Effects of Dry Needling With a Standard Exercise Programme on Pain and Quality of Life in Patients With Chronic Mechanical Neck Pain

Neck Pain Clinical Trial

Official title: Effects of Dry Needling With a Standard Exercise Programme on Pain and Quality of Life in Patients With Chronic Mechanical Neck Pain

Status Completed

Clinical Trial Summary

Abstract\sBackground Physical therapists frequently utilize dry needling (DN), which focuses on trigger points and non-trigger point structures, to treat mechanical neck pain (MNP). It is an invasive procedure that involves inserting solid fiber needles into myofascial trigger points or hyperirritable nodules that are painful to the touch. This procedure can affect the motor and autonomic neurons and relieve pain. Objectives examining the short-term effects of dry needling in combination with a standardized exercise program on pain and quality of life in chronic mechanical neck pain Methods The allocation of 18 participants to the DN or Exercise intervention groups will be done at random. Before the exam, the Beck Depression Inventory (BDI), Neck Disability Index (NDI), Short Form-36 Quality of Life Scale, and Numerical Rating Scale (NPS-11) will be evaluated. Analytical Statistics For the statistical analysis of the data, SPSS 23.0 will be employed. The "Kolmogorov-Smirnov test" will be used to determine whether the data are distributed normally. The effectiveness of each intervention will be determined using a paired t test, and between-group comparisons will be made using an independent t test. The distribution of categorical variables will be compared using a chi-square test. A 95% confidence interval and p0.05 will be used to determine significance. Key words: mechanical neck pain, dry needling, neck exercises, and quality of life.

Clinical Trial Description

Procedure The lead investigator screened the participants to ensure that they met the requirements for participation in the study. The participants were randomly divided into the "control group" and the "experimental group." Intervention Needling dry The experimental group will receive dry needling in addition to the exercise routine, while the control group will just receive the exercise protocol. The trigger point (TrP) DN will be used, and a TrP location will be palpated and designated for needle insertion in the upper trapezius muscle. Stainless-steel disposable needles 0.3 30 mm; Novasan, S.A. The needle will be placed into the skin for up to 10 to 15 mm, until a local twitch reaction is felt, and the person will be monitored for two weeks after that. For two weeks, the participant will begin the workouts once daily. Protocol for neck exercise: Both the experimental and control groups will get a standardized workout regimen that included neck and upper back muscular stretching and strengthening. Confidentiality: Data will be collected collectively and maintained confidentially in a computer protected by a password; no individual's name will be revealed. ;

Related Conditions & MeSH terms

• Neck Pain

• NCT number: NCT05220852
• Study type: Interventional
• Source: Imam Abdulrahman Bin Faisal University
• Status: Completed
• Phase: Phase 3
• Start date: February 6, 2022
• Completion date: August 9, 2022