Efficacy of TEAS and Acupressure for Breast Cancer Chemotherapy Adverse Reactions
by Jiang Yuan·Updated 2mo ago
57.2 KB1files
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Description
198 breast cancer patients receiving chemotherapy were randomized into control, transcutaneous electrical acupoint stimulation (TEAS), and acupressure groups for a longitudinal follow-up over four chemotherapy cycles. The dataset, authored by Jiang Yuan and last updated in April 2026, contains results from a clinical trial analyzing the dynamic effects of these non-invasive interventions on symptoms like nausea, vomiting, anxiety, and sleep disorders. Analysis was performed using generalized estimating equations (GEE), intention-to-treat (ITT), and per-protocol set (PPS) methods.
Use Cases
Compare the efficacy of TEAS versus acupressure for reducing chemotherapy-induced nausea and vomiting based on longitudinal symptom tracking.
Model the temporal dynamics of anxiety and depression symptoms across chemotherapy cycles based on the described intervention effects.
Analyze the cumulative therapeutic effect of TEAS on quality of life and sleep quality during mid-to-late chemotherapy stages.
Evaluate intervention strategies for personalized symptom management in breast cancer patients based on the distinct effect profiles described.
Strengths
Data from a randomized clinical trial with 198 participants, providing a structured experimental basis.
Longitudinal design tracking patients over four full chemotherapy cycles, allowing analysis of dynamic effects.
Analysis includes both intention-to-treat and per-protocol set methodologies, which may enhance robustness.
Limitations
Column-level documentation is absent; field semantics must be inferred after download.
Row count is unknown, which may limit suitability assessment.
The dataset is 57.2 KB, indicating a very limited scope, likely containing summary results rather than raw patient-level data.
Provenance
Source
Clinical trial registered at Chinese Clinical Trial Registry (ChiCTR2300077667), shared via figshare.
Collection Method
Randomized clinical trial with simple randomization using R4.4.2 software.
Time Range
Temporal coverage of the study is not specified in the provided metadata.
Freshness
Last updated 2026-04-15 04:37:17; freshness should be verified.
Geography
Spatial coverage is not specified in the provided metadata.
Primary data file is a DOCX document, which may require parsing to extract structured information.