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Effects of Cervical and Oculomotor Exercises in Young Adults With Benign Paroxysmal Positional Vertigo

2026年5月8日 更新者：Foundation University Islamabad
Benign paroxysmal positional vertigo (BPPV) is the most common type of dizziness disorder in the community.Its cardinal symptoms include vertigo which is induced by change in position of head, turning over in bed, looking up, lying down in bed or any sudden change in the position of head. This study compares the effectiveness of occulomotor exercises alone and combined cervical and occulomotor exercises which take 6 weeks to implement and recruit results and each session lasting 10-20 minute Assessment will be performed at baseline.

研究概览

地位

完全的

条件

干预/治疗

详细说明

Benign Paroxysmal Positional Vertigo (BPPV) is the most prevalent peripheral vestibular disorder, significantly affecting patients' daily activities and quality of life. While vestibular maneuvers are widely used for treatment, evidence on the added benefits of combining these maneuvers with therapeutic exercises remains limited. This study aims to fill that gap by evaluating the effectiveness of an integrated approach, potentially enhancing symptom relief and supporting evidence-based clinical decisions. The combination may offer a more holistic strategy for managing BPPV, guiding healthcare professionals toward improved treatment protocols. Additionally, the research emphasizes a quick, accessible intervention suitable for clinical and emergency settings. By reducing dizziness more effectively, the study aspires to improve functional outcomes for patients. Overall, it highlights the value of innovative, combined therapies in vestibular care.

研究类型

介入性

注册 (实际的)

56

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。

学习地点

  • 巴基斯坦
      • Islamabad、巴基斯坦、44000
        • Foundation University College of Physical Therapy

参与标准

研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

  • Diagnosed Patients of Benign Paroxysmal Vertigo (BPPV)
  • Age between 18-35 years
  • Male & Female Patients
  • Positive Dix-Hall pike Test
  • Normal Cognitive Function: Able to follow instructions and provide informed consent.
  • Normal or Corrected-to-normal Vision
  • DHI Scale: Moderate (0-100)

Exclusion Criteria:

  • Patients with visual impairment
  • Pregnancy
  • Patients with a history of severe heart disease
  • Patients with a pacemaker or implantable cardioverter-defibrillator (ICD)
  • No other vestibular disorders or conditions that may affect balance
  • Pre-Existing Neurological or Musculoskeletal Conditions

学习计划

本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。

研究是如何设计的？

设计细节

  • 主要用途：治疗
  • 分配：随机化
  • 介入模型：并行分配
  • 屏蔽：无（打开标签）

武器和干预

参与者组/臂
干预/治疗
实验性的：Cervical exercises
Week 1: DNF Strengthening (basic chin tuck) + Smooth Pursuit + Basic Saccades Week 2: DNF Progression (longer hold) + Saccadic Eye Movement + Smooth Pursuit Week 3: Adaptation X1 (with head movement) Week 4: DNF with Arm Movements + Adaptation X2 (slow head & target) Week 5: Saccades with Head Movements Week 6: DNF
程序：Cervical Exercises

Cervical exercise include Deep Neck flexor strengthening starts with the patient lie supine with knees bent.

Perform chin tuck and lift head ~2-3 cm off the surface. Hold for 5- 10 seconds. 10 repetitions, 2 sets daily.

DNF activate stabilizing neck muscles and reduce Cervicogenic Input & provides quick, non-invasive relief from BPPV.
实验性的：Occulomotor exercises
Week 1: Smooth Pursuit + Basic Saccades Week 2: Saccadic Eye Movement + Adaptation X1 (slow speed) Week 3: Adaptation X1 (moderate speed) + Smooth Pursuit (increased range) Week 4: Adaptation X2 (slow) + Complex Saccades (with distractions) Week 5: Adaptation X2 (faster) + Smooth Pursuit (large range) Week 6: All Oculomotor Exercises in Circuit (Saccades + Pursuit + X1 + X2)
程序：Occulomotor exercises

Oculomotor exercises are used to treat BPPV and involve repeated head movements to habituate the brain to vertigo triggers.

Saccadic Eye Movement Exercises: Moving the eyes quickly between two stationary targets while keeping the head still.

Smooth Pursuit Exercises: Tracking a moving target with the eyes while keeping the head stationary.

Adaptation X1 Exercises: Moving the head horizontally while maintaining focus on a stationary target.

Adaptation X2 Exercises: Simultaneously moving the head and target in opposite directions horizontally, requiring the eyes to track the moving target.

研究衡量的是什么？

主要结果指标

结果测量
措施说明
大体时间
Nystagmus
大体时间：6 weeks

Dynamic leap and balance test

Moderate Impairment:

Noticeable instability, excessive sway, needs extra steps to regain balance, and slower performance.

Severe Impairment:

Unable to maintain balance after landing, requires assistance, or is unable to complete the task safely.
6 weeks
benign paroxysmal positional vertigo
大体时间：6 weeks

Dix-Hall pike Test (DHT) is considered the gold standard assessment for the diagnosis of the vestibular disorder benign paroxysmal positional vertigo (BPPV).

The patient starts in a sitting position and their head is turned 45° towards the side to be tested. The assessor then assists them to lie down quickly and extends their neck 20° over the end of the plinth, maintaining 45° rotation. The assessor should be able to see the patient's eyes and should observe for nystagmus. A positive response is elicited if rotational nystagmus is noted. The nystagmus will have a delayed onset of approximately 1-2 seconds following movement and it should subside after 10-20 seconds
6 weeks
Dizziiness
大体时间：6 weeks
The Dizziness Handicap Inventory (DHI) is a widely used tool to assess the impact of dizziness on an individual's daily life.The total score ranges from 0 to 100, with higher scores indicating a greater impact of dizziness.
6 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

Foundation University Islamabad

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年2月20日

初级完成 (实际的)

2026年4月25日

研究完成 (实际的)

2026年5月1日

研究注册日期

首次提交

2026年5月8日

首先提交符合 QC 标准的

2026年5月8日

首次发布 (实际的)

2026年5月14日

研究记录更新

最后更新发布 (实际的)

2026年5月14日

上次提交的符合 QC 标准的更新

2026年5月8日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

关键字

其他相关的 MeSH 术语

其他研究编号

  • FUI/FUCP/CTR/Neuro/Anosha

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.

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