Impacts of Static Magnetic Fields on Dysmenorrhea Pain
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Pain score scale of 1-10 / 1 being less pain 10 being more pain
研究概览
简要总结
Study to determine the effectiveness of a certain type of magnet to reduce period pain
详细描述
Young women with their period pain levels of 6 or greater on a pain scale of 0-10 will wear a concentric magnet or a sham that is positioned close to the maximum pain site. The pain score after wearing either the magnet or sham will be recorded.
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, Investigator)
盲法说明
Magnet and sham devices used weigh and look the same
入排标准
- 年龄范围
- 18 Years 至 35 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Female with period pain score consistently equal to or greater than 6 on a pain scale of 0-10 -
排除标准
- •Pain not experienced on almost all menstrual cycles
- •Having secondary dysmenorrhea including endometriosis, fibroids or pelvic inflammatory disease
- •Having a pacemaker or any implanted wires or devices -
研究组 & 干预措施
Magnet group
Women wearing magnet
a magnet, or sham device indistinguishable from the magnet (determined randomly), will be placed on her abdomen. If the pain is predominately in her abdomen, the device will be placed on the location with the most pain. If the pain is predominantly in the subjects back, the device will be placed on the lower abdomen on the midline between the umbilicus and the pubic bone.
干预措施: Magnet (Device)
Sham group
Women wearing sham
a magnet, or sham device indistinguishable from the magnet (determined randomly), will be placed on her abdomen. If the pain is predominately in her abdomen, the device will be placed on the location with the most pain. If the pain is predominantly in the subjects back, the device will be placed on the lower abdomen on the midline between the umbilicus and the pubic bone.
干预措施: Magnet (Device)
结局指标
主要结局
Pain score scale of 1-10 / 1 being less pain 10 being more pain
时间窗: 40 minutes
Subject reported pain after wearing device
次要结局
未报告次要终点