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Benign Paroxysmal Positional Vertigo in Older Adults

Not Applicable
Conditions
Benign Paroxysmal Positional Vertigo
Interventions
Other: Particle Repositioning Maneuver
Registration Number
NCT05013684
Lead Sponsor
Hasselt University
Brief Summary

Despite the growing research on Benign Paroxysmal Positioning Vertigo (BPPV), the impact and treatment efficacy on balance, physical activity (and consequently) frailty in elderly is lacking. Also, the added value of the video Head Impulse Test (vHIT) in this population has never been studied before. With insights gained from this research, we hope to contribute to an efficient treatment of BPPV in this growing population and to minimize its impact and healthcare burden.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
90
Inclusion Criteria
  • Persons ≥ 65 years old
  • Able to stand independent for at least 30 seconds
  • Able to walk (with or without) walking aid for at least 10 meters
  • Patients diagnosed with posterior semicircular canal BPPV
  • Patients diagnosed with lateral-semicircular canal BPPV
Exclusion Criteria
  • Unable to understand and follow simple instructions (e.g. due to severe dementia, hearing loss or visual impairment)
  • Persons temporarily or permanently living in a residential or psychiatric care centre, a home for the disabled or rehabilitation centre
  • Persons with contra-indications for the diagnostic maneuver, vHIT or caloric irrigation test (e.g. severe limitation in mobility of the cervical spine of perforation of the tympanic membrane)
  • Persons with other (acute) vestibular disorders and who as a result no longer meet the above mentioned diagnostic criteria for BPPV
  • Persons with evolutionary disorders of the central nervous system (e.g. multiple sclerosis, Parkinson's disease, amyotrophic lateral sclerosis).
  • Persons who are already taking antivertigo drugs.
  • Persons still in the rehabilitation phase after an orthopedic or cardiovascular incident.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Older adults with BPPVParticle Repositioning Maneuver-
Primary Outcome Measures
NameTimeMethod
The mini Balance Evalutation System test (miniBEStest)month 6

The MiniBEStest is a 14-item test that measures 4 different balance control systems: anticipatory postural adjustments, reactive postural control, sensory orientation and dynamic gait. Items are scored on a 3-level ordinal scale.

The CTSIB is used to assess sensory contributions to postural control during 6 sensory conditions: stand on firm surface with eyes open, stand on foam surface with eyes open, stand on firm surface with visual conflict dome, stand on foam surface with visual conflict dome, stand on firm surface with eyes closed and stand on foam surface with eyes closed.

10 meter walk testmonth 6

During the 10 meter walk test the participant is instructed to walk 10 meter at his/her preferred walking speed. Gait parameters will be assessed.

physical activity level measurde by an accelerometer (MOX)month 6

Objective measurement of physical activity level of four days will be done by an accelerometer (MOX), that measures time spent in certain positions. The accelerometer is attached to the upper leg of the participant.

The International Physical Activity QuestionnaireMonth 6

used to measure the level of physical activity by questionnaire. This questionnaire consists of 31 questions divided over 5 subcategories. A higher score means a higher level of physical activity.

Frailtymonth 6

Frailty is defined as a clinical syndrome in which three or more of the following criteria are present: unintentional weight loss (more than 3 kg during last year and/or BMI ≤ 21 kg/m2), weakness (unable to rise from a chair), self-reported exhaustion, slow walking speed (velocity on 10 meter walk test) and low physical activity (answering 'no' to the question 'do you perform regular physical activity as walking, gardening or sport).

Secondary Outcome Measures
NameTimeMethod
Walking aidThroug study completion, an average of 6 months

Walking aid wil be questioned

the 15-item Geriatric Depression ScaleMonth 6

Depressive feeling will be measured with the 15-item Geriatric Depression Scale

medication useThroug study completion, an average of 6 months

medication use will be questioned

the Montreal Cognitive Assessment (MOCA)Baseline

Cognitive function of older adults with BPPV will be compared to cognitive function of older adults without BPPV. Cognitive function will be assessed with the Montreal Cognitive Assessment (MOCA). MOCA assesses short term memory, visuospatial abilities, executive functions, attention and working memory, language and orientation to time and place.

Living situationThroug study completion, an average of 6 months

Living situation wil be questioned

BPPV-symptomatologyThroug study completion, an average of 6 months
AgeThroug study completion, an average of 6 months

Years

HeightThroug study completion, an average of 6 months

meters

Fall historyUp to the end of the study

Fall History will be measured during the follow-up period by a 2-weekly telephone interview.

Trial Locations

Locations (1)

Ziekenhuis Oost-Limburg

🇧🇪

Genk, Belgium

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