Actively Recruiting

Phase Not Applicable
Age: 20Years - 65Years
All Genders
ID06625281

Effects of Epleys Maneuver Versus Semont-Plus Maneuver Combined with Brandt-Daroff Exercises on Dizziness and Quality of Life in Benign Paroxysmal Positional Vertigo

Led by Foundation University Islamabad · Updated on 2024-10-03

40

Participants Needed

1

Research Sites

2 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Dizziness and balance problems caused by vestibular hypofunction, such as benign paroxysmal positional vertigo (BPPV), can significantly affect a person's quality of life and daily activities. This trial focuses on comparing two treatments for posterior canal BPPV: Epley's maneuver combined with Brandt-Daroff exercises, and the Semont-Plus maneuver combined with Brandt-Daroff exercises. The study aims to assess which treatment better improves dizziness and quality of life in affected individuals. Participants diagnosed with posterior canal BPPV will be randomly assigned to one of two groups. One group will receive Epley's maneuver along with Brandt-Daroff exercises, while the other will receive the Semont-Plus maneuver combined with the same exercises. Both groups will undergo their assigned treatment for six weeks. These maneuvers involve specific head and body movements performed by therapists to help reposition ear crystals, and the exercises are designed to reduce dizziness symptoms. Participants will have their dizziness and quality of life measured at the start of the study and again after the six-week treatment period using the Dizziness Handicap Inventory and the Vestibular Activities and Participation measure. The study includes baseline assessments, treatment sessions, and follow-up evaluations to track changes. The total study duration is six weeks per participant, and all results will be analyzed to compare the effectiveness of the two treatment approaches.

CONDITIONS

Brief Title

Effects of Epleys Maneuver Versus Semont-Plus Maneuver Combined with Brandt-Daroff Exercises on Dizziness and Quality of Life in Benign Paroxysmal Positional Vertigo

Who Can Participate

Age: 20Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Both genders
  • Positive Dix Hallpike test
  • Diagnosed with posterior canal benign paroxysmal positional vertigo (BPPV)
  • Recurrent episodes of dizziness
  • Age between 20 and 65 years
  • Positive Dix Hallpike test (listed twice in source)
Not Eligible

You will not qualify if you...

  • Negative Dix Hallpike test
  • Dizziness Handicap Inventory (DHI) score 54 or higher (severe dizziness)
  • History of trauma
  • Ankylosing spondylitis
  • Cervical pathology causing dizziness
  • Spinal cord injury
  • Carotid stenosis
  • Other vestibular disorders such as Meniere's disease, vestibular hypofunction, labyrinthitis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants receive either Epley's Maneuver or Semont-Plus Maneuver combined with Brandt-Daroff exercises for their dizziness related to posterior canal benign paroxysmal positional vertigo (BPPV).

Visits for treatment and assessments at baseline and at the end of 6 weeks

Trial Site Locations

Total: 1 location

1

Foundation University College of Physical Thrapy

Islamabad, Pakistan, 44000

Actively Recruiting

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Research Team

M

MARWA JAVED, DPT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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