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Comparative effectiveness among Dry Cupping, Scapulothoracic Mobilization, Foam Rolling in patients with Non-specific neck pain.

Not Applicable
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
Inclusion Criteria

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).

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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