Postoperative Sleep Disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ASA Class I-III; gynecological laparoscopic surgery; voluntary participation and signed informed consent
Exclusion criteria
Exclusion criteria: Patients with combined arrhythmias; those with pacemakers or other implantable electronic devices; individuals taking anticoagulant medications; those allergic to metal instruments; patients with infections, scars, or sensory impairment on the palmar side of the wrist; cognitive dysfunction impairing communication; Pittsburgh Sleep Quality Index (PSQI) scores above 5 on the first day before surgery; history of medication abuse within the past two months; and patients refusing to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Prevalence of sleep disturbances on day 1 after surgery; | — |
Secondary
| Measure | Time frame |
|---|---|
| The incidence of sleep disturbances on the second, third and seventh days after surgery;Pain scores (rest and exercise VAS scores) on days 1, 2, 3 and 7 after surgery;Incidence of nausea and vomiting;Anxiety and depression scores (HADS scale);The recovery assessment was conducted on the 7th day after surgery using 15 items of recovery quality; | — |
Countries
China
Contacts
Tumor Hospital Affiliated to Nantong University, Nantong Tumor Hospital