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Exercise and Vestibular Hypofunction (EXERVEST)

Primary Purpose

Vestibular Disease, Vestibular Disorder, Vestibular Vertigo

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Exercise for bilateral or unilateral vestibular hypofunction patients
Conventional rehabilitation treatment
Sponsored by
University of the Basque Country (UPV/EHU)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vestibular Disease focused on measuring Vestibular hypofunction, Exercise, Balance training, Imbalance

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient with unilateral vestibular hypofunction.
  • More than 6 months since the onset of vestibular hypofunction (chronic instability).
  • Age between 18-65 years old.
  • No previous rehabilitation treatment for vestibular hypofunction other than home exercises.

Exclusion Criteria:

  • Fluctuating instability (not present every day).
  • Recent onset instability (less than 6 months old, susceptible to complete clinical recovery).
  • Current neurological pathology.
  • History of neurosurgical disease, cerebrovascular disease, neurodegenerative disease or with central nervous system sequelae.
  • Uncorrected ocular disorders.
  • History of peripheral neuropathy in the lower extremities.
  • Arthropathy or motor defects in lower limbs.
  • Prolonged use of sedatives or vestibular suppressant medication.
  • Significant medical disorders: including uncontrolled arterial hypertension, chronic or recurrent respiratory, neuromuscular or psychiatric diseases; musculoskeletal problems that interfere with physical exercise; immunodeficient diseases or a positive HIV test; anemia, blood disorders, chronic thrombotic disorders or hypercoagulant states; malignant tumors within the last five years, with the exception of therapeutically controlled skin cancer; any other disease that may be affected or aggravated by physical exercise.
  • Being pregnant or breastfeeding.
  • Have plans to be out of town for more than two weeks.

Sites / Locations

  • Faculty of Education and SportRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

EX Group

AC Group - ATTENTION CONTROL GROUP

Arm Description

Conventional rehabilitation treatment plus exercise intervention under the supervision of exercise specialists two non-consecutive days per week for eight weeks.

Conventional rehabilitation treatment at home with unsupervised exercise intervention

Outcomes

Primary Outcome Measures

Balance
Computerized Dynamic Posturography testing can objectively measure a patient's three sensory inputs at one time during the Sensory Oorganization Test. It can provide insight into where the balance disturbance may be developing from and more importantly, which one of the sensory inputs shows a problem. The human body uses three sensory inputs to maintain balance proper balance, they are: Vestibular (inner ear system), Somatosenory (feet, ankles, joints), Vision (eyes). These sensory inputs interact with the brain, which then drive and control our motor functions. Computerized Dynamic Posturography is a unique assessment technique used to objectively quantify and differentiate among these three sensory inputs, along with motor, and central adaptive impairments to balance control.

Secondary Outcome Measures

Health-related Quality of life
Measured by Dizziness Handicap Inventory Questionnaire It contains a total score (100 items) and scores in the physical (28 items), functional (36 items) and emotional (36 items) subscales. Scores greater than 10 points should be referred to balance specialists for further evaluation. 16-34 Points (mild handicap) 36-52 Points (moderate handicap) 54+ Points (severe handicap)
Depression
Measured by Beck Depression Inventory (BDI) 21 Likert-type items. The maximum score is 63 points, with the following classification: 0-13, minimal depression; 14-19, mild depression; 20-28, moderate depression; and 29-63, severe depression.
Physical activity level
Measured by accelerometry (8 days) in the non-dominant wrist.
Blood pressure
Ambulatory blood pressure monitoring (AMBP) is accomplished with a special device that consists of a blood pressure cuff that is worn on the arm and is attached to a small recording device that you wear on your belt. The participant will wear the ABPM device for 24 hours, and it records your blood pressure periodically (30-min intervals) throughout that period, during your routine daily activities and while you are sleeping.
Body composition
Biolectrical impedance for estimating % of body fat-mass, muscle-mass, and water.
Cardiorespiratory fitness
Peak Cardiopulmonary exercise test on bicycle ergometer.
Anxiety
Beck Anxiety Inventory (BAI). 21 items. The maximum score is 63 points, 25.7±11.4 being considered an anxiety score.
Physical activity and sedentary behaviour
International physical activity questionnaire (IPAQ) short-version. It consists of seven questions to capture average daily time spent sitting, walking, and engaging in moderate and vigorous PA over the last seven days.
Assessment of gait, balance and risk of falls
Dynamic Gait Index (DGI): composed of 8 exercises each scored from 0 (severe impairment) to 3 (highest level of functionality); maximum score: 24 points; a score < 19 is predictive of falls.
Waist circumference
Stand and place a tape measure around your middle, just above your hipbones. Measured in cm
Body mass index (BMI)
BMI is a person's weight in kilograms divided by the square of height in meters.

