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临床试验/NCT07761793
NCT07761793尚未招募不适用

Effect of Adding Diaphragmatic Myofascial Release to a Neck Exercise Program on Pain, Disability, Fatigue, and Kinesiophobia Among Patients With Chronic Neck Pain in the Gaza Strip: A Randomized Controlled Trial

Abdelrahman Alghoul1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年10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
发起方
入组人数
60
试验地点
1
主要终点
Change in Neck Disability Index (NDI) Score

研究概览

简要总结

Chronic neck pain can affect daily activities and may be associated with pain, disability, fear of movement, and fatigue. Exercise is commonly used to manage chronic neck pain, but some people continue to experience symptoms despite exercise treatment.

This study will investigate whether adding diaphragmatic myofascial release, a hands-on manual therapy directed toward the diaphragm and surrounding tissues, to a neck exercise program provides greater benefits than neck exercises alone in adults with chronic neck pain.

Sixty adults aged 25 to 60 years with chronic neck pain lasting more than three months will be randomly assigned to one of two groups. The control group will receive a supervised neck exercise program, while the intervention group will receive the same neck exercise program combined with diaphragmatic myofascial release and related diaphragmatic manual therapy. Both groups will receive treatment for six weeks, with three supervised sessions per week.

Pain, neck-related disability, fear of movement, and fatigue will be assessed before treatment, immediately after the six-week intervention, and four weeks after completion of treatment. The study will examine whether adding diaphragmatic myofascial release to neck exercises leads to greater improvements in these outcomes compared with neck exercises alone.

详细描述

This study is a prospective, assessor-blinded, parallel-group randomized controlled trial that will be conducted at the outpatient Physical Therapy Clinic of Nasser Medical Complex in the Gaza Strip. The study aims to evaluate the added effect of diaphragmatic myofascial release and diaphragm-directed manual therapy when combined with a standardized neck exercise program in adults with chronic neck pain.

Participants will be randomly allocated in a 1:1 ratio to either an intervention group or a control group using a computer-generated random sequence. The control group will receive a supervised neck exercise program that includes deep cervical flexor training, cervical stabilization, stretching, postural correction, scapular strengthening, and a home exercise program. The intervention group will receive the same neck exercise program in addition to a diaphragm-focused intervention that includes manual diaphragm release, diaphragmatic myofascial release, release of accessory respiratory muscles, and breathing re-education.

The intervention period will last six weeks, with three supervised treatment sessions per week. Outcomes will be assessed at baseline, immediately after the intervention, and at a four-week follow-up. The clinical outcomes include neck-related disability measured using the Neck Disability Index (NDI), pain intensity measured using the Numeric Pain Rating Scale (NPRS), kinesiophobia measured using the Tampa Scale of Kinesiophobia (TSK-17), and fatigue measured using the Fatigue Severity Scale (FSS).

The study will compare changes over time between the intervention and control groups to determine whether adding the diaphragmatic intervention to neck exercises provides additional benefits for patients with chronic neck pain.

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
25 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Men and women aged 25-60 years.
  • •Diagnosis of chronic neck pain lasting longer than 3 months.
  • •Ability to understand and follow instructions.

排除标准

  • •Previous cervical spine surgery.
  • •Cervical radiculopathy or myelopathy.
  • •History of fracture, inflammatory disease, malignancy, or neurological disorder.
  • •Respiratory diseases such as chronic obstructive pulmonary disease (COPD) or severe asthma.
  • •Current vestibular disorder.
  • •Pregnancy.
  • •Receipt of physical therapy or manual therapy during the previous 3 months.

研究组 & 干预措施

Neck Exercise Program

Active Comparator

Participants will receive a supervised neck exercise program consisting of deep cervical flexor training, cervical stabilization exercises, stretching exercises, postural correction, scapular strengthening, and a home exercise program. The intervention will be provided for 6 weeks with 3 supervised sessions per week.

干预措施: Neck Exercise Program (Other)

Neck Exercise Program + Diaphragmatic Intervention

Experimental

Participants will receive the same supervised neck exercise program as the active comparator group, combined with a diaphragm-focused intervention consisting of manual diaphragm release, diaphragmatic myofascial release, release of accessory respiratory muscles, and breathing re-education. Treatment will be provided for 6 weeks with 3 supervised sessions per week.

干预措施: Neck Exercise Program (Other)

Neck Exercise Program + Diaphragmatic Intervention

Experimental

Participants will receive the same supervised neck exercise program as the active comparator group, combined with a diaphragm-focused intervention consisting of manual diaphragm release, diaphragmatic myofascial release, release of accessory respiratory muscles, and breathing re-education. Treatment will be provided for 6 weeks with 3 supervised sessions per week.

干预措施: Diaphragmatic Myofascial Release and Diaphragm-Directed Manual Therapy (Other)

结局指标

主要结局

Change in Neck Disability Index (NDI) Score

时间窗: Baseline, immediately after the 6-week intervention, and 4 weeks after completion of the intervention

Neck-related disability will be assessed using the Neck Disability Index (NDI), a 10-item self-reported questionnaire assessing the impact of neck pain on daily functioning. Each item is scored from 0 to 5, producing a total score from 0 to 50, which can be expressed as a percentage from 0% to 100%. Higher scores indicate greater neck-related disability.

Change in Neck Disability Index (NDI) Score

时间窗: Baseline, immediately after the 6-week intervention, and 4 weeks after completion of the intervention.

Neck-related disability will be assessed using the Neck Disability Index (NDI), a 10-item self-reported questionnaire assessing the impact of neck pain on daily functioning. Each item is scored from 0 to 5, producing a total score from 0 to 50, which can be expressed as a percentage from 0% to 100%. Higher scores indicate greater neck-related disability.

次要结局

  • Change in Tampa Scale of Kinesiophobia (TSK-17) Score(Baseline, immediately after the 6-week intervention, and 4 weeks after completion of the intervention.)
  • Change in Numeric Pain Rating Scale (NPRS) Score(Baseline, immediately after the 6-week intervention, and 4 weeks after completion of the intervention)
  • Change in Fatigue Severity Scale (FSS) Score(Baseline, immediately after the 6-week intervention, and 4 weeks after completion of the intervention.)

研究者

发起方
Abdelrahman Alghoul
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Abdelrahman Alghoul

Master's Researcher in Physical Therapy

Al-Azhar University - Gaza

研究点 (1)

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