Precision intervention of TEAS and mindfulness breathing therapy on perioperative anxiety in tumor patients undergoing surgery: A multicenter randomized controlled clinical trial

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2600127771

Enrollment

Unknown

Registered

2026-07-07

Start date

2026-08-01

Completion date

Unknown

Last updated

2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perioperative anxiety

Interventions

K group:None

T+Z group:TEAS combined with mindfulness therapy

T group:TEANS

Z group:mindfulness therapy

Radical Thyroidectomy:none

Halsted Radical Mastectomy:none

radical hysterectomy:none

Laparoscopic Radical Resection for Colorectal Cancer:none

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Patients with ASA physical status classification I–III; (2) Patients scheduled for elective radical thyroidectomy, Halsted radical mastectomy, radical hysterectomy, or laparoscopic radical resection for colorectal cancer under general anesthesia.

Exclusion criteria

Exclusion criteria: Phase 1: (1) History of psychiatric illness; (2) Pregnant or breastfeeding women; (3) Known psychiatric illness; (4) Poor cooperation; (5) Intraoperative change of surgical procedure. Phase 2: (1) History of psychiatric illness; (2) Poor cooperation or language/communication barriers; (3) Change of surgical procedure; (4) Patients with a pacemaker; (5) Patients with a history of upper extremity nerve injury or spinal surgery; (6) Patients with skin infection near the acupoints or allergy to electrode pads.

Design outcomes

Primary

Measure	Time frame
State-Trait Anxiety Inventory?;	—

Secondary

Measure	Time frame
Intraoperative anesthetic dosage;Type of surgery;Surgery duration;Anesthesia duration;intraoperative analgesic dosage;Presence or absence of abdominal adhesions;Postoperative incisional pain;Time to first ambulation;Time to first flatus;Postoperative nausea and vomiting;Time to first oral intake ;Duration of urinary catheterization;Duration of drainage tube placement ;Adverse events related to analgesics;Postoperative sleep quality;Whether subsequent radiotherapy or chemotherapy is required;Surgical pathological results;Postoperative hospital stay;Hospitalization costs;Anxiety score ;	—

Measure

Time frame

Intraoperative anesthetic dosage;Type of surgery;Surgery duration;Anesthesia duration;intraoperative analgesic dosage;Presence or absence of abdominal adhesions;Postoperative incisional pain;Time to first ambulation;Time to first flatus;Postoperative nausea and vomiting;Time to first oral intake ;Duration of urinary catheterization;Duration of drainage tube placement ;Adverse events related to analgesics;Postoperative sleep quality;Whether subsequent radiotherapy or chemotherapy is required;Surgical pathological results;Postoperative hospital stay;Hospitalization costs;Anxiety score ;

—

Countries

China

Contacts

Public ContactJin Dan

The First Affiliated Hospital of Wenzhou Medical University

jindan13506666165@163.com+86 135 0666 6165

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026