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Comparison of Home-Based Exercise on the Posterior Canal Benign Paroxysmal Positional Vertigo Symptoms

U

University of Malaya

Status

Completed

Conditions

Benign Paroxysmal Positional Vertigo

Treatments

Other: Brandt-Daroff Exercise
Other: Self Epley Manoeuvre

Study type

Interventional

Funder types

Other

Identifiers

NCT03230513
MREC ID NO: 20155-1337

Details and patient eligibility

About

Benign paroxysmal positional vertigo (BPPV) is the most common vestibular disorder in adults and the treatment of choice is by particle repositioning manoeuvres (PRM). This study aims to compare the treatment efficacy of two home-based exercises, self-Epley manoeuvre (SEM) and Brandt-Daroff exercise (BDE) in patients with posterior canal BPPV based on vertigo resolution, reduction of vertigo intensity, the Dizziness Handicap Inventory scores and the conversion of a positive to negative Dix-Hallpike test.

Full description

Study Objective:

To compare the efficacy of the self-Epley manoeuvre to the Brandt-Daroff exercise in resolving vertigo symptoms in patients with unilateral posterior canal BPPV.

Study Design:

Single-blind randomized controlled study

Sample Size:

Fifty patients were recruited in the study and were divided with 25 patients in each treatment arm.

Study Method:

Patients who satisfy the inclusion criteria and have given informed consent were randomized into the 2 treatment groups. A dedicated physiotherapist will demonstrate the selected exercise (either SEM or BDE) and observed the patient performing the exercise twice to ensure the ability of the patient to perform it correctly at home. A diary was provided for the patients to chart the therapy sessions performed at home as well as a pamphlet with simple illustrated instructions of the chosen exercise. The patients were asked to perform the home-based exercise for 2 weeks.

Primary Outcome Measure

  • Resolution of vertigo symptoms in patients with unilateral posterior canal BPPV.

Secondary Outcome Measures

  • Vertigo resolution at 1 and 6 months;
  • The conversion of positive to negative Dix-Hallpike test between both groups after 1 month;
  • Vertigo intensity in unresolved vertigo patients at 1 & 6 months;
  • The Dizziness Handicap Inventory between both groups at 1 and 6 months.

Enrollment

50 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients who have had symptoms of vertigo for at least 1 week duration,
  • patients with a documented positive Dix-Hallpike test on referral,
  • patients with intact cognitive function and had the ability to communicate and understand instructions to perform a home-based exercise.

Exclusion criteria

  • patients with history of prior ear surgery,
  • patients with orthopaedic or connective tissue disorder that impairs functional neck or trunk range of motion,
  • patients with a significant neurological disorder or spinal cord damage, and
  • patients who have been prescribed with home-based exercises for BPPV.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

Self Epley Manoeuvre
Active Comparator group
Description:
Self Epley Manoeuvre.
Treatment:
Other: Self Epley Manoeuvre
Brandt-Daroff Exercise
Active Comparator group
Description:
Brandt-Daroff Exercise.
Treatment:
Other: Brandt-Daroff Exercise

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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