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The effect of psychological intervention on perioperative anxiety and postoperative recovery in patients undergoing laparoscopic total hysterectomy surgery

The effect of psychological intervention on perioperative anxiety and postoperative recovery in patients undergoing laparoscopic total hysterectomy surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086377
Enrollment
Unknown
Registered
2024-07-01
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

fibroid

Interventions

Psychological intervention group :During the perioperative period, the subjects were given friendly and detailed communication and education for 10 minutes, and then the subjects followed the teaching
routine management group:Routine

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients with uterine fibroids undergoing laparoscopic total hysterectomy; 2.Female, between 18 and 65 years; 3. ASA rating I-?; 4. BMI: 18-30kg/m^2.

Exclusion criteria

Exclusion criteria: 1. Patients who refuse to sign the informed consent; 2. Patients with preoperative mental diseases (including confirmed bidirectional affective disorder, schizophrenia, etc.); 3. Patients with serious basic diseases (such as cardiovascular and cerebrovascular diseases, respiratory diseases or abnormal liver and kidney functions); 4. Patients with chronic pain or recent sedative and analgesic drugs; 5. Patients who refuse to listen to music.

Design outcomes

Primary

MeasureTime frame
state anxiety inventory, SAI;

Secondary

MeasureTime frame
visual analogue scale, VAS;St. Mary's Hospital Sleep Questionnaire, SMH;

Countries

China

Contacts

Public ContactMaoyin Zhang

The Affiliated Hospital of Xuzhou Medical University

540072028@qq.com+86 159 5220 5566

Outcome results

None listed

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