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临床试验/NCT06440720
NCT06440720进行中(未招募)不适用

COMPARATIVE EFFECTS OF ELONGATION LONGITUDINAUX AVEC DECOAPTION OSTEO ARTICULAIRE VERSUS UPPER THORACIC MOBILIZATION AND MOBILITY EXERCISE FOR THE TREATMENT OF FORWARD HEAD POSTURES

University of Faisalabad2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2024年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
36
试验地点
2
主要终点
Craniovertebral angle

研究概览

简要总结

This study will compare the effectiveness of the Elongation Longitudinaux Avec Decoaptation Osteo Articulaire (ELDOA) method and upper thoracic mobilization and mobility exercises in correcting forward head posture (FHP). This study aims to evaluate the effectiveness of these methods in reducing forward head posture. The total sample size will be 36, with each group consisting of 18 participants. This study will be a randomized clinical trial. Participants who meet the inclusion criteria will be selected through screening and then assessed for outcomes using NPRS, a goniometer, the Neck Disability Index (NDI), and Web Plot Digitizer (WPD) Software. Statistical analysis will be conducted using SPSS version 27.

详细描述

Study Title Comparative Effectiveness of the ELDOA Method and Upper Thoracic Mobilization and Mobility Exercises in Correcting Forward Head Posture: A Randomized Clinical Trial

Introduction Forward Head Posture (FHP) is a common postural deformity characterized by an anterior positioning of the head relative to the vertical axis of the body. This condition can lead to various musculoskeletal issues, including neck pain, reduced range of motion, and increased disability. The Elongation Longitudinaux Avec Decoaptation Osteo Articulaire (ELDOA) method and upper thoracic mobilization and mobility exercises are two interventions aimed at correcting FHP. This study aims to compare the effectiveness of these two methods in reducing FHP and associated symptoms.

Objectives The primary objective of this study is to evaluate and compare the effectiveness of the ELDOA method and upper thoracic mobilization and mobility exercises in reducing FHP. Secondary objectives include assessing improvements in pain levels, neck disability, and range of motion.

Study Design This study is a randomized clinical trial.

Participants A total of 36 participants will be recruited and randomly assigned to one of two intervention groups, each consisting of 18 participants.

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
None

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Both males and females.
  • Age between 20 to 40 years.
  • Patients having complain of neck pain
  • Patients having forward head posture
  • Patients having limited Cervical range of motion
  • Patients having Craniovertebral angle CVA less than
  • Pain more than 3 on NPRS scale with FHP

排除标准

  • History of whiplash injury within 3 months of examination.
  • History of tumor
  • History of surgery of cervical or thoracic spine.
  • Positive neurological signs
  • Congenital deformity
  • Patients having pathology and infection in spine.
  • Patients having severe osteoporosis

结局指标

主要结局

Craniovertebral angle

时间窗: 5 Minutes

The primary outcome measure was the CVA, which was calculated using each participant's profile photo. The self-balanced posture assessment method was used to force the participants to maintain their typical head posture. By drawing a vertical line from Targus to the seventh cervical vertebrae and a horizontal line across them, the angle between them may be calculated to determine the CVA angle. The CVA measurement was shown to have excellent reliability in a prior research.

次要结局

  • Neck disability Index(10 minutes)
  • Numeric Pain Rating Scale(5 Minutes)
  • Cervical ranges of motion(20 Minutes)

研究者

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

Faiza Khalid

FAIZA KHALID

University of Faisalabad

研究点 (2)

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