Muscle Energy Technique Versus Mulligan Mobilization on F... | NCT06732557

NCT06732557

Protocol Section

Identification Module

Results Section

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Annotation Section

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Document Section

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Derived Section

Miscellaneous Info Module

Status Module

Description Module

Design Module

Interventional Study Design

Biospecimen

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No data is available for this block.

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Group A: Control group (Traditional treament)	Sham Comparator	patients will receive traditional treatment (isometric exercise for deep neck flexors plus sub occipital release).	Other: Traditional treatments
Group B (muscle energy technique group)	Experimental	Patients will receive muscle energy Technique for upper trapezius, elevator scapulae and sternocleidomastoid	Other: Traditional treatments Other: muscle energy technique
Group C (Mulligan Mobilization Group)	Active Comparator	Patients will receive Mulligan mobilization	Other: Traditional treatments Other: Mulligan Mobilization

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Traditional treatments	Other	Isometric exercise for deep neck flexors and sub occipital release	Group A: Control group (Traditional treament) Group B (muscle energy technique group)

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Pain	Pain will be measured by visual analogue scale which is a valid and reliable scale for measuring pain starts with zero (represents no pain) and ends with 10 (represents maximum pain).	Before the first session and at the end of the treatment program ( one month)
Cervical range of motion	Cervical range of motion in will be measured by cervical range of motion basic assessment device (CROM) the angle of cervical range of motion will be recorded in degrees to determine the limitation in range of motion	Before the first session and after the end of the treatment program ( one month)
Disability measurement	Disability will be measured by neck disability index(NDI) is a valid and reliable scale. The NDI consists of ten questions in the following domains: Pain Intensity, Personal Care, Lifting, Reading, Headaches, Concentration, Work, Driving, Sleeping, and Recreation. Scoring: Each question contains six answer choices, scored from 0 (no disability) to 5 (complete disability). All section scores are then totaled. Scoring is reported on a 0-50 scale, 0 being the best possible score and 50 being the worst. Alternately, the score can be reported from 0-100. The score is often reported as a percentage (0-100%).	Before the first session and after the end of the treatment program ( one month)
Cervicovertebral angle	Cervicovertebral angle (CVA) Will be measure by kinovea: Normal range is between 55 and 86, If the angle is less than 50 degrees, it will be considered to be FHP. Adhesive markers (8 mm in diameter) will be placed on the participant's C7 spinous process and tragus of the ear. The physical therapist will observe the participant from the lateral side while standing and then take a picture of the participant from a fixed distance (75 cm) and height (150 cm), then with the help of an application sealed by a password which is called KINOVEA, the angle will be measured by placing each vector as following a line from the tragus of the ear to the C7 spinous process and another horizontal line through the C7 spinous. The angle will be recorded in degrees

Eligibility Module