Full Information

First Posted
November 25, 2021
Last Updated
April 12, 2023
Sponsor
University of the Basque Country (UPV/EHU)
Collaborators
Bioaraba
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1. Study Identification

Unique Protocol Identification Number
NCT05192564
Brief Title
Exercise and Vestibular Hypofunction
Acronym
EXERVEST
Official Title
Supervised Exercise as an Adjuvant Program in People With Chronic Bilateral or Unilateral Vestibular Hypofunction: EXERVEST Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 8, 2022 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
July 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of the Basque Country (UPV/EHU)
Collaborators
Bioaraba

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Vestibular hypofunction is a heterogeneous clinical entity that arises after a vestibular pathway injury, which if not properly compensated becomes chronic, and very often disabling, presenting with postural instability, blurred vision with cephalic movement, oscillopsia, and subjective sensation of dizziness and imbalance. People diagnosed with vestibular hypofunction, because of their clinical condition, often tend to reduce physical activity and lead to a sedentary life, despite the fact that exercise has been shown to improve postural stability, and it is a determining factor in recovery after vestibular injury. Physical activity improves the quality of life and reduces the risk of falls. Supervised exercise is, therefore, among the potentially beneficial adjuvant programs in this population, although little has been studied in comparison with other pathologies. Furthermore, in vestibular hypofunction, there is insufficient evidence on specific interventions in specific clinical situations, the amount of exercise, and the optimal duration of the programs. Therefore, the aims of the study are 1) to analyze the effects on balance by an 8-week period of a supervised exercise program in people with a diagnosis of bilateral or unilateral vestibular hypofunction and 2) to examine the effect of six-months detraining subsequent to intervention. Secondary objectives are to examine the additional effect of the intervention on health-related quality of life, psychological well-being, cardiorespiratory fitness, body composition, blood pressure, physical activity level, sedentary behavior, and sleep quality.
Detailed Description
Interventional study with two randomized groups (attention control '[AC] and exercise group,[EX]) with assessment pre and post-intervention (8 weeks) and 6 months follow-up. The AC group will perform only the home vestibular rehabilitation exercises that are usually prescribed in consultation with this type of patient, performing the same assessments as the intervention group in all phases of the study. The participants in the EX group will exercise under the supervision of specialists in exercise and sports physical educators two non-consecutive days per week for eight weeks at the Faculty of Education and Sport of the University of the Basque Country (UPV/EHU). All sessions will start and end with blood pressure measurements and exercise intensity will be monitored by heart rate monitors (Polar Electro, Kempele, Finland) and through the original Borg scale (6-20). All sessions will include a 5-10 min warm-up with joint mobility exercises and gait technique and a 10 min cooldown with basic stretching exercises and controlled breathing. The main part of the session will consist of: 1) balance exercises, multidirectional displacements and strength with postural control, implementing 8-10 exercises integrating the main muscle groups and motor patterns, 2) aerobic exercise on bicycle (15 min) developed progressively in intensity (R1-mild, R2-moderate, R3-vigorous) implementing an intervallic design at low volume. The physical exercise intensity ranges (R1-mild, R2-moderate, R3-vigorous) will be defined on an individualized basis from the initial stress test and based on ventilatory thresholds. At the end of the intervention, participants will be provided with information on physical activity recommendations. Both intervention and control group patients will have all antivertiginous drugs withdrawn.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vestibular Disease, Vestibular Disorder, Vestibular Vertigo
Keywords
Vestibular hypofunction, Exercise, Balance training, Imbalance

