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Mulligans SNAG Technique Versus Maitland’s in case of non-specific neck pain with reduced cervical rotation Among College Students.

Comparative Study On The Efficacy Of Mulligans SNAG Technique Versus Maitland’s Mobilization On Pain & Range of Motion In Case Of Non-specific Upper Cervical Neck Pain Among College Students. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073626
Enrollment
50
Registered
2024-09-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: M542- Cervicalgia

Interventions

Intervention1: Mulligan’s SNAG Technique: Mulligan’s manual technique All the participants will be given 8-10 minutes of moist heat therapy in a sitting position while leaning onto a couch, with moi

Sponsors

Prakash Pandey
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients having complaints of neck pain and neck restriction for more than 2 weeks will be included. Patients having reduced cervical rotation unilaterally or bilaterally of more than 8-10 degrees on a universal goniometer. Patients having a pain score of 2 or above in NPRS scale Evaluation. Exclusively college students will be included. Patients not involved in any other Physiotherapy Treatment were included. Patients willing to participate will be included. Patients who are able to follow commands and able to comprehend will be included.

Exclusion criteria

Exclusion criteria: Patients having any other orthopedic conditions around the cervical region will be excluded. Patients with recent or past surgery around the cervical or shoulder region will be excluded. Patients with any neurological impairment or disturbances will be excluded. Patients receiving any other Physiotherapy treatment will be excluded. Patients with any metabolic disease of bone and joints will be excluded. Patients with any tumor or metastasis will be excluded. Patients with any vascular disease will be excluded. Patients with congenital neck deformities will be excluded. Patients with hypersensitivity to skin will be excluded.

Design outcomes

Primary

MeasureTime frame
Numerical Pain Rating Scale Universal GoniometerTimepoint: 3 weeks

Secondary

MeasureTime frame
Numerical Pain rating scale Universal goniometerTimepoint: 2 weeks

Countries

India

Contacts

Public ContactDr Madhusudan Tiwari

Mahatma Gandhi University of medical sciences and Technology, Jaipur

principal.physiotherapy@mgumst.org8290964159

Outcome results

None listed

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