Morbid obesity
Conditions
Interventions
Control group:Routine Post-Anesthesia Care
Experimental Group A:5-minute interval wake-up call with loved ones' recorded voices
Experimental Group B:Continuous Wake-Up by Loved One's Voice Recording
Sponsors
The First Affiliated Hospital of Chongqing Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Age 18–65 years; 2. Patients with BMI >= 30 scheduled for weight-loss surgery; 3. American Society of Anesthesiologists (ASA) physical status classification I–III; 4. Presence of a clearly identified primary caregiver (defined as the relative with the most frequent daily contact within one month prior to surgery, such as spouse, parent, or child); 5. Patients who provide informed consent and voluntarily participate in the trial.
Exclusion criteria
Exclusion criteria: 1. Individuals with severe cardiopulmonary dysfunction or psychiatric disorders; 2. Individuals with severe liver or kidney dysfunction; 3. Individuals with hearing impairment; 4. Individuals with a history of complications during the recovery phase from general anesthesia; 5. Individuals whose primary relatives are not locally available or unable to participate in audio recording; 6. Patients unable to cooperate in completing the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Wake-up time; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of Hypoxemia During the Awakening Phase;Postoperative pain level;Incidence of agitation during the recovery phase;Incidence of Mean Arterial Pressure Fluctuations; | — |
Countries
China
Contacts
Public ContactLuo Jing
The First Affiliated Hospital of Chongqing Medical University
Outcome results
None listed