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A randomized controlled trial on the effect of different preoperative interventions during the perioperative period on the incidence of postoperative sleep disorders in female patients undergoing laparoscopic surgery

A randomized controlled trial on the effect of different preoperative interventions during the perioperative period on the incidence of postoperative sleep disorders in female patients undergoing laparoscopic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115346
Enrollment
Unknown
Registered
2025-12-24
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Perioperative sleep disorder

Interventions

Doctor intervention group:The day before the surgery, the doctor prepares the subjects for preoperative education, informs the anesthesia surgery process, teaches the subjects sleep hygiene, informs t
AI intervention group:One day before the operation, the subjects were informed that they could search for content such as preoperative education, anesthesia and operation procedures, sleep hygiene edu

Sponsors

Shaanxi Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Female patients undergoing laparoscopic surgery; 2. Surgical patients aged 18-65; 3. The American Society of Anesthesiologists (ASA) physical status is graded I-III; 4. Body mass index (BMI) 18-30kg/m^2; 5. Good compliance, willing to accept this therapy;

Exclusion criteria

Exclusion criteria: 1. The patient refused to participate in the study. 2. Body mass index (BMI) > 30kg/m^2; 3. Presence of pre-operative conditions that affect sleep, such as neurological disorders, endocrine disorders, psychiatric disorders, or chronic pain that the researchers believe may interfere with the evaluation of the study. 4. Insomnia Severity Index (ISI) >= 8 or other preoperative sleep disorders such as obstructive sleep apnea, periodic limb movement disorder, restless legs syndrome, circadian rhythm disorder, or narcolepsy; 5.A recent history of drug abuse; 6. Presence of cognitive impairment or inability to communicate; 7. Patients with severe complications such as severe allergic reactions or massive bleeding during surgery who require rescue; 8. Use of hypnotic drugs during postoperative follow-up; 9. Do not use patient-controlled intravenous analgesia (PCIA); 10. Failure to complete the study program or to lose patients for various reasons during follow-up; 11. Those with a history of alcoholism or excessive consumption of coffee or strong tea; 12. Participate in other clinical investigators.

Design outcomes

Primary

MeasureTime frame
Incidence rate of postoperative sleep disorders;

Secondary

MeasureTime frame
Visual Analogue Scale;Hospital Anxiety and Depression Scale;Incidence rate of postoperative complications;

Countries

China

Contacts

Public ContactJiangjing Li

Shaanxi Provincial People's Hospital

lulu2790@163.com+86 180 9271 2790

Outcome results

None listed

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