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临床试验/NCT07838623
NCT07838623招募中不适用

Comparison Between Kaltenborn and Mulligan Mobilization in Forward Head Posture

Foundation University Islamabad1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2026年7月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
44
试验地点
1
主要终点
Cervical Pain

研究概览

简要总结

This randomized controlled trial will compare the effectiveness of Kaltenborn mobilization and Mulligan mobilization in individuals with Forward Head Posture.

The study will compare their effects in neck pain, craniovertebral angle, cervical range of motion, cervical proprioception, and deep neck flexor endurance after a two-week treatment program.

详细描述

Participants aged 18-40 years will be recruited and randomly allocated into two groups of through purposive sampling. Group A will receive Kaltenborn mobilization, progressing from Grades I-II to Grade III, while Group B will receive Mulligan SNAGs with gradually increased repetitions and overpressure. Both groups will also receive conventional treatment three times weekly for two weeks, completing six sessions with progression according to symptoms and tolerance.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Both male and female
  • •aged between 18 to 40 years
  • •CVA of <48
  • •Pain on NPRS 3-8
  • •Hypo-mobility of cervical spine
  • •Joint Position Error > 4.5 in any of the cervical range
  • •Participants who gave consent

排除标准

  • •Acute musculoskeletal injuries of the cervical spine and shoulder in the last 6 months
  • •Diagnosed cases of pathological conditions like spondylosis, cervical myelopathy
  • •Whiplash injury of cervical spine in last 6 months
  • •Neck and shoulder surgery
  • •Diagnosed cases of osteoporosis
  • •Rheumatoid arthritis
  • •Uncontrolled diabetes and hypertension

研究组 & 干预措施

Kaltenborn mobilization group

Experimental

干预措施: Kaltenborn mobilization (Procedure)

Mulligan mobilization group

Experimental

干预措施: Mulligan Mobilization (Procedure)

结局指标

主要结局

Cervical Pain

时间窗: Baseline and after 2 weeks of treatment.

Numeric Pain Rating Scale (NPRS) will be used to measure Pain, 0 means no pain and 10 means worst pain ever.

Cervical Range of Motion

时间窗: Baseline and after 2 weeks of treatment

A bubble inclinometer will be used to measure cervical range of motion.

CranioVertebral Angle

时间窗: baseline and after 2 weeks of treatment.

Kinovea software will be used to measure Craniovertebral Angle.

Cervical Joint Proprioception

时间窗: Baseline and after 2 weeks of treatment

Cervical Joint Proprioception will be measured via Joint position error test.

Deep Neck Flexor Muscle Endurance

时间窗: Baseline and after 2 weeks of treatment

Deep Neck Flexor Muscle Endurance will be measured by Deep Neck Flexor Muscle Endurance test.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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