The Effectiveness of Deep Tissue Massage on Pain, Trigger Point, Disability, Range of Motion and Quality of Life in Individuals With Myofascial Pain Syndrome
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 80
- 试验地点
- 2
- 主要终点
- Change from baseline in quality of life on the 36-point Short-Form 36(SF-36) at 4 week
研究概览
简要总结
This study aims to examine the effect of deep tissue massage (DTM) on myofascial trigger point (MTrP) number, neck range of motion (ROM), pain, disability and quality of life in patients with Myofacial pain syndrome (MPS).
详细描述
A total of 88 patients with MPS were screened for eligibility. Of these patients, 80 who met the inclusion criteria were randomly divided into two groups using randomization with computer-generated random numbers as the control group (n=40) and DTM group (n=40).
The patients were evaluated at baseline (Day 0), and the end of treatment (Week 4).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 20 Years 至 60 Years(Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Being over the age of 18
- •Have at least one active trigger point
- •Have not previously undergone local injectable anesthetic blockage or acupuncture,
- •Complaining of pain for the last three months
- •Getting a diagnosis of MPS
排除标准
- •Patients with infectious skin disease,
- •Using analgesic and antidepressant medication,
- •A history of major trauma or surgical intervention,
- •Mini Mental State Examination (MMSE) score ≤ 24 according
结局指标
主要结局
Change from baseline in quality of life on the 36-point Short-Form 36(SF-36) at 4 week
时间窗: Baseline and 4 week
Short form-36 (SF-36) was used to determine the quality of life. SF-36, which has a generic scale feature and provides wide angle measurement among the quality of life scales; Ware et al. It was developed and put into use in 1993. The scale includes items including perception of change in health in the last four weeks and perception of change in health in the last week. SF-36 Turkish validity and reliability study has been done. While the increase in the score negatively affects the body pain, physical and emotional role, it positively affects the parameters of physical function, vitality/energy, general health, mental health and social functioning.
Change from baseline in disability on the 20-point at 4 week Neck Pain and Disability Scale (NPDS) at 4 week
时间窗: Baseline and 4 week
The Neck Pain and Disability Scale (NPDS) was used for the assessment of disability. This scale was developed by Wheeler et al. NPDS is a 20-item questionnaire developed using VAS as a template. The questions investigate the intensity of pain and its interaction with professional, recreational and functional aspects of life, and the presence and extent of emotional factors related to these. The scoring of each question varies between 0-5. The range of points people can get varies between 0-100. High score values indicate severe disability in patients. NPDS is an index has Turkish reliability and validity, consisting of 20 questions and each question scored between 0 and 5. Increased NPDS scores indicate increased disability.
Change from baseline in number of trigger points on the manual palpation at 4 week
时间窗: Baseline and 4 week
Manual palpation of the trapezius and levator scapula muscles was performed by a trained physiotherapist in this field to assess the presence of MTrP. Palpation always bilateral was performed with the third and second fingers of each hand with a pressure of no more than 4 kg, which is the conventional approach for detecting tender and trigger points. We considered the pressure of more than 4 kg as whitening of the nail.
Change from baseline in neck pain on the 10-point Visual Analog Scale(VAS) at 4 week
时间窗: Baseline and 4 week
The severity of neck pain was assessed using the visual analog scale (VAS) consists of scores from 0 to 10 in a horizontal line of 10 cm. Patients are asked to mark a place on the scale according to the pain they feel. Increased VAS scores indicate increased pain.
Change from baseline in range of motion on the universal goniometer at 4 week
时间窗: Baseline and 4 week
A universal goniometer was used to evaluate the active neck range of motion (ROM) of the patients. The universal goniometer consists of a pivot point and two arms, fixed and movable. The fixed arm is kept fixed to the immobile part of the extremity or to the floor or body where the measurement is made. The movable arm is the arm that follows and makes the measurement throughout the movement of the measured joint. During our measurement, we chose the pivot point to be the acromion, the earlobe alignment for the movable arm and the fixed arm to be parallel to the ground.
次要结局
未报告次要终点
研究者
Ömer Bingölbali
lecturer
Muş Alparslan University
