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Effect of Neck and Upper Back Joint Therapy on Pain, Neck Movement, and Daily Activities in Computer Users with Upper Back Muscle Pain

The Effects of Cervicothoracic Mobilization on Pain, Cervical Side Flexion ROM and Functional Disability in Cervical Myofascial Pain Syndrome of Upper Trapezius Muscles in Computer Workers: A Randomized Controlled Trail - ROM - Range of motion

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105512
Enrollment
56
Registered
2026-03-06
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: M791- Myalgia

Interventions

Intervention1: Cervicothoracic Mobilisation + Conventional Treatment: Moist pack (application for 5-10 minutes in sitting position) Upper trapezius stretching (passive stretching given in sitting posi

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Diagnosis of trigger point in upper trapezius (Unilateral) according to criteria given by Simons et al 1983. a) A taut palpable band in the affected muscle. b) Exquisite focal tenderness to digital pressure (the trigger point), in the taut band of the muscle. c) A local twitch response, elicited through snapping palpation or needling of the tender spot. d) Reproduction of typical referred pain pattern of Trigger Point in response to compression. (Simons et al 1999) 2) Clinical presentation of unilateral upper trapezius shortness. 3) The ROM of the side contra lateral to presence of trigger point should be decreased than ipsilateral side.

Exclusion criteria

Exclusion criteria: 1) Any contraindication to manual therapy 2) Diagnosis of fibromyalgia syndrome according to American college of Rheumatology. 3) History of any surgery in cranio-cervical region 4) History of whiplash injury 5) Any diagnosed case of neurological/ Psychological/ psychiatric / dermatological/ deficit or disorders that can affect the study. 6) Participants who are not willing to participate or discontinue.

Design outcomes

Primary

MeasureTime frame
Visual Analogue ScaleTimepoint: At Baseline and after 4 weeks

Secondary

MeasureTime frame
cervical ROMTimepoint: pre and post treatment of 4 weeks;ain pressure threshold measure through syringe Algometer. (PPT)Timepoint: pre and post treatment of 4 weeks;Neck pain and disability scaleTimepoint: pre and post treatment of 4 weeks

Countries

India

Contacts

Public ContactDr Vaibhavi Walimbe

MGM School of Physiotherapy

vaibhavi181994@gmail.com7058271894

Outcome results

None listed

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