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Impact of an Educational Program in the Management of Community-Acquired Pneumonia

Impact of an EDUcational program in the management of Community-Acquired Pneumonia: a prospective randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN39531840
Enrollment
204
Registered
2009-09-18
Start date
2011-11-01
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Community-acquired pneumonia Respiratory Viral pneumonia, not elsewhere classified

Interventions

Patients will be randomly assigned to receive the educational program during hospitalisation to improve their own understanding of the disease and self-care management at home. The control group will

Sponsors

Institute of Biomedical Investigations of Bellvitge (Institut d'Investigació Biomèdica de Bellvitge) (IDIBELL) (Spain)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult patients (aged 18 years and over), either sex 2. Diagnosed with community-acquired pneumonia 3. Requiring hospitalisation in the Infectious Diseases and Respiratory Departments of Hospital Universitari de Bellvitge Updated 05/09/2014: 3. Requiring hospitalisation in the Infectious Disease or Respiratory Disease Departments of Hospital Universitari de Bellvitge, Respiratory Disease Department or Home-care Service of Hospital Clínic de Barcelona and Respiratory Disease or Internal Medicine Departments of Hospital Universitari Arnau de Vilanova de Lleida

Exclusion criteria

Exclusion criteria: 1. Derived from a nursing home or extended care facility 2. Cognitive deficit 3. Do not understand Spanish or Catalan languages 4. No signed informed consent Added 05/09/2014: 5. Immunocompromised patients

Design outcomes

Secondary

MeasureTime frame
1. Patient satisfaction 2. Time to return to normal activities 3. Intermediate objectives of the educational program To achieve the variables all patients will be followed up a month after discharge. At 3 months, we also will assess the educational program through a telephone call. All variables will be collected in a Statistical Package for the Social Sciences (SPSS) database.

Primary

MeasureTime frame
1. Epidemiological, clinical and evolutive characteristics during the admission 2. Healthcare resources utilisation (readmissions and consultations to primary care and emergency department) within 30 days subsequent to discharge We will conduct a complete medical history to obtain epidemiological, clinical and evolutionary variables during the hospitalisation. To achieve the variables related to the healthcare resource utilisation, all patients will be followed up a month after discharge. All variables will be collected in a Statistical Package for the Social Sciences (SPSS) database.

Countries

Spain

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 4, 2026