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Effects of vestibular rehabilitation for patients with persistent postural-perceptual dizziness: A randomized controlled study

Effects of vestibular rehabilitation for patients with persistent postural-perceptual dizziness: A randomized controlled study - Effects of vestibular rehabilitation for patients with PPPD

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055880
Enrollment
30
Registered
2024-10-18
Start date
2024-10-18
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Persistent Postural-Perceptual Dizziness

Interventions

Vestibular rehabilitation Intervention period: 6 weeks Usual treatment Intervention period: 6 weeks

Sponsors

Mejiro University Ear Institute Clinic, Otolaryngology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with persistent postural-perceptual dizziness 2. Total score of 31 or more on the Dizziness Handicap Inventory (DHI)

Exclusion criteria

Exclusion criteria: 1. Patients who have previously undergone vestibular rehabilitation 2. Cognitive impairment 3. Central neurological symptoms 4. Patients taking SSRI or SNRI in the last month

Design outcomes

Primary

MeasureTime frame
Dizziness Handicap Inventory (DHI)

Secondary

MeasureTime frame
Visual vertigo analogue scale (VVAS) Functional gait assessment (FGA) Dynamic gait index (DGI) Balance Error Scoring System (BESS) Dynamic Visual Acuity (DVA) Stabilometry Activities-specific balance confidence (ABC) scale Niigata PPPD questionnaire (NPQ) Hospital anxiety and depression scale (HADS) Dizziness catastrophizing Scale (DCS) Central Sensitization Inventory (CSI) Vestibular Activities Avoidance Instrument (VAAI) Pittsburgh sleep quality index (PSQI)

Countries

Japan

Contacts

Public ContactRyozo Tanaka

Mejiro University Department of Physical Therapy, Faculty of Health Sciences

r.tanaka@mejiro.ac.jp048-797-2131

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026