Analysis of Multimodal Psychosomatic Comorbidity Burden in Breast Cancer and Benefit Evaluation of Acupuncture Collaborative Management Regimen

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-70
SponsorFirst Teaching Hospital of Tianjin University of Traditional Chinese Medicine

About this trial

This study adopts a multicenter, pragmatic, umbrella randomized controlled trial design integrated with the shared decision-making (SDM) model. Patients are stratified into four subgroups based on their core psychosomatic symptom phenotypes (single symptom vs. multiple comorbid symptoms). Participants are randomly assigned to the intervention group or control group at a 2:1 allocation ratio. For the intervention group, personalized interventions (including manual acupuncture, auricular point pressing, and combined manual acupuncture plus auricular point pressing) are selected via shared decision-making between clinicians and patients, while the control group receives routine nursing care. The study evaluates the improvement efficacy of single symptoms and the synergistic relief effect of multiple co-occurring symptoms across all psychosomatic phenotype subgroups under the shared decision-making framework. This design addresses the limitation of conventional randomized controlled trials that only focus on individual symptoms, and better fits real-world clinical scenarios characterized by multimorbid coexistence.

Eligibility criteria

Qualifiers

Female patients aged 18 to 70 years old;

Patients with pathologically or cytologically confirmed breast cancer;

Meeting at least one diagnostic criterion for psychosomatic symptoms:Anxiety or depressive state: subscale score of anxiety or depression on the HADS ≥ 8;Sleep disturbance: total score of the PSQI ≥ 8;Cancer-related fatigue: total score of the BFI ≥ 4;

Expected survival time ≥ 1 year;

Disqualifiers

Patients with severe mental disorders (such as schizophrenia and bipolar disorder) or lacking civil capacity;

Ineligibility for auricular point pressing intervention: local auricular skin breakage, infection, or allergic constitution (allergy to vaccaria seeds or adhesive plasters);

Patients receiving other acupuncture or acupoint pressing interventions, or those unable to discontinue such treatments during the trial period;

Patients unsuitable for manual acupuncture, including those with bleeding tendency (e.g., coagulation disorders, purpura) or local skin lesions at acupoint sites;

Trial design

Treatments tested in this trial

  • Acupuncture

Treatment groups

216 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

Lead sponsor

Tianjin Medical University Cancer Institute and Hospital

Collaborator

Tianjin Academy of Traditional Chinese Medicine Affiliated Hospital

Collaborator