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Analysis of anxiety factors and intervention measures for patients undergoing cesarean section operation

Analysis of anxiety factors and intervention measures for patients undergoing cesarean section operation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116933
Enrollment
Unknown
Registered
2026-01-16
Start date
2022-06-03
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Anxiety before cesarean section

Interventions

Control group:Patients undergoing cesarean section received a traditional preoperative visit one day before the surgery.
Psychological intervention group:Patients undergoing cesarean section received 30 minutes of preoperative video education and mindfulness meditation one day before the surgery.
Traditional Chinese Medicine Intervention Group:Patients undergoing cesarean section received 30 minutes of electro-stimulation at low and dense frequencies (2/10 Hz) through the skin acupoints one da
Joint Intervention Group:Patients scheduled for cesarean section received both preoperative video education and mindfulness meditation, along with 30 minutes of transcutaneous low-frequency dense-spar

Sponsors

Baoshan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age > 18 years old; 2. ASA classification 1-2 grade; 3. Planned to undergo cesarean section under subarachnoid block or combined spinal-epidural anesthesia; 4. Full-term (gestational age > 37 weeks) single fetus; 5. Has not received preoperative video education, mindfulness meditation, percutaneous acupoint electrical stimulation, medication, etc. before; 6. The research subjects must give informed consent and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1. Patients who have been taking psychotropic drugs for a long time or abusing alcohol or prohibited drugs; 2. Those with communication disorders; 3. Researchers who have participated in or are currently participating in similar studies; 4. Those who refuse to sign the consent form; 5. Those who do not wish to continue the experiment during the experiment period.

Design outcomes

Primary

MeasureTime frame
Self-rating Anxiety Scale score;Anxiety index ;Intraoperative hemodynamic monitoring;Visual analogue scale,VAS;Postoperative nausea and vomiting;Somnipathy;The number of analgesic drug additions;The incidence rate of supine position syndrome;Cumulative use of ondansetron;Pain index;

Secondary

MeasureTime frame
First time out of bed activity;First exhaust time;Time of first breastfeeding;Catheter retention time;Length of postoperative stay;Satisfaction with anesthesia;

Countries

China

Contacts

Public ContactYan Li

Baoshan People's Hospital

1453417968@qq.com+86 875 212 0063

Outcome results

None listed

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