Treatment of Cervical Syndrome With Myofascial Therapies
- 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
- Patients of both sexes, aged between 20 and 60 years, in an active state of pain and diagnosed with muscle breakdown
- 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
Group Intervention Description EXPERIMENTAL GROUP Physiotherapy treatment Patients 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 GROUP Physiotherapy treatment Multimodal physical therapy program includes: * ultrasound therapy (US), * transcutaneous electric nerve stimulation (TENS) * massage.
- Primary Outcome Measures
Name Time Method The intensity of cervical pain Baseline 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
Name Time Method The intensity of cervical pain Eight 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 motion Baseline, four weeks and eight weeks Measured by goniometer type crom
Pressure pain thresholds in cervical trigger points Baseline, 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