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Effect Of Soft Tissue Mobilisation In Non Specific Chronic Neck Pain

Efficacy Of Instrument Assisted Soft Mobilisation Over Myofascial Release Technique In Individuals With Non Specific Chronic Neck Pain - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080603
Enrollment
66
Registered
2025-02-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue Health Condition 2: M709- Unspecified soft tissue disorder related to use, overuse and pressure

Interventions

Intervention1: Instrument Assisted Soft Tissue Mobilisation : Subjects in this group receive the Instrument Assisted Soft Tissue Mobilisation technique using an M2T blade twice a week for four week

Sponsors

Mohanasundaram K
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosis Nonspecific chronic neck pain lasting at least 12 weeks without a specific pathological cause. Age Range 18 60 years. Pain Intensity Moderate pain (VAS score: 3 7 out of 10). Functional Impairment Functional limitations in daily activities due to neck pain, assessed by the Neck Disability Index (NDI). Trigger Points Presence of active or latent myofascial trigger points (MTrPs) identified by clinical palpation.

Exclusion criteria

Exclusion criteria: Specific Neck Pain Neck pain caused by specific conditions (e.g., cervical radiculopathy, myelopathy, fractures, systemic inflammatory conditions). Neurological Disorders Presence of nerve root compression signs (e.g., numbness, tingling, or muscle weakness). Recent Surgery/Trauma History of neck or upper limb surgery or acute trauma within the last 6 months.

Design outcomes

Primary

MeasureTime frame
Pain intensity(VAS) Timepoint: Baseline and 4 weeks

Secondary

MeasureTime frame
pain pressure threshold Timepoint: Baseline & 4 weeks;endurance Timepoint: Baseline & 4 weeks;cervical range of motionTimepoint: Baseline & 4 weeks

Countries

India

Contacts

Public ContactAngeline R

Sri Ramachandra Institute of Higher Education and Research

angelinejobin.75@gmail.com9943529400

Outcome results

None listed

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