Sustained Natural Apophysial Glide Versus Instrument Assisted Soft Tissue Mobilization in Patients With Chronic Mechanical Neck Pain

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-55
SponsorCairo University

About this trial

this study will be conducted to investigate the effect of sustained natural apophysial glide and Instrument assisted soft tissue mobilization on pain intensity, cervical range of motion and neck functional disability level in patients with chronic mechanical neck pain

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Sixety patients of chronic mechanical neck pain diagnosed and reffered from physicians will be participants in the study .

Patients of both genders will be included.

The age of the participants will beranged from 20 and 55 years

The BMI ranged between 18.9 and 25 kg/m2

Disqualifiers

Malignancy

cervical and cranial surgery

Recent fractures

spinal tumors

Trial design

Design model

Parallel

Treatments tested in this trial

  • sustained natural apophysial glide

    Other intervention

    The patients will be in the sitting position and asked to move their head in the direction that particularly produces their symptoms. As the participant moves their head, the physiotherapist gently glides the painful vertebra anteriorly and sustains the glide through the movement. During the application of the glide, the participant should stay symptom free and is instructed to stop moving if any PAIN is produced. This movement was repeated for 10 times for 3 sets, The interval between the sets was 15 to 20 seconds.After mobilization subject had to perform same exercises as conventional group plus conventional physical therapy

  • instrument assisted soft tissue mobilization

    Other intervention

    The subject will be in comfortable sitting position leaning on a treatment table with the arm crossed to rest the head. After cleaning the skin of the subject and the blade with alcohol swabs, a lubricant (Vaseline) was applied, and a sweeping technique was used to apply a deep yet comfortable soft tissue mobilization on the upper trapezius from origin to insertion for approximately 3 min. First, M2T blade will be utilized to locate the precise locations of limitation in the affected muscles. Second, the M2T blade was put at 45 degree angle by using convex surface to apply gentle strokes along the muscle. Subjects were instructed that slight hyperemia on the skin is a normal feeling and should subside before the next session.

  • conventional physical therapy

    Other intervention

    the patients will receive conventional physical therapy in the form of Infrared, TENS , stretching exercices, isometric exercises

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: sustained natural apophysial glideExperimental treatment 2 interventions
Group B: instrument assisted soft tissue mobilizationExperimental treatment 2 interventions
Group C: conventional therapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

neck disability

Assessment of neck disability will be performed by Arabic version of neck disability index .It is valid and reliable tool in the assessment of neck function. The NDI can be calculated as a raw score or as a percentage Each segment is graded on a scale of 0 to 5, with 0 representing "no discomfort" and 5 suggesting "the most excruciating pain imaginable." With a maximum score of 50 as following

Time frame
up to four weeks

Secondary outcomes

1

pain intensity

pain intensity will be measured by visual analogue scale. It is a 10-cm (100-mm) line; with 0 refer to no pain while 100mm refer to extreme pain. Patients were requested to place a mark along the line to express their level of pain. The reliability VAS is moderate to good in subjects with musculoskeletal conditions.

Time frame
up to four weeks
2

cervical range of motion

cervical range of motion device will be used to measure the neck ROM for flexion, extension, rotations, and lateral flexion using 3 separate inclinometers which are attached to a plastic frame and secured to the head by Velcro strap and nose bridge. The sagittal plane inclinometer measures flexion - extension, the frontal plane inclinometer measures right and left lateral flexion, and the horizontal plane inclinometer with a magnetic neck collar measures right and left rotation.

Time frame
up to four weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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