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临床试验/NCT04872335
NCT04872335已完成不适用

Comparative Effects of Gong's Mobilization With Gradually Graded Exercise Therapy for Chronic Neck Pain Among the Electronic Gadgets Users.

Riphah International University4 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2020年10月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
28
试验地点
4
主要终点
Change in Pain Intensity by 'Numeric Pain Rating Scale'

研究概览

简要总结

This project was a Randomized clinical trial conducted to find out the Comparative Effects of Gong's Mobilization with Gradually Graded Exercise Therapy for Chronic Neck Pain among the users of Electronic Gadgets so that we can have best treatment option for patients.

详细描述

The study design was a Randomized Clinical Trial. For the study data was collected from sports and spine professionals. Sample size was calculated with the help of Epitool calculator. The study will be completed in 6 months duration. Neck Disability Index (NDI), Numeric Pain Rating Scale (NPRS) for pain intensity and Universal Goniometers for measuring (ROMs) and Forward head posture (FHP) were assessed before and 4 weeks after the treatment through the craniovertebral angle (CVA) measured from a digitized, lateral-view photograph of each subject. All the subjects were selected using Non Probability convenient sampling technique. The Subjects were randomly assigned to one of the following two groups: Gong's Mobilization (Group 1) or Gradually Graded Exercise Therapy (Group 2).This study was conducted in accordance with the rules of the Declaration of Helsinki. Written Informed consent were taken from all the subjects before participating in this trial. SPSS 25 was used for data entry and analysis.

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 (Participant)

入排标准

年龄范围
15 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects with an age range of 15 to 65 years having Chronic neck pain for more than 3 months and subjects having a baseline NDI score of atleast 20% (10 points).

排除标准

  • • Cervical stenosis
  • History of traumatic Injury
  • Previous surgery related to cervical spine
  • Hypermobility
  • Inflammatory rheumatologic diseases
  • Severe psychological disorders
  • Being pregnant and
  • Intervention including exercise or physical therapy in the last 3 months.

结局指标

主要结局

Change in Pain Intensity by 'Numeric Pain Rating Scale'

时间窗: Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week)

Change in pain from baseline was measured at 12th session. The Numerical Pain Rating Scale (NPRS) is an 11 point pain scale that is completed by subject himself, under the supervision of researcher.

Change in Neck disability Index 'NDI' score

时间窗: Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week)

Change in Neck disability Index score 'NDI' from baseline was measured at 12th session. This questionnaire or tool has been designed to give us information as to how neck pain of the subject has affected his/her ability to manage in everyday life.

次要结局

  • Change in Cervical Range of Motion (ROM) measured by Universal Goniometer.(Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week))
  • Change in Craniovertebral angle CVA measured from a digitized, lateral-view photograph of each subject.(Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rabiya Noor

Associate Professor

Riphah International University

研究点 (4)

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