Comparison of Vibration Applied to the Trigger Point and Dry Needle in Acute Myofascial Pain Syndrome: a Prospective Randomized Controlled Research
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 2
- 主要终点
- Pressure pain threshold
研究概览
简要总结
The aim of this study is to compare the effects of localized vibration and dry needling applied to the trigger point in the individuals with acute myofascial pain syndrome.Pressure pain threshold (PPT) was used for the primary outcome measure of the study, and pain intensity, pain tolerance and short form (SF-36) were used for secondary outcome measures.
详细描述
The patients were divided into two groups as dry needling and localized vibration using the permuted block randomization method. The study was completed with 20 (17 women, 3 men) in the dry needling group and 20 in localized vibration (15 women, 5 men). In both applications, a total of 3 sessions were made to the patients at 1-day intervals.Patients' age, gender, duration of pain, localization, presence of additional disease, drug use were questioned and recorded. Pressure pain threshold (PPT) was used for the primary outcome measure of the study, and pain intensity, pain tolerance and short form (SF-36) were used for secondary outcome measures. All evaluation criteria except SF-36 were made before, immediately after and 1 day after each session, 1 week after the last session. SF-36 was evaluated before the 1st session treatment, after the 3rd session treatment and 1 week after the 3rd session treatment.
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
- Double (Participant, Outcomes Assessor)
盲法说明
Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •At least one active myofascial trigger point in the upper trapezius muscle
- •Symptoms lasting 1 day to 2 weeks
- •Cases who did not receive any physical therapy or medication to relieve pain
排除标准
- •Sensory defect in the area to be treated with vibration
- •Active inflammatory, rheumatological or infectious disease
- •Peripheral nerve lesions such as polyneuropathy, radiculopathy
- •Having a cardiac disorder (rhythm / conduction disorder, cardiac pacemaker, ischemic heart disease)
- •Diagnosis of fibromyalgia or other common musculoskeletal pain syndromes with an intact skin surface in the area to be vibrated
- •Patients with a history of panic attacks
结局指标
主要结局
Pressure pain threshold
时间窗: Change from baseline pressure pain threshold score at immediately after, 1 day after and 1 week after the last session
The test determines the amount of pressure over a given area in which a steadily increasing nonpainful pressure stimulus turns into a painful pressure sensation
次要结局
- Pain tolerance(Change from baseline Pain tolerance score at immediately after, 1 day after and 1 week after the last session)
- Visual analog scale(Change from baseline VAS score at immediately after, 1 day after and 1 week after the last session)
- Short Form 36 (SF-36)(Change from baseline Short Form 36 score at immediately after the 3rd session and 1 week after the treatment)