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Continuing Education Intervention Named "Person First - Please"

NCT04833153 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2022-11-10

No results posted yet for this study

Summary

The aim of this study is to evaluate the effectiveness of the Person-First - Please (PFP) intervention in supporting nurse's competence and collective competence of Person-Centred Care (PCC) in older people Long-Term Care (LTC). The goal is to promote PCC culture in older people LTC.

Research question 1:

What is the effectiveness of the PFP intervention on the PCC collective competency of nurses in older people LTC?

Hypothesis for research question 1 are:

1\. Nurses in intervention group will have higher level of competence of PCC than control.

Research question 2:

How PCC climate has been maintained in older people LTC from the point of view of the nurses, next of kin and older people?

Hypothesis for research question 2 are:

1. PCC climate will be better in intervention group than control from point of view of the nurses, next of kin and older people.
2. The higher competence of nurses the higher level of PCC climate from point of view of the next of kin and older people.
3. The higher collective competence of the nurses the higher level of the PCC climate from point of view of the next of kin and older people.

Conditions

  • Nurse-Patient Relations

Interventions

BEHAVIORAL

Person-First - Please (PFP)

PFP takes 10 weeks and consist of four modules: Information, Person, Autonomy and Dignity. Information module takes 1 hour contact on first week. The other modules will follow every third weeks, starting from week 2. So that on week 2, 5 and 8 researcher meet nurses in 4 hours education session. Between the modules, nurses can take contact online to the researcher.

Sponsors & Collaborators

  • Mari Pakkonen

    lead OTHER

Principal Investigators

  • Suhonen, Professor · University of Turku

Study Design

Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Max Age
110 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-30
Primary Completion
2022-01-02
Completion
2022-03-31

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04833153 on ClinicalTrials.gov