![]() Significant differences (p < 0.05) were found in favor of the intervention group for all dimensions at the last assessment. Health-related quality of life was measured with Short Form-36 (SF-36), in 5 assessments: at baseline, after intervention period and at 1, 3 and 6 months after intervention.įor both groups, SF-36 mean values increased in all dimensions in every assessment. ![]() ![]() Both interventions lasted 2 weeks, 2 sessions per week. Subjects in the intervention group (n = 65) were treated with Deep Dry Needling in active myofascial trigger points plus stretching in neck muscles Control group (n = 65) received only stretching. One hundred thirty subjects with chronic non-specific neck pain and active myofascial trigger points in neck muscles were randomly allocated into two groups. The purpose of the study was to examine the effectiveness of Deep Dry Needling of myofascial trigger points on health-related quality of life improvement, as a secondary analysis, in people with chronic non-specific neck pain.Ī randomized parallel-group blinded controlled clinical trial was conducted at a public Primary Health Care Centre in Madrid, Spain, from January 2011 to September 2014. Currently, Deep Dry Needling is emerging as an alternative for improving symptoms and consequently, the quality of life in patients with chronic non-specific neck pain. There are some effective conservative Physical therapy interventions for treating chronic non-specific neck pain. The aforementioned factors are strongly related and may lead to a negative impact on health-related quality of life. The trial was registered on and at the Regional Scientific Ethics Committee of Southern Denmark S-20100069.Ĭhronic non-specific neck pain is related to limited cervical mobility, impaired function, neck muscles myofascial pain syndrome, and stress at work. This multimodal intervention may be an effective intervention for chronic neck pain patients. Per protocol analyses confirmed these results with additional significant improvements in the exercise group compared with controls. ![]() The exercise group showed statistically significant improvement in physical HR-QoL, mental HR-QoL, depression, cervical pressure pain threshold, cervical extension movement, muscle function, and oculomotion. Patient-reported outcome measures (Short Form-36 Physical and Mental component summary scores, EuroQol-5D, Beck Depression Inventory-II, Neck Disability Index, Pain Bothersomeness, Patient-Specific Functioning Scale, Tampa Scale of Kinesiophobia, Global Perceived Effect) and clinical tests (Aastrand Physical Fitness, cervical Range of Motion, Pressure Pain Threshold at infraspinatus, tibialis anterior and cervical spine, Cranio-cervical Flexion, Cervical Extension muscle function, and oculomotion) were recorded at baseline and after 4 months. The exercise group received additional exercises for neck/shoulder, balance and oculomotor function, plus graded physical activity training. To investigate the effect of combining pain education, specific exercises and graded physical activity training (exercise) compared with pain education alone (control) on physical health-related quality of life (HR-QoL) in chronic neck pain patients.Ī multicentre randomised controlled trial of 200 neck pain patients receiving pain education.
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