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Effects of integrated neuromuscular inhibition technique on upper trapezius trigger points in patients with non specific neck pain

Effects of integrated neuromuscular inhibition technique on upper trapezius trigger points in patients with non specific neck pain: a randomized controlled trail

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220104053617N1
Enrollment
48
Registered
2022-03-23
Start date
2021-12-24
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Non specific neck pain. Panniculitis affecting regions of neck and back, cervical region

Interventions

Intervention 1: Control group:this group will receive training in 30-minute sessions, 5times per week, for 8 weeks. Total duration of treatment in this group will be 30 minutes. Thirty minutes for con

Sponsors

University of Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Subjects suffering from non-specific neck pain, defined as non-articular or non-systemic as per the referring physician. Subjects will be required to have neck pain of less than 3 months duration as well as active TrPs inthe upper trapezius muscle, defined as a tender nodule in a taut band that referred pain beyondthe area of contact

Exclusion criteria

Exclusion criteria: If patiant with neck symptoms will be related to a motor vehicle collision or significant trauma, they will not be included in our study If patiants will be presenting with signs of serious pathology (e.g. malignancy, infection, inflammatorydisorder, or fracture), then he/she will not be included in the trial Patients with signs of cervical spinal cord compromise (e.g. diffuse sensory abnormality, diffuse weakness, hyperreflexia, or the presence of clonus), two or more signs of nerve rootinvolvement (e.g. dermatomal sensation changes, myotomal weakness, or diminished/absenttendon jerk reflexes) A history of neck surgery during the previous 12 months, and a history of cervical degenerativejoint disease as per radiographs, endocrine disorders, and autoimmune conditions (e.g. rheumatoid arthritis, fibromyalgia, etc.) If pateints had received trigger point injections in the upper trapezius muscle within the past 6 months, they will not be included in our study

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Pain will be assessed at Baseline and after every week for 4 weeks. Method of measurement: Visual Analog Scale will be utilized for the assessment of pain.;Functional disability. Timepoint: Functional Disability will be assessed at Baseline and after every week for 4 weeks. Method of measurement: Neck Disability Index will be utilized for this purpose.

Countries

Pakistan

Contacts

Public ContactNusrat Qamar

University of Lahore

dr.nusratqamar55@gmail.com092 021 111 844 844

Outcome results

None listed

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