Ai Chi-Based Rehabilitation for Peripheral Unilateral Vestibular Dysfunction

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-70
SponsorGaziosmanpasa Research and Education Hospital

About this trial

This study aims to evaluate the effects of an Ai Chi-based rehabilitation program on balance, dizziness severity, and quality of life in patients with unilateral peripheral vestibular hypofunction. Participants will be randomly assigned to either a control group receiving standard home-based vestibular rehabilitation exercises or an intervention group receiving additional Ai Chi sessions. The intervention will be conducted over a 4-week period with a total of 10 sessions under the supervision of a certified therapist.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age between 18 and 70 years

Diagnosis of unilateral peripheral vestibular hypofunction

Presence of dizziness symptoms for at least 3 months

Ability to participate in Ai Chi and aquatic exercise program

Disqualifiers

Inability to complete assessment tests and questionnaires

Severe systemic disease that may interfere with exercise participation

Central vestibular disorders

Berg Balance Scale score ≤20

Trial design

Design model

Parallel

Treatments tested in this trial

  • Ai Chi-based exercise program

    Behavioral

    Ai Chi-based exercise program is a structured aquatic therapy approach consisting of slow, continuous, and controlled movements combined with breathing techniques. The program will be conducted in a pool environment over 4 weeks, with a total of 10 sessions delivered as group sessions under the supervision of a certified therapist. The exercises are designed to enhance balance, postural control, proprioceptive input, and multisensory integration, thereby supporting central compensation in patients with vestibular dysfunction.

  • Home-Based Vestibular Rehabilitation

    Behavioral

    Participants will receive a structured home-based vestibular rehabilitation program including gaze stabilization, head movement, balance, and postural control exercises. The program aims to promote vestibulo-ocular reflex adaptation, improve postural stability, and reduce dizziness-related symptoms. Participants will be instructed to perform the exercises regularly, and adherence will be monitored using exercise logs.

Treatment groups

38 Participants
are divided into 2 treatment groups
Group A: Ai Chi GroupExperimental treatment 2 interventions
Group B: Control GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in balance performance assessed by Berg Balance Scale

Change in balance performance will be assessed using the Berg Balance Scale (BBS). The BBS consists of 14 items scored from 0 to 4, with a total score ranging from 0 to 56. Higher scores indicate better balance performance. balance performance will be assessed using the Berg Balance Scale in participants receiving Ai Chi-based exercise program in addition to home-based vestibular rehabilitation, compared with participants receiving home-based vestibular rehabilitation alone.

Time frame
Baseline, immediately after the 4-week intervention, and 2 months after the end of treatment

Secondary outcomes

1

Change in dizziness-related disability will be assessed using the Dizziness Handicap Inventory (DHI). The DHI consists of 25 items with a total score ranging from 0 to 100. Higher scoredizziness-related disability assessed by Dizziness Handicap Inventory

Change in dizziness-related disability will be assessed using the Dizziness Handicap Inventory.

Time frame
Baseline, immediately after the 4-week intervention, and 2 months after the end of treatment
2

Change in dizziness severity assessed by Vertigo Symptom Scale-Short Form

Change in vestibular symptoms will be assessed using the Vestibular Symptoms Scale (VSS). The VSS consists of 15 items evaluating the frequency of vestibular symptoms. Each item is scored from 0 to 4, with a total score ranging from 0 to 60. Higher scores indicate more severe symptoms. dizziness severity will be assessed using the Vertigo Symptom Scale-Short Form.

Time frame
Baseline, immediately after the 4-week intervention, and 2 months after the end of treatment
3

Change in kinesiophobia assessed by Tampa Kinesiophobia Scale

Change in kinesiophobia will be assessed using the Tampa Scale for Kinesiophobia (TSK). The TSK consists of 17 items scored from 1 to 4, with total scores ranging from 17 to 68. Higher scores indicate greater fear of movement.

Time frame
Baseline, immediately after the 4-week intervention, and 2 months after the end of treatment
4

Change in quality of life assessed by Short Form-36

Change in quality of life will be assessed using the Short Form-36 Health Survey (SF-36). The SF-36 consists of 8 subscales scored from 0 to 100, with higher scores indicating better health status.

Time frame
Baseline, immediately after the 4-week intervention, and 2 months after the end of treatment

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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