Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
NCT06522529

Sumamos Excelencia Project: Implementation of Best Practices in Clinical Practice (Thrid Edition)

Led by Instituto de Salud Carlos III · Updated on 2024-07-26

400

Participants Needed

1

Research Sites

73 weeks

Total Duration

On this page

Sponsors

I

Instituto de Salud Carlos III

Lead Sponsor

T

The Spanish Centre for Evidence Based Nursing and Healthcare

Collaborating Sponsor

AI-Summary

What this Trial Is About

There is a gap between research and clinical practice, leading to variability in decision-making. Multifaceted implementation strategies are for improving implementation of best practices. Quasi-experimental, multicentre, before and after. Primary care, hospital units and nursing homes, and the patients attended at both. Implementation of evidence-based recommendations by application of a multifaceted implementation strategy (training, audit, context analysis, local strategies design, feedback, facilitation). Data will be collected at baseline and, during the first year of follow up, at months (4,8,12)

CONDITIONS

Official Title

Sumamos Excelencia Project: Implementation of Best Practices in Clinical Practice (Thrid Edition)

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • NHS units and nursing homes that voluntarily join the project.
  • Units providing direct patient care and committed to implementing evidence-based recommendations on hand hygiene plus at least one topic: pain, urinary incontinence, obesity prevention, breastfeeding, smoking cessation, falls, or pressure injury prevention.
  • Patients susceptible to pain of any age treated in acute or chronic care settings.
  • Patients 18 years or older with uncomplicated stress, urge, or mixed urinary incontinence with at least 7 days admission or care continuity up to 6 weeks.
  • Babies and preschool children up to 12 years old in good general health; children aged 2 to 12 must not have been overweight or obese in the year prior to baseline.
  • Lactating individuals and healthy neonates over 36 weeks gestation and 2500 g birth weight; support network members; postpartum period up to 6 months of baby's life.
  • Smokers aged 18 years or older.
  • Adults 18 years or older at risk of pressure injuries admitted to hospitals, nursing homes, or home care.
  • Adults 65 years or older or adults 18 years or older with walking problems due to neurological or traumatic conditions, medication, loss of strength, or drowsiness.
  • Health professionals caring for patients in participating units.
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Instituto de Salud Carlos III - Unidad de Investigación en Cuidados y Servicios de Salud

Madrid, Spain, 28029

Actively Recruiting

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Research Team

L

Leticia Bernués-Caudillo, PhD Candidate

CONTACT

E

Esther González-María, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

1

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