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The effect of scapular muscles release technique on the thickness of scapular and neck muscles in patients with nonspecific neck pain: A Randomized Clinical Controlled Trial

The effect of axioscapular muscles release technique on the thickness of axioscapular and neck stabilizer muscles in patients with nonspecific neck pain: A Randomized Clinical Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210524051386N1
Enrollment
30
Registered
2021-12-27
Start date
2022-01-10
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

Chronic nonspecific neck pain. Other chronic pain

Interventions

Intervention 1: intervention group: will be treated by routine physiotherapy and axioscapular muscle release technique, the routine physiotherapy including exercise therapy will be used as stretching

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: All patients whose nonspecific neck pain has been diagnosed by a neurosurgeon According to the physiotherapist, at least one active trigger point in the axioscapular muscles (upper trapezius and middle trapezius) Visual Analogue Scale of neck pain at least 3, maximum 7 Neck Disability Index at least 10, maximum 40 At least three months have passed since the onset of neck pain Normal Body Mass Index between 20 and 25

Exclusion criteria

Exclusion criteria: The patients with neurological symptoms and radiculopathy in their upper extremities Patients who have a pacemaker in the heart Patients with a history of surgery in the neck and scapula Patients who have a systemic rheumatic diseases Patients with congenital malformations in the neck and scapula Women who are pregnant Patients with a history of trauma in the neck and scapula Patients who have malignancy People who received scapular muscle release treatment 1 month before the study started

Design outcomes

Primary

MeasureTime frame
Thickness of upper trapezius, middle trapezius. Timepoint: Beginning of the study (before the intervention) and after the end of treatment sessions (10 sessions later). Method of measurement: sonography siemens healthineers - acuson juniper.;Cross sectional of longus colli, cervical multifidus. Timepoint: Beginning of the study (before the intervention) and after the end of treatment sessions (10 sessions later). Method of measurement: sonography siemens healthineers - acuson juniper.

Secondary

MeasureTime frame
Pain intensity. Timepoint: Beginning of the study (before the intervention) and after the end of treatment sessions (10 sessions later). Method of measurement: Visual Analogue Scale.;Pressure Pain Threshold. Timepoint: Beginning of the study (before the intervention) and after the end of treatment sessions (10 sessions later). Method of measurement: Digital Algometer.;Neck disability. Timepoint: Beginning of the study (before the intervention) and after the end of treatment sessions (10 sessions later). Method of measurement: Neck Disability Index Questionnaire (Iranian version).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBahram Amirshakri

Tabriz University of Medical Sciences

amirshakerib@tbzmed.ac.ir+98 41 3337 5359

Outcome results

None listed

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