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CompletedNCT06945991Updated Apr 27, 2025

Application and Effect Evaluation of Integrated Nursing and Medical Management in Pediatric Lobar Pneumonia

An observational study in Pediatrics, Lobar Pneumonia and Inflammatory Markers, sponsored by Children's Hospital of Hebei Province. Completed at 1 site in China. Open to participants aged 1 Year to 12 Years. Per ClinicalTrials.gov, last updated 2025-04-27.

Sponsored by Children's Hospital of Hebei Province · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
50
Ages
1 Year to 12 Years
Sex
All
01

Study summary

Integrated nursing and medical management significantly improves clinical symptoms and pulmonary function in children with lobar pneumonia, shortens hospitalization duration, reduces complication rates, and enhances caregiver satisfaction. These findings support its broad clinical applicability and value.

Read the detailed description

This study aims to evaluate the clinical efficacy of integrated nursing and medical management in the treatment of pediatric lobar pneumonia. Specifically, it assesses its impact on symptom relief, pulmonary function recovery, inflammatory response control, duration of hospitalization, and caregiver satisfaction. Fifty pediatric patients diagnosed with lobar pneumonia and admitted to our hospital between January and December 2023 were selected and randomly assigned to either the observation group or the control group (n = 25 each) using a random number table. The control group received routine nursing care, while the observation group was additionally managed with an integrated nursing and medical approach. The two groups were compared in terms of duration of fever, cough, pulmonary rales, antibiotic treatment, length of hospital stay, pulmonary function parameters (FEV₁, FVC, FEV₁/FVC), inflammatory markers (CRP, WBC, PCT, LDH), overall treatment efficacy, caregiver satisfaction, and incidence of adverse events.

02

Conditions studied

  • Pediatrics
  • Lobar Pneumonia
  • Inflammatory Markers
  • Satisfaction

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03

In context

Pneumonia

2,044 studies on the registry are indexed under Pneumonia; 283 are open to participants now.

This study's enrollment of 50 is below the median of 203 across 688 observational studies indexed under Pneumonia.

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Lead sponsor

Children's Hospital of Hebei Province is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Year to 12 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Fifty pediatric patients diagnosed with lobar pneumonia and admitted to our hospital between January and December 2023 were selected and randomly assigned to either the observation group or the control group (n = 25 each) using a random number table.

Inclusion criteria

  • (1) Met the diagnostic criteria for lobar pneumonia, presenting with symptoms such as fever, cough, and pulmonary rales, and confirmed by laboratory tests and chest X-ray;
  • (2) Aged between 1 and 12 years;
  • (3) Informed consent was obtained from the child's legal guardians.

Exclusion criteria

Exclusion Criteria:

  • (1)Presence of other concurrent respiratory diseases;
  • (2) Congenital or acquired airway malformations, or airway foreign bodies;
  • (3) Impaired hepatic or renal function;
  • (4) Presence of other systemic diseases;
  • (5) Cognitive impairment.
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
50 participants (actual)
Patient registry
No

Groups and cohorts

  • control group

    The control group received routine nursing care

    Other: control group

  • observation group

    the observation group was additionally managed with an integrated nursing and medical approach.

    Other: observation group

Interventions

  • Otherobservation group

    the observation group was additionally managed with an integrated nursing and medical approach.

  • Othercontrol group

    The control group received routine nursing care

06

What researchers measure

Primary outcomes

  1. Time to Clinical Resolution of Symptoms

    Duration (in days) from hospital admission until resolution of three key symptoms: fever (axillary temperature \<37.3°C for 24h), cough (absence of cough for 48h), and pulmonary rales (absence on auscultation). Assessed daily by blinded clinicians.

    Time frame: From admission until discharge (up to 14 days).

Secondary outcomes

  1. Change in Pulmonary Function (FEV₁, FVC, FEV₁/FVC)

    Absolute change in spirometry-measured FEV₁ (L), FVC (L), and FEV₁/FVC ratio (%) from admission to discharge. Assessed using standardized spirometry protocols.

    Time frame: Baseline (T0) and discharge (T1; up to 14 days).

  2. Reduction in Inflammatory Markers (CRP, PCT, WBC, LDH)

    Percent reduction in serum CRP (mg/L), PCT (ng/mL), WBC (×10⁹/L), and LDH (U/L) levels from admission to discharge.

    Time frame: Baseline (T0) and discharge (T1; up to 14 days).

  3. Length of Hospital Stay

    Total days from admission to discharge, documented from electronic health records.

    Time frame: Up to 14 days.

  4. Parental Satisfaction Rate

    Proportion of caregivers reporting "very satisfied" or "satisfied" on a 4-point Likert scale (very satisfied/satisfied/neutral/dissatisfied) at discharge.

    Time frame: At discharge (T1; up to 14 days).

Other outcomes

  1. Incidence of Complications

    Proportion of patients experiencing adverse events (e.g., hemoptysis, pneumothorax, bronchospasm) during hospitalization, verified by imaging/lab reports.

    Time frame: From admission to discharge (up to 14 days).

  2. Antibiotic Usage Duration

    Total days of intravenous/oral antibiotic therapy, recorded from medication logs.

    Time frame: From admission to discontinuation (up to 14 days).

  3. Adherence to Rehabilitation Protocols

    Compliance with respiratory exercises (e.g., % of scheduled postural drainage sessions completed), tracked via nursing logs.

    Time frame: Daily during hospitalization (up to 14 days).

07

Study locations

1 site
  • Hebei Children's Hospital
    Shijiazhuang, 050000, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 27, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06945991
Lead sponsor
Children's Hospital of Hebei Province
Responsible party
Linlin Liu (Principal Investigator, Children's Hospital of Hebei Province) — Principal investigator
First posted
Apr 27, 2025
Start date
Jan 13, 2023
Primary completion
Mar 20, 2024
Completion
Oct 18, 2024
Last update
Apr 27, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

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