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Development and Preliminary Application of a Child Life Model-Based Intervention Protocol for Perioperative Stress Responses in Children Aged 3-12 Years with Pneumonia Undergoing Bronchoalveolar Lavage

Development and Preliminary Application of a Child Life Model-Based Intervention Protocol for Perioperative Stress Responses in Children Aged 3-12 Years with Pneumonia Undergoing Bronchoalveolar Lavage

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113948
Enrollment
Unknown
Registered
2025-12-04
Start date
2025-12-31
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Pneumonia

Interventions

Intervention group:Intervention for Perioperative Stress Responses in Children Aged 3-12 Years with Pneumonia Undergoing Bronchoalveolar Lavage Based on the Child Life M

Sponsors

The Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Age: 3 to 12 years old; 2. The child was diagnosed with pneumonia; 3. First-time BAL treatment, or at least 3 months since the last BAL treatment; 4. All pediatric patients will be included regardless of whether they exhibit a stress response. 5. The child's guardian understands the study content and can communicate effectively in Chinese. The child possesses basic verbal communication skills or nonverbal expression abilities, is able to cooperate with symptom assessments, and voluntarily participates in the study.

Exclusion criteria

Exclusion criteria: 1. The parents of the pediatric patient refused to accept BAL treatment. 2. Children with severe underlying conditions or complications who are currently receiving palliative care; 3. Patients with active massive hemoptysis, severe bleeding disorders, coagulation disorders, severe pulmonary hypertension, and conditions that may induce massive hemoptysis. 4. Patients with severe malnutrition who cannot tolerate surgery; 5. Performed BAL and foreign body removal for the pediatric patient; 6. Long-acting sedatives, analgesics, or anxiolytics were administered within 24 hours prior to BAL. 7. Emergency BAL is required immediately; there is no time for preoperative Child Life intervention. 8. Participation in other clinical trials that may affect symptoms or intervention outcomes; 9. Patients transferred to another hospital or discharged early.

Design outcomes

Primary

MeasureTime frame
Level of Perioperative Anxiety in Children;

Secondary

MeasureTime frame
Level of Perioperative Anxiety in Children;Heart rate;Surgery time;Postoperative Pain Levels in Children;

Countries

China

Contacts

Public ContactBai Yongqi

The Affiliated Hospital of Southwest Medical University

13882787833@qq.com+86 138 8278 7833

Outcome results

None listed

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