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Korean Medicine Clinical Pathway for Persistent Postural-Perceptual Dizziness

A Pilot Application Study of a Prototype Korean Medicine Clinical Pathway for Persistent Postural-Perceptual Dizziness (PPPD) in a Korean Medicine Hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010114
Enrollment
30
Registered
2025-01-10
Start date
2025-03-03
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

None listed

Interventions

Others(korean medicine clinical pathway for persistent Postural-perceptual dizziness) : Subjects can choose between korean medicine clinical pathway (CP)-applied treatment and conventional korean medi

Sponsors

Dong-Eui University Oriental Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult male or female aged 19 or older and under 65 years old 2. Patients who are diagnosed with Persistent Postural-Perceptual Dizziness below and complain of dizziness with a DHI score of 16 or higher or an NRS score of 4 or higher - Persistent non-rotational dizziness for more than 3 months - Hypersensitivity to one's own movement or movement of the surrounding environment for more than 3 months - Symptoms worsen in a complex visual environment or when precise visual tasks such as reading or using a computer are required 3. Those who have agreed by signing the written consent form provided

Exclusion criteria

Exclusion criteria: 1. Those diagnosed with dizziness due to cardiovascular disease (arrhythmia, heart valve disease, anemia, orthostatic hypotension, coronary artery disease, etc.) 2. Those diagnosed with dizziness due to active or uncontrolled diseases (e.g., uncontrolled diabetes, hypertension, other respiratory and endocrine diseases) 3. Those diagnosed with dizziness due to medication currently being taken 4. Those diagnosed with serious chronic or terminal diseases (malignant tumor, chronic renal failure, tuberculosis, etc.) 5. Patients complaining of dizziness associated with cervical movement or cervical posture accompanied by neck pain or stiffness 6. Those diagnosed with abnormalities through neurological examinations and brain imaging tests 7. Those who have received other treatment (non-steroidal anti-inflammatory drugs, steroids, etc.) due to dizziness caused by vestibular dysfunction within the past month 8. Those who are pregnant, plan to become pregnant during the trial period, or are breastfeeding 9. Those suspected of alcohol or drug abuse 10. Those who have participated in another clinical trial within 1 month of the start date of the intervention 11. Those with communication disorders that make it difficult to follow the investigator's instructions 12. Those who are judged unsuitable for trial participation by the principal investigator or investigators

Design outcomes

Primary

MeasureTime frame
Change in Dizziness Handicap Inventory (DHI): Difference in score after 4 weeks (V9) compared to baseline (V2)

Secondary

MeasureTime frame
Change in the Numeric Rating Scale (NRS): Difference in scores each week (V3-9) compared to baseline (V2);Change in quality of life assessment tool(EQ-5D-5L): V9 score difference compared to V2;Patient Satisfaction Survey;Adverse Events

Countries

Korea, Republic of

Contacts

Public Contactsoohyung jeon

Dong-Eui University Oriental Medicine Hospital

jsoohyung@hanmail.net+82-51-850-8904

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026