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
DESIGN: Controlled, randomized, prospective, single-blind (staff of the otorhinolaryngology department) intervention study carried out in a cohort of patients (over 18 yr old) with a diagnosis of bilateral or unilateral vestibular hypofunction divided into two groups: intervention group with exercise + conventional rehabilitation treatment (EX group) and a group without intervention that will receive only conventional rehabilitation treatment (attention control group, AC).
Masking
Investigator
Allocation
Randomized
Enrollment
78 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
EX Group
Arm Type
Experimental
Arm Description
Conventional rehabilitation treatment plus exercise intervention under the supervision of exercise specialists two non-consecutive days per week for eight weeks.
Arm Title
AC Group - ATTENTION CONTROL GROUP
Arm Type
Active Comparator
Arm Description
Conventional rehabilitation treatment at home with unsupervised exercise intervention
Intervention Type
Other
Intervention Name(s)
Exercise for bilateral or unilateral vestibular hypofunction patients
Intervention Description
Physical Activity intervention with balance exercises, multidirectional displacements, and strength with postural control, implementing 8-10 exercises integrating the main muscle groups and motor patterns, aerobic exercise on bicycle (15 min) developed progressively in intensity (R1-mild, R2-moderate, R3-vigorous) implementing an intervallic design in low volume.
Intervention Type
Other
Intervention Name(s)
Conventional rehabilitation treatment
Intervention Description
Vestibular rehabilitation exercises counseling
Primary Outcome Measure Information:
Title
Balance
Description
Computerized Dynamic Posturography testing can objectively measure a patient's three sensory inputs at one time during the Sensory Oorganization Test. It can provide insight into where the balance disturbance may be developing from and more importantly, which one of the sensory inputs shows a problem. The human body uses three sensory inputs to maintain balance proper balance, they are: Vestibular (inner ear system), Somatosenory (feet, ankles, joints), Vision (eyes). These sensory inputs interact with the brain, which then drive and control our motor functions. Computerized Dynamic Posturography is a unique assessment technique used to objectively quantify and differentiate among these three sensory inputs, along with motor, and central adaptive impairments to balance control.
Time Frame
8-week time
Secondary Outcome Measure Information:
Title
Health-related Quality of life
Description
Measured by Dizziness Handicap Inventory Questionnaire It contains a total score (100 items) and scores in the physical (28 items), functional (36 items) and emotional (36 items) subscales. Scores greater than 10 points should be referred to balance specialists for further evaluation. 16-34 Points (mild handicap) 36-52 Points (moderate handicap) 54+ Points (severe handicap)
Time Frame
8-week time
Title
Depression
Description
Measured by Beck Depression Inventory (BDI) 21 Likert-type items. The maximum score is 63 points, with the following classification: 0-13, minimal depression; 14-19, mild depression; 20-28, moderate depression; and 29-63, severe depression.
Time Frame
8-week time
Title
Physical activity level
Description
Measured by accelerometry (8 days) in the non-dominant wrist.
Time Frame
8-week time
Title
Blood pressure
Description
Ambulatory blood pressure monitoring (AMBP) is accomplished with a special device that consists of a blood pressure cuff that is worn on the arm and is attached to a small recording device that you wear on your belt. The participant will wear the ABPM device for 24 hours, and it records your blood pressure periodically (30-min intervals) throughout that period, during your routine daily activities and while you are sleeping.
Time Frame
8-week time
Title
Body composition
Description
Biolectrical impedance for estimating % of body fat-mass, muscle-mass, and water.
Time Frame
8-week time
Title
Cardiorespiratory fitness
Description
Peak Cardiopulmonary exercise test on bicycle ergometer.
Time Frame
8-week time
Title
Anxiety
Description
Beck Anxiety Inventory (BAI). 21 items. The maximum score is 63 points, 25.7±11.4 being considered an anxiety score.
Time Frame
8-week time
Title
Physical activity and sedentary behaviour
Description
International physical activity questionnaire (IPAQ) short-version. It consists of seven questions to capture average daily time spent sitting, walking, and engaging in moderate and vigorous PA over the last seven days.
Time Frame
8-week time
Title
Assessment of gait, balance and risk of falls
Description
Dynamic Gait Index (DGI): composed of 8 exercises each scored from 0 (severe impairment) to 3 (highest level of functionality); maximum score: 24 points; a score < 19 is predictive of falls.
Time Frame
8-week time
Title
Waist circumference
Description
Stand and place a tape measure around your middle, just above your hipbones. Measured in cm
Time Frame
8-week time
Title
Body mass index (BMI)
Description
BMI is a person's weight in kilograms divided by the square of height in meters.
Time Frame
8-week time

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient with bilateral or unilateral vestibular hypofunction. More than 6 months since the onset of vestibular hypofunction (chronic instability). Age over 18 years old. No previous rehabilitation treatment for vestibular hypofunction other than home exercises. Exclusion Criteria: Fluctuating instability (not present every day). Recent onset instability (less than 6 months old, susceptible to complete clinical recovery). Current neurological pathology. History of neurosurgical disease, cerebrovascular disease, neurodegenerative disease or with central nervous system sequelae. Uncorrected ocular disorders. History of peripheral neuropathy in the lower extremities. Arthropathy or motor defects in lower limbs. Prolonged use of sedatives or vestibular suppressant medication. Significant medical disorders: including uncontrolled arterial hypertension, chronic or recurrent respiratory, neuromuscular or psychiatric diseases; musculoskeletal problems that interfere with physical exercise; immunodeficient diseases or a positive HIV test; anemia, blood disorders, chronic thrombotic disorders or hypercoagulant states; malignant tumors within the last five years, with the exception of therapeutically controlled skin cancer; any other disease that may be affected or aggravated by physical exercise. Being pregnant or breastfeeding. Have plans to be out of town for more than two weeks.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
SARA MALDONADO-MARTIN, PhD
Phone
+34945013534
Email
sara.maldonado@ehu.eus
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
SARA MALDONADO-MARTIN, PhD
Organizational Affiliation
University of the Basque Country (UPV/EHU)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty of Education and Sport
City
Vitoria-gasteiz
State/Province
Basque Country
ZIP/Postal Code
01007
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
SARA MALDONADO-MARTIN, PhD
First Name & Middle Initial & Last Name & Degree
ASIER LEKUE, MD

12. IPD Sharing Statement

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Exercise and Vestibular Hypofunction

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