Impact of Good Practice Guidelines on Evidence-based Practice and Nurses' Work Environment

April 21, 2022 updated by: Silvia Esteban, Parc de Salut Mar

Impact of the Implementation of Good Practice Guidelines on Beliefs-attitudes and Behavior in the Face of Evidence-based Practice and on the Perception of the Nurses' Work Environment

Evidence-based practice (EBP) has improved patient health outcomes. The work environment of nurses is a key element to improving the quality of care and to facilitate EBP, while also improving health outcomes.

The CCEC® / BPSO® program consists of the implementation of Good Practice Guides in health organizations in the Spanish territory, and is carried out through a training and participatory methodology, actively involving nurses in the process.

The present study tries to know if in the health organizations where the CCEC® / BPSO® program has been implemented, the perception of the nurses' working environment has improved, as well as their attitude towards evidence-based practice, with respect to organizations where this program has not been implemented.

Study Overview

Detailed Description

Quasi-experimental pre-post multicentre study with a non-equivalent control group, within the framework of the third cohort of the RNAO Good Practice Guidelines Implementation Program in Centers Committed to Care Excellence (CCEC® / BPSO®).

PARTICIPATING INSTITUTIONS:

Intervention group(IG): (institutions included in the third cohort of CCEC®):

Estructura de Gestión Integrada de Lugo, Cervo y Monforte de Lemos (Galicia), Hospital General Universitario Santa Lucía (Murcia), Xerencia de Xestión Integrada de A Coruña (Galicia), Hospital Guadarrama (Madrid), Hospital Universitari Germans Trias i Pujol (Cataluña), Hospital Regional Universitario de Málaga (Andalucía), Organización Sanitaria Integrada OSI Araba (Araba).

Control group(CG): Hospital Son Espases (Mallorca), Hospital Son Llàtzer (Mallorca), Hospital de Granollers (Barcelona), Hospital de Puigcerdà (Girona), Hospital d'Igualada (Barcelona), Hospital General Universitario de Alicante (Alicante), Hospital Comarcal de Vinaròs de Castellón de la Plana (Castellón), Hospital Clínic de Barcelona (Barcelona), Hospital Universitario de Fuenlabrada (Madrid), Hospital de la Santa Creu i Sant Pau (Barcelona).

To collect data, two validated questionnaires will be passed to all nurses in 7 health institutions where the RNAO Good Practice Guidelines Implementation Program begins (experimental group) and in 10 where it is not implemented (control group), both groups distributed throughout the Spanish territory. Basal data will be recorded before the beginning of the program and post intervention data will be recorded after one year.

Then the results will be compared to determine whether there are differences between nurses who work in the group of hospitals that have started the program with respect to those who work in other centers. The total duration of the project will be three years.

Study Type

Interventional

Enrollment (Actual)

1200

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • A Coruña, Spain, 15006
        • Xerencia de Xestión Integrada de A Coruña
      • Alicante, Spain, 03010
        • Hospital General Universitario de Alicante
      • Barcelona, Spain, 08036
        • Hospital Clinic
      • Barcelona, Spain, 08041
        • Hospital de la Santa Creu i Sant Pau
      • Lugo, Spain, 27003
        • Hospital Lucus Augusti
      • Murcia, Spain, 30202
        • Hospital General Universitario Santa Lucia
      • Málaga, Spain, 29010
        • Hospital Regional Universitario de Malaga
      • Palma De Mallorca, Spain, 07120
        • Hospital Universitari Son Espases
      • Palma De Mallorca, Spain, 08198
        • Hospital Son Llatzer
    • Araba
      • Vitoria Gasteiz, Araba, Spain, 01009
        • Organización Sanitaria Integrada (OSI) Araba
    • Barcelona
      • Badalona, Barcelona, Spain, 08916
        • Hospital Universitri Germans Tries i Pujol
      • Granollers, Barcelona, Spain, 08402
        • Hospital de Granollers
      • Igualada, Barcelona, Spain, 08700
        • Consorci Sanitari Anoia-Hospital Igualada
    • Castelló
      • Vinaròs, Castelló, Spain, 12500
        • Hospital Comarcal de Vinaròs
    • Girona
      • Puigcerdà, Girona, Spain, 17520
        • Hospital de Puigcerdà
    • Madrid
      • Fuenlabrada, Madrid, Spain, 28942
        • Hospital Universitario de Fuenlabrada
      • Guadarrama, Madrid, Spain, 28440
        • Hospital de Guadarrama

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

21 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

Nurses Work in the institutions participating in the study Acceptance to participate in the study

Exclusion Criteria:

Not be active

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Good Practice Guidelines group
Implementation of Good Practice Guidelines
Implementation of Good Practice Guidelines on the framework of the Best Practice Spotlight Organization in Spain (CCEC® / BPSO®), that allows a standardized methodology for providing care and registering indicators.
No Intervention: usual practices group
Not Implementation of Good Practice Guidelines, so working as the usual way

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in Nurses' work environment
Time Frame: baseline and 1 year
self reported perceived current work environment through the Practice Environment Scale-Nursing Work Index (PES-NWI) questionaire, with 31 Likert type questions (1: "Strongly Disagree" -> 4 "Strongly Agree"), including 5 sub-scales: Nurse participation in hospital affairs (8 questions); nursing foundations for quality of care (10 questions); nurse manager ability, leadership and support of nurses (5 questions); staffing and resource adequacy (4 questions); and collegial nurse-physician relationships (3 questions)
baseline and 1 year
change in Beliefs- attitudes and behavior in front of EBP
Time Frame: baseline and 1 year
self-reported Beliefs- attitudes and behavior in front of EBP, through the 60 Likert type questions (from 1: minimum agreement to 10: maximum agreement) of the Health Sciences-Evidence Based Practice questionnaire (HS-EBP), that are classified in 5 dimensions: Beliefs and attitudes, (12 items); Results from scientific research (14 items); Development of professional practice (10 items); Evaluation of results (12 items) and Barriers / Facilitators (12 items).
baseline and 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in Job satisfaction: Likert type question rating
Time Frame: baseline and 1 year
self-reported job satisfaction through a unique Likert type question rating 1: very unsatisfied; 5: very satisfied.
baseline and 1 year
change in Institutional attitude perceived by nurses in relation to nursing research
Time Frame: baseline and 1 year
self-reported 4 question rating: yes, not, unknown.
baseline and 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Silvia Esteban-Sepúlveda, IMIM (Hospital del Mar Medical Research Institute), Barcelona

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2018

Primary Completion (Actual)

November 30, 2019

Study Completion (Actual)

April 21, 2022

Study Registration Dates

First Submitted

December 10, 2019

First Submitted That Met QC Criteria

December 12, 2019

First Posted (Actual)

December 13, 2019

Study Record Updates

Last Update Posted (Actual)

April 22, 2022

Last Update Submitted That Met QC Criteria

April 21, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Not considered, since the data processing will be done on an aggregate basis.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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