Tokyo, Oct. 3 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000063157) titled 'Comparison of the Effect of Neck Stabilization Exercises with and without Pain Neuroscience Education on Pain, Functional Disability, Range of motion and Proprioception in clients with NonSpecific Chronic Neck Pain.' on Oct. 3.

Study Type: Interventional

Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Single blind -investigator(s) and assessor(s) are blinded Control - No treatment

Primary Sponsor: Institute - self funding

Condition: Condition - pre test - post test Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - The primary objective of this study is to compare the effect of neck stabilization exercises with and without pain neuroscience education (PNE) on pain, functional disability, range of motion, and proprioception in patients with chronic nonspecific neck pain. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - Neck stabilization exercises Interventions/Control_2 - Combined (stabilization + PNE)

Eligibility: Age-lower limit - 25 years-old = Gender - Male and Female Key inclusion criteria - Men and women aged years with normal body mass index (BMI). No fracture, dislocation, or disc herniation in the cervical spine. No other chronic pain in other body regions. No history of invasive or minimally invasive spinal treatments. No use of psychotropic or neurological medications. No migraine (screened using a questionnaire). No obvious postural deformities or other visually detectable abnormalities that could affect the study. Chronic nonspecific neck pain lasting more than 3 months. Pain intensity between 5 and 7 on the Visual Analogue Scale (VAS). Willingness to participate in the corrective exercise program. Willingness to participate in the study and sign informed consent. Key exclusion criteria - Irregular attendance at training sessions: missing 2 consecutive sessions or 3 total sessions. Failure to complete the pre-test and post-test assessments. Pain exacerbation during the exercise protocol. Development of musculoskeletal pain in other body regions during the study. Target Size - 51

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2026 Year 09 Month 13 Day Date of IRB - 2026 Year 08 Month 01 Day Anticipated trial start date - 2026 Year 10 Month 03 Day Last follow-up date - 2026 Year 11 Month 16 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000072275

Disclaimer: Curated by HT Syndication.