Evaluating pain management education for children after surgery
Evaluation of Post-PACU Pain Management Experiences in Pediatric Ambulatory Surgery Patients
This study tests if teaching kids about pain management after surgery helps them feel better and recover more smoothly compared to standard care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 900 (estimated) |
| Ages | 1 Year to 6 Years |
| Sex | All |
| Sponsor | Columbia University Academic / other |
| Locations | 1 site (New York, New York) |
| Trial ID | NCT02352116 on ClinicalTrials.gov |
What this trial studies
This study assesses the impact of additional education on pain management for children recovering from ambulatory surgery. It compares two groups: one receiving face-to-face education about postoperative pain expectations and management, and the other receiving standard care. The study evaluates pain severity and satisfaction through parental reports and questionnaires at multiple time points post-surgery. Additionally, it examines behavioral changes in children during recovery to understand how these may influence their overall postoperative experience.
Who should consider this trial
Good fit: Ideal candidates are children aged 1-6 years undergoing ambulatory surgical procedures with ASA status I or II.
Not a fit: Patients with ASA status III or IV, or those requiring inpatient recovery, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve postoperative pain management and satisfaction for pediatric patients and their families.
How similar studies have performed: Other studies have shown that educational interventions can improve pain management outcomes in pediatric populations, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients ages 1-6 years undergoing ambulatory surgical procedures. * Patients with an ASA status of I or II spending 23 hours or less recovering in the PACU and discharged home. Exclusion Criteria: * Patients with an ASA status of III or IV. * Patients admitted as inpatients or transferred to the PICU or inpatient for recovery, and any conditions that may affect pain expression or sensation.
Where this trial is running
New York, New York
- Columbia University — New York, New York, United States (Recruiting)
Study contacts
- Principal investigator: Lena S. Sun, MD — Columbia University
- Study coordinator: Lena S. Sun, MD
- Phone: 212-305-2413
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.