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RecruitingNCT06738823Updated Dec 18, 2024

Effect of Wii Fit Training in Comparison to Vestibular Rehabilitation Training on Balance in Patients With Benign Paroxysmal Postional Vertigo

An interventional study of INTERVENTION GROUP : TRAINING WITH WIIFIT and VESTIBULAR REHABILITATION TRAINING in Benign Paroxysmal Positional Vertigo, Balance and Vertigo, sponsored by Foundation University Islamabad. Recruiting at 1 site in Pakistan. Open to participants aged 30 Years to 60 Years. Per ClinicalTrials.gov, last updated 2024-12-18.

Sponsored by Foundation University Islamabad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Jul 2024, registered Nov 2024).
  • Started Jul 2024; still recruiting 2 years 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
38
Allocation
Randomized
Ages
30 Years to 60 Years
Sex
All
01

Study summary

THIS STUDY IS A RANDOMIZED CONTROL TRIAL AND THE PURPOSE OF THE STUDY IS TO DETERMINE THE EFFECT OF WIIFIT TRAINING IN COMPARISON TO VESTIBULAR REHAB TRAINING ON BALANCE IN PATIENTS WITH BENIGN PAROXYSMAL POSITIONAL VERTIGO

Read the detailed description

Effects of wiifit training will be assessed for balance and vertigo which includes the parameters of balance training.

Benign Paroxysmal Positional Vertigo patients aged 30-60 years The participants will be assessed through Vestibular Rehabilitation questionnaire (VRBQ), Dizziness handicap inventory (DHI), Functional reach test, Clinical test for sensory integration in balance and vertigo symptom scale.

Informed consent will be taken after which the participants will be recruited into two groups, where one group will receive wiifit training and other group will receive vestibular rehabilitation training.

Base-line and post-treatment measurement will be taken for analysis.

02

Conditions studied

  • Benign Paroxysmal Positional Vertigo
  • Balance
  • Vertigo
03

In context

Benign Paroxysmal Positional Vertigo

75 studies on the registry are indexed under Benign Paroxysmal Positional Vertigo; 15 are open to participants now.

This study's planned enrollment of 38 is below the median of 78 across 62 interventional studies indexed under Benign Paroxysmal Positional Vertigo.

Browse Benign Paroxysmal Positional Vertigo studies →

Lead sponsor

Foundation University Islamabad is the lead sponsor of 255 studies on the registry; 142 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients diagnosed with benign paroxysmal positional vertigo.
  • Aged 30-60 years.
  • Ability to stand and walk independently.
  • Male and Female
  • Positive Dix Hallpike Test
  • DHI Scale: 36-42 (moderate Handicap)

Exclusion criteria

Exclusion Criteria:

  • patients with history of vestibular surgery or cochlear implantation.
  • Patients with history of seizures or epilepsy.
  • patients with a pacemaker or implantable cardioverter-defibrillator(ICD).
  • Patients with history of severe head injury or concussion within the past year.
  • No other vestibular disorders or conditions that may affect balance.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
38 participants (estimated)

Study arms

  • Experimental
    Experimental group A

    The participants will receive intervention through Wii fit training which includes games tight rope tension, ski slalom, penguin slide, table tilt, and heading for 6 total 6 weeks. 3 days per week session will be given for 30 minutes including 5-minutes warmup and cool down and 5 minutes of break in between to avoid fatigue.

    Procedure: INTERVENTION GROUP : TRAINING WITH WIIFIT

  • Active comparator
    Experimental group B

    The participants will receive vestibular rehabilitation training. The rehabilitation programme will include weight shifting, neck rotations, sit to stand exercises on padded mat, and head movements with eyes closed. The intervention will be given for 3 minutes, 3 days a week for total 6 weeks of time period.

    Procedure: VESTIBULAR REHABILITATION TRAINING

Interventions

  • ProcedureINTERVENTION GROUP : TRAINING WITH WIIFIT

    RCT (RANDOMIZED CONTROL TRIAL) GROUP 1 : Wii FIT TRAINING TIGHT ROPE TENSION, SKI SLALOM, PENGUIN SLIDE, TABLE TILT GROUP 2 : VESTIBULAR REHABILITATION TRAINING WEIGHT SHIFTING, NECK ROTATIONS, SIT TO STAND EXERCISES ON PADDED MAT AND HEAD MOVEMENTS WITH EYES CLOSED.

  • ProcedureVESTIBULAR REHABILITATION TRAINING

    WEIGHT SHIFTING, NECK ROTATIONS, SIT TO STAND EXERCISES ON PADDED MAT AND HEAD MOVEMENTS WITH EYES CLOSED.

06

What researchers measure

Primary outcomes

  1. Static Balance

    The Vestibular Rehabilitation Benefit Questionnaire (VRBQ) is a validated tool used to measure balance 0 means no problem, 100 means severe problem

    Time frame: 6 weeks

  2. Vertigo

    DHI scale is used to assess vertigo.The questionnaire consists of 25 items with 3 responses YES= 4 points SOMETIMES = 2 points and NO = 0 points. The total score ranges from 0 to 100, higher score indicating self perceived handicap due to dizziness.

    Time frame: 6 weeks

  3. Static Balance

    CTSIB of Biodex is used to assess static balance and has 4 components. a) Firm surface with eyes open; (Mean value 0.44)test the integration of visual,somatosensory and vestibular inputs. All sensory systems are available for balance. b) Firm surface with eyes closed; (mean value 0.80)evaluate the reliance on somatosensory input for balance and visual input is eliminated.c) Foam surface with eyes open; (Mean value; 0.79) Test the ability to use visual and vestibular inputs for balance when somatosensory inputs is unreliable,unstable surface. d) Foam surface with eyes closed; (mean value 2.41) primarily challenges the vestibular system by eliminating visual input and providing unreliable somatosensory feedback. The total mean of these 4 components is 1.11.

    Time frame: 6 weeks

  4. Dynamic balance

    Functional Reach test will be used to assess dynamic balance * Scoring: * Distance in centimeters or inches is recorded. * Normal values : * \<15 cm indicates a high fall risk in older adults

    Time frame: 6 weeks

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 18, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06738823
Responsible party
Sponsor
First posted
Dec 18, 2024
Start date
Jul 20, 2024
Primary completion
Dec 1, 2024
Completion
Dec 20, 2024 (estimated)
Last update
Dec 18, 2024

Study contacts

MAHAM AKBAR, DPT
Contact
mahamakbarch25@gmail.com
+92334-6406143

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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