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Clinical Trials/NCT05860049
NCT05860049CompletedNot Applicable

Adding Instrument Assisted Soft Tissue Mobilization to Core Stability Training in Chronic Mechanical Neck Pain

Cairo University1 site in 1 country52 target enrollmentStarted: August 29, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
52
Locations
1
Primary Endpoint
Cervical range of motion and proprioception

Study Overview

Brief Summary

Purpose of the study was to investigate the effect of adding instrument assisted soft tissue mobilization to core stability training in treatment of chronic mechanical neck pain on pain level, cervical ROM, proprioception, muscle activity, H-reflex, and functions.

Detailed Description

Neck pain (NP) is a common musculoskeletal condition with a lifetime incidence rate between 22% and 70%.

Neck pain is commonly a recurrent condition with remissions and exacerbation that do not completely resolve. A history of previous injury to the neck (including whiplash, sports and work injuries etc.) increases the likelihood of chronic pain. As one ages, more chronic neck pain persists.

Mechanical neck pain is pain and/or stiffness in the neck or shoulder girdle region which was reproducible with neck movements.

Mechanical neck pain is the most common type found in neck-pain disorders. Studies have demonstrated altered behavior of the cervical muscles in mechanical neck-pain patients.

Mechanical neck pain produces mobility restriction, functional disability, decrease in muscle strength and decrease in health related quality of life.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients diagnosed as having chronic mechanical neck pain.
  • •Patient's age between 18-55 years old.

Exclusion Criteria

  • •Subjects with any specific neck pathology as radiculopathy, rheumatoid arthritis and systemic diseases.
  • •sensory problems at mid or upper back.
  • •A history of head and upper trunk trauma or surgery.
  • •severe disorders of the cervical spine such as disk prolapse and cervical stenosis.

Arms & Interventions

Conventional physiotherapy + Core stability

Active Comparator

They received conventional physical therapy and core stability for 4 weeks.

Intervention: Conventional physiotherapy (Other)

Conventional physiotherapy + Core stability

Active Comparator

They received conventional physical therapy and core stability for 4 weeks.

Intervention: Core stability (Other)

Conventional physiotherapy + Core stability + Instrument assisted soft tissue mobilization (IASTM)

Experimental

They received conventional physical therapy, core stability, and IASTM technique for 4 weeks.

Intervention: Instrument assisted soft tissue mobilization (Device)

Conventional physiotherapy + Core stability + Instrument assisted soft tissue mobilization (IASTM)

Experimental

They received conventional physical therapy, core stability, and IASTM technique for 4 weeks.

Intervention: Conventional physiotherapy (Other)

Conventional physiotherapy + Core stability + Instrument assisted soft tissue mobilization (IASTM)

Experimental

They received conventional physical therapy, core stability, and IASTM technique for 4 weeks.

Intervention: Core stability (Other)

Outcomes

Primary Outcomes

Cervical range of motion and proprioception

Time Frame: 4 weeks

Cervical range of motion and proprioception were measured using CROM.

Functions

Time Frame: 4 weeks

Functions were measured by Arabic version of Neck Disability Index. It is consisting of 10 items with six choices (0-5), Each item is scored from zero (no disability) to five (total disability). Minimum score means it is better.

H-reflex

Time Frame: 4 weeks

H-reflex was measured by EMG.

Pain level

Time Frame: 4 weeks

The pain level was measured by visual analogue scale.The VAS is a 100-mm horizontal line anchored by word descriptors at each end by ''no pain'' on the left and ''worst imaginable pain'' on the right. The minimum score means it is better.

Muscle activity

Time Frame: 4 weeks

Muscle activity was measured by electromyography (EMG).

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

RAGHDA MOHAMED HASSAN MAHMOUD

physical therapist

Cairo University

Study Sites (1)

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