Comparative effectiveness among Dry Cupping, Scapulothoracic Mobilization, Foam Rolling in patients with Non-specific neck pain.
- Conditions
- Health Condition 1: M799- Soft tissue disorder, unspecified
- Registration Number
- CTRI/2022/01/039779
- Lead Sponsor
- o sponsor
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
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).
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
disorders
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
study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method