- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07267988
Additional Effects Of Brandt-Daroff Exercises With GANS Maneuver On Dizziness And Quality Of Life In Patients With BPPV
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Rabia Ejaz, DPT
- Phone Number: +92 3145281989
- Email: rabiaejaz57@gmail.com
Study Locations
-
-
-
Islamabad, Pakistan, 44000
- Recruiting
- Foundation University College of Physical Therapy
-
Contact:
- Furqan Ahmed Siddiqi, Phd
- Phone Number: 602 051 5788582
- Email: principal.fucp@fui.edu.pk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Diagnosed Patients of Benign Paroxysmal Vertigo (BPPV)
- Age between 18-60
- Acute and Chronic BPPV Patients
- Positive Dix-Hallpike Test
- DHI Scale: Mild-Severe (0-100)
Exclusion Criteria:
- Patients with a history of vestibular surgery or cochlear
- Patients with a history of seizures or epilepsy
- Patients with a pacemaker or implantable cardioverter-defibrillator (ICD)
- Patients with a history of severe head injury or concussion within the past year
- No other vestibular disorders or conditions that may affect balance (e.g., Meniere's disease, labyrinthitis
- No musculoskeletal or neurological conditions that may affect balance (e.g., stroke, Parkinson's disease)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: GANS Maneuver with Brand-Daroff Exercises
GANS Maneuver include:
|
The intervention program spans six weeks and involves both supervised Gans Maneuver sessions and home-based Brandt-Daroff exercises. Participants will attend two supervised Gans sessions per week, with each session consisting of three repetitions of the maneuver. In addition, participants will perform Brandt-Daroff exercises at home twice daily, with each cycle consisting of three repetitions. This combination of supervised and home-based practice will be maintained consistently throughout all six weeks. Across the entire program, participants will complete a total of 12 supervised Gans sessions and 36 Brandt-Daroff home sessions. |
|
Active Comparator: GANS Maneuver
GANS Maneuver include:
|
The control group will participate in a structured six-week intervention program consisting exclusively of the Gans Maneuver.
Participants will attend two supervised sessions per week, ensuring consistent oversight and proper technique throughout the program.
Each session will include three repetitions of the maneuver, with participants allowed a rest period of 30 to 60 seconds between repetitions to prevent fatigue and maintain the quality of each movement.
This frequency and volume are maintained consistently across all six weeks to provide a standardized exposure, allowing for accurate comparison with other intervention groups.
Over the entire six-week period, participants will complete a total of 12 supervised sessions, each with three repetitions, summing up to 36 repetitions across the intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dizziness
Time Frame: 6 weeks
|
Dizziness Handicap Inventory Scale(DHI): 25 Items (scoring16-54) where 16-34 = Mild handicap , 36-52 = moderate handicap , 52+ = severe handicap
|
6 weeks
|
|
Quality Of Life In BPPV patients
Time Frame: 6 weeks
|
Vestibular Activities and Participation Scale (VAP): A 34-item, (1-4 score) , 1 = mild limitations, 2 = moderate limitation, and 3 = severe limitations, 4=extreme limitation
|
6 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FUI/CTR/2025/12
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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