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A Pragmatic Randomized Controlled Trial on Acupuncture Intervention to Alleviate Multifaceted Psychosomatic Comorbidities Among Breast Cancer Patients Based on Shared Decision-Making Model

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• 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;

• Clear consciousness, basic communication ability, and capacity to complete scale assessments cooperatively;

• Voluntary written informed consent signed by the patient or legal representative.

Locations
Other Locations
China
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
RECRUITING
Tianjin
Tianjin Academy of Traditional Chinese Medicine Affiliated Hospital
RECRUITING
Tianjin
Tianjin Medical University Cancer Institute and Hospital
RECRUITING
Tianjin
Contact Information
Primary
LI LI, Doctor of Philosophy
lilitcm@foxmail.com
18222626653
Time Frame
Start Date: 2026-08-01
Estimated Completion Date: 2028-03-31
Participants
Target number of participants: 216
Treatments
Experimental: Acupuncture group
Acupuncture、Auricular point pressing
No_intervention: routine nursing control group
Related Therapeutic Areas
Sponsors
Collaborators: Tianjin Academy of Traditional Chinese Medicine Affiliated Hospital, Tianjin Medical University Cancer Institute and Hospital
Leads: First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

This content was sourced from clinicaltrials.gov