跳至主要内容
临床试验/NCT07566637
NCT07566637已完成不适用

Low-Intensity Laser Therapy Versus Proprioceptive Neuromuscular Facilitation for Pain and Disability in Chronic Non-Specific Neck Pain: A Randomized Controlled Trial

Istanbul Gedik University1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2024年2月5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
75
试验地点
1

研究概览

简要总结

This study aimed to investigate and compare the effects of low-intensity laser therapy, a photobiomodulation treatment, and proprioceptive neuromuscular facilitation on pain and disability in individuals with non-specific neck pain. This randomized controlled trial used the Numerical Pain Scale (primary outcome) and the Bournemouth Neck Pain Questionnaire to assess pain, a manual algometer to assess pain threshold, and the Neck Disability Index to assess disability. Three groups were included in this randomized controlled trial: Group 1: Photobiomodulation therapy (low-intensity laser therapy) + conventional physiotherapy; Group 2: Proprioceptive neuromuscular facilitation with stretching and strengthening + conventional physiotherapy; Group 3: Conventional physiotherapy only. We hypothesized that low-intensity laser therapy and proprioceptive neuromuscular facilitation would have distinct effects on pain and disability in chronic non-specific 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
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
  • A neck pain score of at least 3 on the Numerical Pain Scale in the assessment conducted prior to inclusion in the study
  • A Neck Disability Index score of 5 or higher
  • No comorbid conditions affecting the orthopaedic, neurological or cardiopulmonary systems
  • Participants who have not been enrolled in another clinical trial within the last month

排除标准

  • Individuals who have undergone upper limb surgery (e.g. shoulder blade, shoulder, elbow, hand, wrist, etc.) within the last year
  • Individuals with a pacemaker or subcutaneous implant
  • Pregnant women or women who have recently given birth
  • Use of antidepressants, anti-inflammatory drugs or anxiolytics within the last 6 months

研究者

发起方
Istanbul Gedik University
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验