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临床试验/NCT07132047
NCT07132047已完成不适用

Mulligan Mobilization Sustained Natural Apophyseal Glide Versus Active Release Technique in Cervicogenic Headache

University of Lahore1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2025年7月1日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
72
试验地点
1
主要终点
Neck Disability Index (NDI) score

研究概览

简要总结

This study is designed to compare two different manual therapy approaches for individuals with cervicogenic headaches, a type of headache that originates from the neck. Participants will be randomly assigned to one of two groups.

The first group will receive Mulligan mobilization using sustained natural apophyseal glides (SNAG) along with a home program of Mobilization self-SNAG exercises.

The second group will receive the Active Release Technique (ART) combined with a home program of stretching and strengthening exercises for the neck and shoulder muscles. Each participant will attend treatment sessions three times per week for four weeks. Pain levels, headache impact, and neck function will be evaluated at the start, after four weeks of treatment, and again at eight weeks to determine which method provides better outcomes.

详细描述

Cervicogenic headache is a form of secondary headache caused by dysfunction in the cervical spine. It is often associated with neck pain, restricted mobility, and limitations in daily activities. Manual therapy, combined with targeted exercises, is frequently used in rehabilitation to reduce pain and improve neck function. This randomized controlled trial aims to compare the effectiveness of Mulligan mobilization with sustained natural apophyseal glides (SNAG) versus the Active Release Technique (ART) in the treatment of cervicogenic headache.

Group A - Mulligan Mobilization SNAG and Home Exercise:

Participants in this group will receive the Headache SNAG technique, which involves a gentle, sustained postero-anterior glide of the second cervical vertebra for 10 to 30 seconds to help reduce headache intensity. If relief is noted, up to six repetitions may be performed. In addition, each participant will be prescribed a home program consisting of C1-C2 self-SNAG rotation using a towel to apply pressure on the posterior arch of C1 during active cervical rotation. The exercise will be completed twice daily, with 10 repetitions per session. Written instructions will be given to ensure correct performance and better compliance.

Group B - Active Release Technique and Home Exercise Program:

Participants allocated to this group will receive the Active Release Technique (ART), a hands-on treatment aimed at releasing tight muscles and improving soft tissue mobility. During ART, controlled pressure is applied to specific muscles while the neck is moved to restore normal function and reduce discomfort. Target muscles include the pectoralis major, upper trapezius, levator scapulae, rhomboids, deep neck flexors, and serratus anterior.

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
20 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • * Aged between 20-50 years
  • Both Male and females
  • Individuals diagnosed with neck pain accompanied by headaches.
  • Individuals with Unilateral or Bilateral cervicogenic headache.
  • Headache at least 3 times during the last 3 months.

排除标准

  • * History of inflammatory disorders (e.g Rheumatoid Arthritis).
  • History of trauma to the cervical region.
  • History of Neurological conditions (myelopathy, radiculopathy or disc problems).
  • Taking medications for headache.
  • Pregnancy.

结局指标

主要结局

Neck Disability Index (NDI) score

时间窗: Baseline, 4 weeks, and 8 weeks after start of intervention

The purpose of the Neck Disability Index (NDI) questionnaire is to gather data on how your neck pain has impacted your capacity to function in daily life. The NDI is divided into ten categories, each of which is rated from 0 to 5, where 5 represents "worst imaginable pain" and 0 represents "no pain". The sum of the points determines the final score, with 0 denoting no activity constraints and 50, or 100%, denoting entire activity limitations.

次要结局

  • Numeric Pain Rating Scale (NPRS) score.(Baseline, 4 weeks, and 8 weeks after start of intervention)
  • Headache Disability Index (HDI) score(Baseline, 4 weeks, and 8 weeks after start of intervention)

研究者

发起方
University of Lahore
申办方类型
Other
责任方
Sponsor

研究点 (1)

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