Table 3_Efficacy and safety of transcutaneous electrical acupoint stimulation and acupress
by Jiang Yuan·Updated 2mo ago
27.8 KB1files
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Description
Jiang Yuan's dataset contains results from a randomized clinical trial on 198 female breast cancer patients undergoing chemotherapy. The data, published on figshare in 2026, compares the effects of transcutaneous electrical acupoint stimulation (TEAS) and acupressure versus a control group over four chemotherapy cycles. It analyzes intervention effects on nausea, vomiting, sleep, anxiety, depression, and quality of life using generalized estimating equations.
Use Cases
Compare the longitudinal efficacy of TEAS versus acupressure based on the described multi-cycle follow-up.
Model the dynamic progression of chemotherapy-induced nausea and vomiting (CINV) risk based on the described time effect.
Analyze intervention effects on psychosomatic symptoms like anxiety and depression based on the described primary outcomes.
Assess the cumulative therapeutic effect of TEAS based on the described interaction effect in mid-to-late chemotherapy cycles.
Strengths
Data is from a randomized clinical trial with 198 participants, providing a structured experimental basis.
Analysis includes intention-to-treat and per-protocol set analyses, suggesting methodological rigor.
Longitudinal follow-up over four chemotherapy cycles captures dynamic effects.
Limitations
Column-level documentation is absent; field semantics must be inferred after download.
Row count is unknown, which may limit suitability assessment for specific modeling tasks.
The dataset is very small at 27.8 KB, indicating limited scope, likely containing summary results rather than raw patient-level data.
Provenance
Source
figshare, author Jiang Yuan.
Collection Method
Data collected via a randomized clinical trial (ChiCTR2300077667) with simple randomization using R4.4.2.
Time Range
Temporal coverage of the trial is not specified, but data reflects four chemotherapy cycles.
Freshness
Last updated 2026-04-15 04:37:17; freshness should be verified.
Geography
Spatial coverage is not specified, but the trial was registered on a Chinese clinical trial registry.
File format is DOCX, which may require specific tools for programmatic data extraction.