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Comparison of two physiotherapy interventions for non-specific neck pain

Comparative Effectiveness of Instrument-Assisted Soft Tissue Mobilization and Exracorporeal Shock Wave Therapy in Non-Specific Neck Pain: A Randomized Controlled Trial - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/07/113917
Enrollment
105
Registered
2026-07-14
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Health Condition 1: M95-M95- Other disorders of the musculoskeletal system and connective tissue

Interventions

Intervention1: Instrument-Assisted Soft Tissue Mobilization along with Ultrasound Therapy: The IASTM group (n=35) will receive approximately 3 minutes of IASTM treatment after identifying trigger poin

Sponsors

Sanhita Sengupta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: College students with myofascial trigger points in the upper trapezius muscle. Eligibility requires the presence of taut band, point tenderness at specific site, and reproduction of pain on examination. Additional findings may include referred pain, twitch response, and reduced range of motion

Exclusion criteria

Exclusion criteria: Malignancy, Cervical spine fractures, Cervical radiculopathy and myelopathy, whether they are undergoing any other treatments, such as physical therapy or medication, that could interfere with the results of this study, and any contraindications for IASTM, or ESWT

Design outcomes

Primary

MeasureTime frame
Pain Intensity will measured using Numerical Pain Rating Scale, and Pressure Pain Threshold will be measured using Pressure AlgometerTimepoint: Primary outcome measure will be recorded at thge baseline and after treatment completion after 2 weeks

Secondary

MeasureTime frame
Cervical Range of motion for flexion, extension, lateral flexion, & rotation will be measured using Bubble InclinometerTimepoint: Cervical range of motion will be recorded at the baseline & after treatment completion at 2 weeks;Functional limitations will be measured using Neck Disability IndexTimepoint: Functional limitations will be recorded at the baseline & after treatment completion at 2 weeks

Countries

India

Contacts

Public ContactSanhita Sengupta

Teerthenker Mahaveer University

dr.naveen.s@gmail.com9634895624

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026