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临床试验/NCT06732557
NCT06732557尚未招募不适用

Muscle Energy Technique Versus Mulligan Mobilization on Forward Head Posture: a Randomized Controlled Trial

Cairo University0 个研究点目标入组 60 人开始时间: 2024年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
主要终点
Pain

研究概览

简要总结

sixty patients with forward head posture will be randomized to three groups Group A: will receive traditional treatment ( isometric exercise for deep neck flexors plus sub occipital release).

Group B: will receive traditional treatment plus muscle energy technique for upper trapezius, elevator scapulae and sternocleidomastoid.

Group C: will receive traditional treatment plus mulligan mobilization

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age between 18 to 45 years
  • •Non specific neck pain reproduced by neck movement
  • •Neck pain at least within the last three months
  • •Limitation in cervical range of motion

排除标准

  • •cervical spine surgery or injury
  • •neurologic deficits, infection or inflammation
  • •cervicogenic headache

研究组 & 干预措施

Group C (Mulligan Mobilization Group)

Active Comparator

Patients will receive Mulligan mobilization

干预措施: Traditional treatments (Other)

Group A: Control group (Traditional treament)

Sham Comparator

patients will receive traditional treatment (isometric exercise for deep neck flexors plus sub occipital release).

干预措施: Traditional treatments (Other)

Group B (muscle energy technique group)

Experimental

Patients will receive muscle energy Technique for upper trapezius, elevator scapulae and sternocleidomastoid

干预措施: Traditional treatments (Other)

Group B (muscle energy technique group)

Experimental

Patients will receive muscle energy Technique for upper trapezius, elevator scapulae and sternocleidomastoid

干预措施: muscle energy technique (Other)

Group C (Mulligan Mobilization Group)

Active Comparator

Patients will receive Mulligan mobilization

干预措施: Mulligan Mobilization (Other)

结局指标

主要结局

Pain

时间窗: Before the first session and at the end of the treatment program ( one month)

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).

Cervical range of motion

时间窗: Before the first session and after the end of the treatment program ( one month)

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

Disability measurement

时间窗: Before the first session and after the end of the treatment program ( one month)

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%).

Cervicovertebral angle

时间窗: Before the first session and after the end of the treatment program ( one month)

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

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mariam Nazih Radwan Meshref

teaching assistant of Basic Science Department

Cairo University

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