Individualized preoperative education to reduce anxiety and improve recovery
Effect of Preoperative Individualized Education on Anxiety and Recovery in Patients Undergoing Minimally Invasive Lung Surgery
This study tests whether personalized pre-surgery education can help reduce anxiety and improve recovery for patients having single-port thoracoscopic surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 156 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Fujian Medical University Union Hospital Academic / other |
| Locations | 1 site (Fuzhou, Fujian) |
| Trial ID | NCT06419088 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of personalized preoperative education on patients undergoing single-port thoracoscopic surgery. Participants will be randomly assigned to receive either individualized educational interventions using audiovisual materials or routine preoperative education. The study aims to assess levels of anxiety and postoperative recovery through questionnaires and scales measuring various symptoms and concerns. The goal is to determine if tailored education can enhance patient outcomes and quality of life post-surgery.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are scheduled for single-port thoracoscopic surgery.
Not a fit: Patients with mental disorders, preoperative pain, pregnancy, or other tumors requiring treatment may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce anxiety and improve recovery experiences for surgical patients.
How similar studies have performed: Previous studies have shown that individualized education can positively impact patient anxiety and recovery, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Aged 18 or above; 2. Received single-port thoracoscopic surgery; 3. Volunteered to participate in the study and signed an informed consent form. Exclusion Criteria: 1. Presence of a mental disorder 2. Preoperative pain 3. Pregnancy 4. Presence of other tumours requiring treatment.
Where this trial is running
Fuzhou, Fujian
- Fujian Medical University Union Hospital — Fuzhou, Fujian, China (Recruiting)
Study contacts
- Study coordinator: Maohui Chen, Prof
- Email: 757860733@qq.com
- Phone: 18659181171
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.