Examination of the Efficacy of ESWT (Extracorporeal Shock Wave Therapy) and TENS (Transcutaneous Electrical Nerve Stimulation) in Individuals Receiving Drug Treatment for Chronic Pelvic Pain Syndrome: Randomized Controlled Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 38
- 试验地点
- 2
- 主要终点
- National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI)
研究概览
简要总结
The aim of this study is to evaluate the effectiveness of ESWT (Extracorporeal Shock Wave Therapy) and TENS (Transcutaneous Electrical Nerve Stimulation) in individuals diagnosed with chronic pelvic pain syndrome and treated with medication. The study was organized as a randomized controlled trial. The sample size is 30 patients suffering from chronic pelvic pain syndrome.
详细描述
Volunteers who are between the ages of 20-40, diagnosed with chronic pelvic pain syndrome, and who meet the inclusion criteria will be included in the study and will be randomized into 2 groups: Group I (TENS) and Group II (ESWT).
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 40 Years（Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Aged between 20-40 years old males
- •Diagnosis of Chronic Pelvic Pain Syndrome
排除标准
- •Surgery related to pelvic floor
- •2. Receiving drug treatment
结局指标
主要结局
National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI)
时间窗: baseline and immediately after the intervention
This assesses the quality of life. The index has sub dimensions(pain, urinary symptoms, quality of life impact). The score evaluation of the pain scale is between 1 and 21 points, the score evaluation of the urination scale is between 0 and 10 points, and the score evaluation of the quality of life scale is between 0 and 12 points.
VISUAL ANALOUGE SCALE
时间窗: baseline and immediately after the intervention
It evaluates pain intensity grading between 0-10. Higher score shows severe pain.
ALGOMETER
时间窗: baseline and immediately after the intervention
This evaluates pain tolerance threshold of the patients.The less score shows pain intolerance.
次要结局
- Hospital Anxiety and Depression Scale- HAD(baseline and immediately after the intervention)
- Lasegue Test(baseline and immediately after the intervention)
- Nottingham Health Profile-NHP(baseline and immediately after the intervention)
- Digital Muscle Testing(baseline and immediately after the intervention)
- Flexibility Measurements(baseline and immediately after the intervention)
- ROM Assessments(baseline and immediately after the intervention)
研究者
Ugur Cavlak
Clinical Professor
Biruni University