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

Effective Quantification and Comparison among Dry Cupping, Scapulothoracic Mobilization, Foam Rolling in patients with Non-specific neck pain.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/01/039779
Enrollment
90
Registered
2022-01-28
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M799- Soft tissue disorder, unspecified

Interventions

Intervention1: GROUP 1- Dry Cupping therapy along with conventional Physical therapy.: CUPPING THERAPY It is done by the therapist. Patient position-prone lying with upper torso bared Area covered- ex

Sponsors

No sponsor
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
-Range Of Motion -Pain of Daily LivingTimepoint: Week 0, 2nd week, 4th week, follow-up after 2 weeks.—

Secondary

MeasureTime frame
DisabilityTimepoint: Week 0, 2nd week, 4th week, follow-up after 2 weeks—

Countries

India

Contacts

Public ContactKM NABA SULTANA

Amity institute of physiotherapy

naba.sultana@gmail.com9870873398

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026