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Treatment of Cervical Syndrome With Myofascial Therapies

Not Applicable
Completed
Conditions
Cervical Syndrome
Interventions
Procedure: Physiotherapy treatment
Registration Number
NCT03184220
Lead Sponsor
University of Cadiz
Brief Summary

This study aimed to investigate the effects of myofascial release therapy (MRT) for improving pressure pain thresholds (PPTs), range of motion and pain in patients with mechanical neck pain (NP).

Detailed Description

Fifty-four participants with NP were randomly allocated to either an MRT (five sessions) or a physical therapy (PT) groups (ten sessions) during two weeks. Multimodal PT program included: ultrasound therapy (US), transcutaneous electric nerve stimulation (TENS) and massage. Visual Analogue Scale (VAS), range of motion and (CROM) PPTs in sub-occipital and upper trapezius muscles were measured at baseline, at the end of treatment and at 1 month follow-up. T-tests and a repeated-measures multivariate analysis of variance (RM-MANOVA) were used for VAS, CROM and PPTs, respectively.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
54
Inclusion Criteria
  • Patients of both sexes, aged between 20 and 60 years, in an active state of pain and diagnosed with muscle breakdown
Exclusion Criteria
  • Patients who are pregnant, have pacemakers and surgically operated in the area to be treated

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
EXPERIMENTAL GROUPPhysiotherapy treatmentPatients who are pregnant, have pacemaker and those surgically operated cervical spine patients who have been treated with myofascial therapy a month earlier. Multimodal physical therapy program includes: Myofascial syndrome cervical therapy treatment.
CONTROL GROUPPhysiotherapy treatmentMultimodal physical therapy program includes: * ultrasound therapy (US), * transcutaneous electric nerve stimulation (TENS) * massage.
Primary Outcome Measures
NameTimeMethod
The intensity of cervical painBaseline

A 10-point Numerical Pain Rating Scale (NPRS; 0: no pain, 10: maximum pain) will be used to assess the patients' current level of cervical pain, and the worst and lowest level of pain experienced in the preceding week in the cervical area.

Secondary Outcome Measures
NameTimeMethod
The intensity of cervical painEight weeks

A 10-point Numerical Pain Rating Scale (NPRS; 0: no pain, 10: maximum pain) will be used to assess the patients' current level of cervical pain, and the worst and lowest level of pain experienced in the preceding week in the cervical area.

Active cervical range of motionBaseline, four weeks and eight weeks

Measured by goniometer type crom

Pressure pain thresholds in cervical trigger pointsBaseline, four weeks and eight weeks

Pressure pain thresholds (PPTs) will be measured with a pressure algometer (Baseline, Pain TestTM, Wagner Instruments). The clinimetric properties of this instrument have been evaluated previously. The PPT will the point at which pressure elicited pain and will presented as kilograms per square centimeter. All measurements will be conducted by the same well-trained physician.

Trial Locations

Locations (1)

Policlínica Santa maría

🇪🇸

Cadiz, Cádiz, Spain

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