Data Sheet 1_Acupuncture for irritable bowel syndrome comorbid with anxiety and depression
by Xuezhou Wang·Updated 1mo ago
32.6 KB1files
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Description
A 32.6 KB study protocol document outlines a placebo run-in, randomized controlled trial investigating acupuncture for irritable bowel syndrome (IBS) patients with comorbid anxiety and depression. The protocol, authored by Xuezhou Wang and published on figshare in 2026, details a trial with 80 eligible patients, a 4-week intervention, and an 8-week follow-up period. Primary and secondary outcomes include the IBS Symptom Severity Scale (IBS-SSS), Hospital Anxiety and Depression Scale (HADS), and safety monitoring.
Use Cases
Analyzing clinical trial design and outcome measures based on the described IBS-SSS and HADS endpoints.
Studying placebo response exclusion methods based on the described sham acupuncture run-in period.
Examining safety and blinding assessment protocols for acupuncture interventions as detailed in the trial methods.
Strengths
The protocol is clearly structured with defined primary and secondary outcomes, including IBS-SSS and HADS scores.
The trial design includes a placebo run-in period to exclude strong placebo responders, a specific methodological strength.
The document is licensed under CC-BY-4.0, allowing for open sharing and reuse.
Limitations
The dataset is a 32.6 KB DOCX file containing a study protocol, not the underlying clinical trial data itself.
Row count and column-level documentation for any potential data are absent; field semantics must be inferred after download.
The description metadata is limited to the protocol summary; actual data quality requires manual inspection.
Provenance
Source
figshare, authored by Xuezhou Wang.
Collection Method
Likely a manually authored study protocol document for a planned clinical trial.
Time Range
The protocol describes a future trial; temporal coverage of any resulting data is not specified.
Freshness
Last updated 2026-04-22 05:46:22; freshness should be verified.
Geography
Geography is not specified in the provided metadata.
The file is a DOCX document (study protocol), not a structured data file like CSV. The underlying trial data is not included.