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Effect of mindfulness meditation training on the management of anesthesia in perioperative patients

Effect of mindfulness meditation training on the management of anesthesia in perioperative patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082405
Enrollment
Unknown
Registered
2024-03-28
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Perioperative patient anesthesia management

Interventions

Control group:Listen to the book twice a day for 20 min
Experimental group:Listen to meditation sessions twice a day for 20 min

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) Both men and women, aged 18 to 55 years old, proposed; diagnosed with chronic cholecystitis or chronic appendicitis (and the operation time is not less than 3 months); (2) The ASA grade is from grade I to grade II; (3) High school degree or above, able to understand the meaning of the scale; (4) The patient is healthy and has no serious underlying diseases; (5) To voluntarily participate in this treatment, and agree to sign the relevant treatment informed consent form.

Exclusion criteria

Exclusion criteria: (1) A history of severe physical illness and mental illness; (2) Serious risk of increased blood pressure or intracranial pressure; (3) poorly controlled or untreated hypertension (arterial hypertension, systolic / diastolic blood pressure over 180 / 100 mmHg at rest); (4) patients with serious arrhythmia (rapidity, ventricular tachycardia, ventricular early); (5) Pregnant women and female women prepared for pregnant women; (6) Subjects who are unable to understand the content of the relevant scale; (7) Subjects with adverse hazard factors deemed unfavorable by the investigator to participate in the trial; (8) Patients with severe underlying diseases (such as active cancer); (9) unwilling to cooperate with meditation training.

Design outcomes

Primary

MeasureTime frame
The amount of sedative and analgesic used;Time required for postoperative waking to extubation;Incidence of adverse effects after extubation;Vital signs (blood pressure, heart rate, blood oxygen, respiratory rate) before entering the operating room, 10min, and 5 min after extubation;The amount of opioid analgesia with intravenous controlled analgesia (PCIA);

Secondary

MeasureTime frame
Post-operative pain score;

Countries

China

Contacts

Public ContactWenyuan Wang

Zhejiang Provincial People's Hospital

Neuro-anesth@hotmail.com+86 135 8808 3716

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026