CTRI/2022/01/039779招募中未知
Effective Quantification and Comparison among Dry Cupping, Scapulothoracic Mobilization, Foam Rolling in patients with Non-specific neck pain.
o sponsor0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Patient who will agree to fill the consent form
- •2. Patients with NDI score 10-45%.
- •3. Self report of unilateral or bilateral Non
- •specific neck Pain continuously within the 6 weeks before the study with an intensity of at least 3mm points on the visual analog scale (VAS).
排除标准
- •1. Infection, injury, or bleeding of the skin
- •surrounding the area for cupping therapy.
- •2. Neuropathy in the cervical spinal cord
- •3. Analgesic ingestion within 4 hours preceding
- •experiment.
- •4. Inclusion of ââ?¬Å?red flagsââ?¬? and nerve root
- •5. Consumption of coffee, tea, or any other
- •caffeinated beverage within 4 hours prior to
- •the baseline measurement. Also, no tobacco
- •products had been smoked for a minimum of 30
- •min before the baseline data were recorded.
- •6. Neck pain due to trauma or complex or severe
- •pathological conditions such as radiculopathy,
- •whiplash-associated disorders, headache/
- •dizziness related to neck pain, fracture,
- •tumor, infections, and systemic diseases.
- •7. If patients had undergone invasive treatments
- •within the last 4 weeks, surgery to the spine
- •within the last year, or had been treated with
- •corticosteroids or opiates.
- •8. If they have received dry cupping therapy or
- •any other treatment performed to the neck or
- •shoulder region within the 6 weeks before the
研究者
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