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Recruiting NCT07120659

Vacuum Massage vs Tactile Massage for the Treatment of Chronic Neck Pain

Trial Parameters

Condition Chronic Neck Pain
Sponsor University of Tromso
Study Type INTERVENTIONAL
Phase N/A
Enrollment 60
Sex ALL
Min Age 21 Years
Max Age 75 Years
Start Date 2025-10-27
Completion 2027-12-31
Interventions
soft touch massagevacuum massage

Brief Summary

Chronic pain significantly impacts individuals and society, with about 30% of Norwegian adults affected, making it the leading cause of long-term sick leave and disability benefits. Concerns over addiction to pain medications highlight the need for non-pharmacological treatments, though many such therapies, often complementary or alternative, are not widely available in conventional healthcare. Unclear biomechanisms of these therapies pose challenges for clinical trials and acceptance. This pilot study aims to explore the effects of two types of massage-cupping massage (CM, intense) and tactile massage (TM, soft)-on chronic neck pain, focusing on their mechanisms of action. Quantitative sensory testing (QST) will be used as a biomarker to assess changes in the pain pathway. A previous feasibility study on CM and QST conducted in Germany informs this research. The study will recruit 60 patients with chronic neck pain, randomized to CM or TM, with six weekly treatment sessions. QST will be measured before and after treatment to understand therapy-induced changes in the pain pathway. Findings will help tailor massage therapies to individual needs, improve clinical trial quality, and promote the integration of non-pharmacological treatments into conventional care, benefiting a large population in need.

Eligibility Criteria

Inclusion Criteria: * suffer from non-specific neck pain persisting at least 3 months * mean pain intensity ≥ 50 on a 0-100 mm visual analogue scale (NRS) with "0" meaning "no pain" and "100" meaning "worst pain imaginable" Exclusion Criteria: * neurological symptoms * having had a vertebral column surgery less than 12 months prior to the study, * have received TENS, acupuncture, osteopathy, or a chiropractic maneuver or infiltration at the area within 4 weeks prior to the inclusion in the study * suffer from a congenital deformation of the spine.

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