Acupuncture Trial Protocol for Post-Stroke Vascular Vertigo
by Lina Pang·Updated 3mo ago
142.5 KB1files
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Description
234 patients with post-stroke vascular vertigo are enrolled in a multicenter, randomized controlled trial. The study protocol details a 3-week intervention comparing acupuncture, sham acupuncture, and active drug groups, with follow-ups at 8 and 20 weeks. Primary and secondary outcomes include the Dizziness Handicap Inventory, anxiety scales, health surveys, and multimodal MRI data.
Use Cases
Analyze the relationship between Dizziness Handicap Inventory (DHI) scores and treatment group assignment (acupuncture, sham, drug) across 234 patients.
Investigate correlations between Expectation Rating Scale (ERS) results and clinical efficacy outcomes like the SF-36 health survey.
Compare safety profiles by examining adverse event records across the three intervention arms over the 20-week follow-up period.
Explore central nervous system mechanisms by analyzing multimodal magnetic resonance imaging (MRI) data in relation to Dizziness and Anxiety Rating Scale (DARS) scores.
Strengths
Protocol for a rigorously designed multicenter, double-blind, randomized controlled trial with 234 enrolled patients.
Includes multiple clinical and mechanistic outcome measures: DHI, DARS, SF-36, TCD, and multimodal MRI.
Study has received ethics approval (approval no. 2025KL-062) and is registered (ITMCTR2025001283).
Limitations
Data is a 142.5 KB study protocol PDF, not the raw clinical trial results or a structured dataset.
The sample size of 234 patients, while planned, may limit statistical power for subgroup analyses.
Geographic coverage is limited to four subcenters, potentially introducing regional bias.
Provenance
Source
figshare, authored by Lina Pang.
Collection Method
Designed as a clinical trial protocol for a multicenter, randomized, sham-controlled study.
Time Range
Trial includes a 3-week treatment period and follow-ups at 8 and 20 weeks post-intervention.
Freshness
Protocol last updated on 2026-03-25.
Geography
Study conducted across four subcenters; specific locations not detailed.
File is a PDF study protocol, not tabular data. The CC BY 4.0 license allows sharing and adaptation with attribution.