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Enrolling by invitation Not applicable

Manual Therapy Techniques for Cervical Pain: Algometric Evaluation

NCT06982456 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2025-05-19
Last updated
2025-05-21

Condition(s) studied

Myofascial Pain SyndromesMassageStretching

Investigational drug(s) / intervention(s)

Manual Therapy on the Upper Trapezius with or without Passive Stretching

Manual Therapy on the Upper Trapezius with or without Passive Stretching: The intervention consists of manual therapy techniques applied to the upper fibers of the trapezius muscle, including superficial massage, deep massage, and pressure release technique. In one of the experimental groups, this treatment is followed by passive stretching. The control group receives no intervention. Algometric measurements (pressure pain threshold) are taken before and after the intervention, and at one-week and two-week follow-up points to assess the effectiveness and persistence of the treatment.

Study summary

The main objective of this study is to evaluate the effectiveness of different manual therapy techniques in the treatment of cervical pain related to the upper trapezius muscle.

The intervention will compare the effects of superficial massage, deep massage, and pressure release technique on pain intensity, assessed through algometry.

Additionally, the study aims to determine whether the application of passive stretching following manual treatment leads to a significantly greater reduction in pain compared to groups that do not receive stretching.

Finally, the persistence of treatment effects will be evaluated one and two weeks after the intervention.

Eligibility

Sex
ALL
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * Be an undergraduate student in Physiotherapy. * Be between 18 and 40 years old. * Have experienced cervical pain at least once in their life. * Present pain localized in the upper fibers of the trapezius muscle. * Voluntarily agree to participate in the study by signing an informed consent form. Exclusion Criteria: * Suffer from migraines. * Have any diagnosed neurological disorders. * Have suffered a recent injury or trauma in the cervical region. * Have scoliosis or any other relevant spinal pathology. * Present any musculoskeletal condition that could interfere with the study outcomes.

Primary outcome measure(s)

  • PPT - Pressure Pain Threshold — Three weeks
    Pressure Pain Threshold (PPT) measured with an algometer (kg/cm²) on the upper trapezius fibers. Measurements will be taken pre-treatment, immediately post-treatment, and at one and two weeks post-intervention.

Trial sites (1)

FacilityCityRegionStatus
Universidad de Murcia Murcia Spain
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06982456 on ClinicalTrials.gov ↗ ← All trials in Spain