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N/A N=38 Randomized Double-blind Treatment

Efficacy of Capacitive-Resistive Therapy on the Treatment of Myofascial Pain

Myofascial Pain Syndrome of Neck

Enrolled (actual)
38
Serious AEs
0.0%
Results posted
Apr 2020
Primary outcome: Primary: Visual Analog Scale (VAS) Score Change — 5.9; 5.1; 4.1; 2.3 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Capacitive-Resistive Therapy (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Istanbul University
Primary completion
Mar 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Visual Analog Scale (VAS) Score Change
5.9; 5.1; 4.1; 2.3
PRIMARY
Pain Pressure Threshold (PPT) Score Change
2.0; 2.2; 2.8; 3.1; 2.5; 2.4
SECONDARY
Neck Disability Index (NDI) Score Change
28.0; 24.0; 19.7; 12.9
SECONDARY
Cervical Range of Motion (cROM) Change
60; 63; 65; 66; 59; 70
SECONDARY
Short Form - 36 (SF-36) Score Change
77; 71; 80; 79; 60; 61

Summary

Myofascial pain syndrome (MPS) is a painful musculoskeletal condition affecting the individuals' daily life presenting with muscle spasm, referred pain patterns, stiffness, restricted range of motion caused by trigger points. Capacitive-resistive diathermy therapy heats deep tissues by transferring energy through radiofrequency waves. Currently, although this modality is used to treat various acute or chronic musculoskeletal disorders, there is no specific data about myofascial trigger points in the literature. The investigators aimed to evaluate the efficacy of capacitive-resistive diathermy on the myofascial trigger point of neck/upper trapezius muscle area compared with the sham intervention of capacitive-resistive diathermy. Volunteers with active myofascial trigger points in the upper trapezius and neck were included the study after being examined by sports medicine specialists. Exclusion criteria were fibromyalgia, discal hernia, radiculopathy, myelopathy, having received trigger point injection and physical therapy within the last 1 month, neck or back surgery, rheumatismal diseases, pregnancy. Patients were randomly allocated into two groups. Group 1 will be treated with capacitive resistive diathermy and exercise. Group 2 will be treated with placebo (sham) capacitive-resistive diathermy and exercise for 10 sessions at intervals of 24-48 hours. Visual analog scale (VAS), neck disability index (NDI) score, cervical range of motion (cROM), active trigger point numbers will be evaluated before and after treatment. The study was designed as a prospective, randomized, placebo-controlled double-blind trial. The study was approved by the Istanbul Faculty of Medicine Ethics Committee. All participants were informed of the study and signed written informed consent.

Eligibility Criteria

Inclusion Criteria

  • Volunteers
  • Active myofascial trigger points in the upper trapezius and neck

Exclusion Criteria

  • Fibromyalgia
  • Discal Hernia
  • Radiculopathy, Myelopathy
  • Having received trigger point injection and physical therapy within the last 1 month
  • Neck or Back surgery
  • Rheumatismal diseases
  • Pregnancy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04287517). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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