Neck Pain
Conditions
Keywords
Neck Pain, Needling, Expectance
Brief summary
Dry needling (DN) is a treatment technique used for treating musculoskeletal pain conditions. DN has shown to be effective on pain and function in patients with mechanical neck pain. Potential effects of DN can be related to several mechanisms, including physical, cognitive and emotional factors. This study will evaluate the role of the patient expectances related to the evolution (progress) of the condition, in this case, mechanical neck pain, in the effects of real or sham dry needling in sensitivity outcomes such as pain intensity or pressure pain sensitivity. Expectation of each patient in both groups will be considered positive, neutral or negative based on the outcomes of the Patient Shoulder Expectancies (PSOE) questionnaire which was adapted to the cervical spine.
Interventions
DEVICEDry Needling
Real dry needling will be conducted according to the fast-in and fast-out principle. The intervention will be applied until a total of four local twitch responses will be elicited
DEVICESham Needling
Sham dry needling with be conducted with a sham needle device. This needle has a blunt tip and retractable handle that created the illusion of a needle penetrating the skin. When this needle touches the skin, a pricking sensation will be created. However, when pressure will be increased, the shaft of the needle disappears into the handle creating a sensation on the patient
Sponsors
Universidad Rey Juan Carlos
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Months to 65 Months
Healthy volunteers
No
Inclusion criteria
* Non-specific mechanical neck pain of at least 3 months of duration * At least one active trigger point in the upper trapezius muscle which referred pain reproduces the neck pain symptoms
Exclusion criteria
* whiplash injury; * previous cervical or thoracic surgery; * cervical radiculopathy or myelopathy; * diagnosis of fibromyalgia syndrome; * having undergone physical therapy in the previous 6 months; * fear to needles
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in Neck Pain Intensity between baseline and follow-up periods | Baseline, immediately after and 1 week after intervention | The intensity of neck pain at rest and during active movement of the cervical spine in rotation will be assessed with a visual analogue scale (VAS). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in Pressure pain sensitivity between baseline and follow-up periods | Baseline, immediately after and 1 week after intervention | Pressure pain thresholds (PPT) will be assessed at the upper trapezius muscle, spinous process of C7 and distant pain-free area of the lower extremity (heel) |
| Changes in patients self-perceived improvement between baseline and follow-up periods | Baseline and 1 week after intervention | Patients self-perceived improvement will be assessed using a Global Rating of Change (GROC) consisting of a 15-point scale ranging from -7 (a very great deal worse) to +7 (a very great deal better). |
Countries
Spain
Outcome results
None listed