Effects of Vestibular-Oriented Balance Training Versus Motor Dual Task Training on Balance, Postural Control, and Fall Risk in Chronic Stroke Survivors
1 other identifier
interventional
50
1 country
1
Brief Summary
This randomized controlled trial aims to compare the effectiveness of Vestibular-Oriented Balance Training and Motor Dual Task Training on balance, postural control, and fall risk among chronic stroke survivors. Forty-six participants diagnosed with chronic stroke will be randomly allocated into two intervention groups. Both groups will receive conventional physiotherapy along with their assigned intervention for six weeks. Outcome measures will include the Biodex Balance System (Overall Stability Index, Anterior-Posterior Stability Index, Medial-Lateral Stability Index and Fall Risk Index), Modified clinical test of sensory interaction on balance( m-CTISB). The findings will provide evidence regarding the most effective rehabilitation strategy for improving, Overall stability, and functional balance and reducing fall risk in chronic stroke survivors.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 10, 2026
CompletedFirst Submitted
Initial submission to the registry
August 5, 2026
CompletedFirst Posted
Study publicly available on registry
August 10, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 18, 2026
August 10, 2026
August 1, 2026
4 months
August 5, 2026
August 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Biodex Over all stability Index
Overall Stability Index (OSI) on the Biodex Balance System is a comprehensive score measuring how well a person controls their balance and keeps a moving platform level. Higher numbers mean more platform tilt and poorer balance control, while lower numbers show better stability and stronger neuromuscular coordination.
assessment at baseline and after 6 weeks
Biodex Fall Risk index
It measures a person's stability and risk of falling by tracking how much they sway on a moveable balance platform. Higher scores indicate poor stability and a higher likelihood of falls
at baseline and after 6 weeks
Modified clinical test of sensory interaction on balance
a clinical tool used to evaluate static postural control and identify which sensory systems (vision, vestibular, or somatosensory/proprioceptive) a patient relies on or struggles with to maintain balance.
at baseline and after 6 weeks
Secondary Outcomes (2)
Biodex APSI
at baseline and after 6 weeks
Biodex Medial/Lateral Stability Index
at baseline and after 6 weeks
Study Arms (2)
Vestibular-Oriented Balance Training
EXPERIMENTALParticipants will receive vestibular-oriented balance exercises together with conventional physiotherapy for five weeks
Motor Dual Task Training
ACTIVE COMPARATORParticipants will receive motor dual-task balance training together with conventional physiotherapy for five weeks
Interventions
Participants will receive vestibular-oriented balance exercises together with conventional physiotherapy for five weeks
Participants will receive motor dual-task balance training together with conventional physiotherapy for five weeks.
Eligibility Criteria
You may qualify if:
- Diagnosis of ischemic stroke.
- Stroke duration ≥6 months.
- Rhomberg scale
- MMSE ≥ 24
- Able to walk with or without assistive device.
- Able to understand commands
- Willing to participate and provide consent aged between 40-70 years.
You may not qualify if:
- Severe visual impairements which effect balance.
- Participants with acute or sub acute stroke \<6 moths.
- Uncontrolled hypertension
- Uncontrolled diabetes
- Other neurological disorders such as Parkinson's disease or multiple sclerosis and Alzheimer's
- Participation in any other interventional trail.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Armed Forces Institute of Rehabilitation Medicine Rawalpindi, Pakistan
Rawalpindi, 46000, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
August 5, 2026
First Posted
August 10, 2026
Study Start
July 10, 2026
Primary Completion (Estimated)
November 15, 2026
Study Completion (Estimated)
December 18, 2026
Last Updated
August 10, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share