency of adjustment of table height, and use of sitting or step stool, headlight, and/or loupes for >50% of the procedure). A postural training device, Upright Go 2 will be positioned at the spinous process of the cervical vertebrae of each surgeon and used to measure neck positions during microsurgical procedures. The device will be calibrated to an ideal neutral cervical spine position, so that excessive flexion and extension of the neck can be recorded. The device contains built-in sensors that provide bio-feedback in the form of gentle vibrations if posture has deviated from neutral position. During the first stage of the study the device will be set to record cervical spine positioning without bio-feedback signals. This will be used to record duration of time surgeons held maladaptation postures. The second stage will involve real-time feedback through the device. For surgeons who consent, bio-feedback signals will be given once deviated from a neutral posture for >1 minute. Response of surgeons to bio-feedback signals will also be recorded. The Neck Disability index score will be used to assess for neck pain and the functional implications in relation to reported neck pain. This will be completed following study completion.

NCT ID: NCT02806323 Completed - Clinical trials for Neck Pain Musculoskeletal

Individually Tailored Yoga Program for the Treatment of Chronic Neck and Back Pain

Start date: July 1, 2016
Phase: N/A
Study type: Interventional

The goal of this pilot study is to determine the feasibility of an individually tailored yoga program delivered in a group setting for the treatment of chronic neck and back pain in a low income population. Chronic pain is one of the most common, costly, and disabling conditions, and is often refractory to treatment. Yoga is a promising treatment for chronic pain. This pilot study will test the hypothesis that study subjects will participate in a voluntary 12 week yoga intervention for the treatment of chronic neck and back pain, as assessed by attendance at 12 weekly yoga practice sessions. Secondary outcomes will include change in pain and quality of life scores over the 12 week study period as assessed by the Visual Analog Scale for Pain Severity and EQ-5D-3L.

NCT ID: NCT02424032 Recruiting - Clinical trials for Neck Pain Musculoskeletal

Stabilization Exercises With and Without Connective Tissue Massage for Chronic Mechanical Neck Pain

Start date: February 2013
Phase: Phase 2
Study type: Interventional

The aim of this study was to investigate and compared the effects of cervical and scapulothoracic stabilization exercises with and without connective tissue massage (CTM) for patients with chronic mechanical neck pain.

NCT ID: NCT01289964 Completed - Neck Pain Clinical Trials

The Effect of 5 Times Dry Cupping in the Treatment of Chronic Neck Pain

TS
Start date: July 2009
Phase: N/A
Study type: Interventional

The study aims to investigate the influence of 5 dry cupping treatments on chronic non specific neck pain. 50 patients with neck pain are randomised into cupping treatment and waiting list control group at T0 (Day 0). At T1 (Day 7)the investigators evaluate the neck pain (VAS), the neck related disability (NDI), pain related to movement (PRTM) and the quality of life (SF36). To investigate neurophysiological effects of cupping we also measure mechanical detection threshold (MDT), vibration detection threshold (VDT) and pressure pain threshold (PPT) at pain related and control areas. The treatment group then receives 5 cupping treatments over a period of two weeks. After the cupping series resp. a waiting period for the waiting list control group (T2, Day 25) all measurements from T1 are repeated (VAS, NDI, PRTM, SF36, MDT, PPT, VDT). At last, a pain and medication diary is filled in by the patients from T0(Day 0) until T2 (Day 25). The investigators hypothesize, that cupping treatment is effective against neck pain (diary, VAS, NDI, PRTM, SF36) and that it leads to changes on perceptual level (MDT, VDT, PPT), when compared to the waiting list control group.

NCT ID: NCT00741650 Completed - Clinical trials for Neck Pain Musculoskeletal

Ibedrift- A Trial Comparing a New Approach to Musculoskeletal Pain Consisting of Education and Peer Involvement to Treatment as Usual

Ibedrift
Start date: September 2008
Phase: Phase 2/Phase 3
Study type: Interventional

A randomized controlled trial comparing a new approach to musculoskeletal pain consisting of education and peer involvement to treatment as usual. All local government employees in 1-3 Norwegian municipalities will be invited to participate.