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临床试验/NCT07489014
NCT07489014Enrolling By Invitation不适用

Comparison of the Effects of Mulligan Joint Mobilization and Instrument-Assisted Soft Tissue Mobilization on Pain Intensity, Cervical Awareness, and Functionality in Individuals With Chronic Neck Pain

Istanbul Rumeli University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年3月13日最近更新:

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
40
试验地点
1
主要终点
Pain Intensity

研究概览

简要总结

The study will include a total of 40 individuals aged 18-65 years with chronic neck pain for at least three months. Participants will be randomly assigned to two groups: the Mulligan mobilization group (n=20) and the AYDM group (n=20). Both groups will receive a total of 12 treatment sessions, 3 days a week for 4 weeks. Assessments will be performed before and after treatment. Pain intensity will be assessed using the Visual Analog Scale (VAS), cervical awareness using the Fremantle Neck Awareness Questionnaire (FNA), and functionality using the Copenhagen Neck Functional Disability Scale (CNFDS). In addition, measurements of cervical joint range of motion, deep neck flexor muscle endurance, quality of life (SF-36), and depression level (Beck Depression Scale) will be taken.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • • Volunteering to participate in the study
  • Being between 18 and 65 years of age
  • Having experienced mechanical neck pain for at least 3 months
  • Not having any contraindications for manual therapy

排除标准

  • Receiving a diagnosis of a psychiatric illness
  • Having a history of spinal surgery
  • Having other musculoskeletal problems that may affect the cervical region (such as scoliosis, shoulder pathologies, thoracic outlet syndrome)
  • Having received physiotherapy for neck and back problems within the last year.

结局指标

主要结局

Pain Intensity

时间窗: Baseline and at the end of treatment (week 4)

Visual Pain Scale.Participants' pain intensity will be assessed using the Visual Analog Scale (VAS). The Visual Analog Scale is a validated and reliable scale that quantitatively determines the intensity of pain perceived by an individual. The scale consists of a 10 cm long horizontal or vertical line, with one end of the line defined as "0 = no pain" and the other end as "10 = unbearable pain".

Range of motion

时间窗: Baseline and at the end of treatment (week 4)

To assess the active range of motion of the cervical joint, the tape measure method described by Hsieh et al. (1986) was used. This method is reported to be a practical and reliable measurement tool for assessing cervical range of motion in clinical practice.

Cervical awareness

时间窗: Baseline and at the end of treatment (week 4)

Fremantle Neck Awareness Questionnaire

Copenhagen Neck Functional Disability Scale

时间窗: Baseline and at the end of treatment (week 4)

Neck Functional Disability is a 15-item questionnaire. Total score(0-30) indicate higher disability

次要结局

  • Neck flexor endurance(Baseline and at the end of treatment (week 4))
  • SF-36 Quality of life(Baseline and at the end of treatment (week 4))
  • Depression Scale(Baseline and at the end of treatment (week 4))

研究者

发起方
Istanbul Rumeli University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ozden Baskan

Doctor physiotherapist

Istanbul Rumeli University

研究点 (1)

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