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NCT Number: NCT06738823

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

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

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Key information

Age range

30 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Foundation University College of Physical Therapy

Islamabad, 44000, Pakistan

Location status: Recruiting

Location contact

SANA KHALID, MS-NMPT

CONTACT

[email protected]

+92344-4218174

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

  • 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.

Treatment and study plan

INTERVENTION GROUP : TRAINING WITH WIIFIT

Procedure

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.

VESTIBULAR REHABILITATION TRAINING

Procedure

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

Primary outcomes

  1. Static Balance

    Time frame: 6 weeks

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

  2. Vertigo

    Time frame: 6 weeks

    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.

  3. Static Balance

    Time frame: 6 weeks

    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.

  4. Dynamic balance

    Time frame: 6 weeks

    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

Study contacts

Contact information is provided by the study sponsor or research team.

MAHAM AKBAR, DPT

CONTACT

[email protected]

+92334-6406143

Sponsors and collaborators

Lead sponsor

Foundation University Islamabad

Other

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Dec 18, 2024
Registry last updated
Dec 18, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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