Study Evaluating the Effect of Person-centred Care for Patients Admitted for Inpatient Care at an Internal Medicine Unit
29 oktober 2018 bijgewerkt door: Göteborg University
Person-centred Inpatient Care - a Quasi-experimental Study Within an Internal Medicine Context
Patients admitted to internal medicine care environments have complex care needs and must be treated as persons with resources and responsibilities.
Person-centred care is defined as care in which the caregiver aims to get to know the patient as a person, and the care comprises a holistic approach to assess patients' needs and resources.
There is strong motivation for future health care to transform into an approach that acknowledges and endorses every patient's resources, interests and needs.
There is limited existing research on the benefit of implementing person-centred care in internal medicine care environments for all patients regardless of diagnosis or care pathway.
Little is known about the effects of person-centred inpatient care on patients' satisfaction with care.
This study includes adult patients admitted to an internal medicine inpatient unit regardless of reason for admission.
The aim of the study is to evaluate effects of person-centred inpatient care on care processes, in terms of satisfaction with care and person-centred content in medical records and to evaluate effects on self-reported health and self-efficacy.
Studie Overzicht
Toestand
Voltooid
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Werkelijk)
177
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Gothenburg, Zweden, 41345
- Department of Medicine, Sahlgrenska University Hospital
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar en ouder (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- acute or elective admission with a minimum projected in-hospital stay of 24 hours
- age ≥ 18 years
- conscious and alert, with no delay in response.
Exclusion Criteria:
- cognitive impairment or a judgment by the caregivers that inclusion was not in the best interests of the patient (e.g. end of life care, impaired psychological wellbeing).
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Onderzoek naar gezondheidsdiensten
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Person-centred inpatient care
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The intervention comprises three sequential steps in the care process. The first two steps follow one after the other in conjunction with admission to the ward: 1) person-centred assessment, and 2) creation of a person-centred health plan. Persistent person-centred inpatient care, the third step, is practiced throughout the hospital stay, and is a component of the quality and patient safety program. The model is systematically applied to all patients admitted to the unit. All staff are trained in PCC before implementation of the intervention. |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Satisfaction with care comprise patients' evaluations of caregivers' identity-oriented approach and the sociocultural atmosphere at the ward.
Tijdsspanne: From date of admission until the date of discharge, up to 60 days of hospitalization.
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The outcome is assessed with the questionnaire Quality from the Patient Perspective.
The questionnaire comprises four dimension of with two dimensions is used: Identity-oriented approach (13 items) and the sociocultural atmosphere (5 items).
One item from the medical competence subscale (effective pain relief) and one additional item on provision of information about medications is also used.
Two kinds of assessments are being made at each item: whether things were being done (perceived reality) and whether the right things were being done (subjective significance).
For the primary outcome only the assessments of perceived reality are being used.
Items are rated on a four-point response scale ranging from 1 (do not agree at all) to 4 (completely agree).
Each item also has a response option of "not applicable".
Subscales can be reported item by item or combined in a subscale score (average of all responses within the subscale).
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From date of admission until the date of discharge, up to 60 days of hospitalization.
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Person-centred content in medical records
Tijdsspanne: From date of admission until the date of discharge, up to 60 days of hospitalization.
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Degree of person-centredness in medical records
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From date of admission until the date of discharge, up to 60 days of hospitalization.
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Self-reported health assessed with EQ-5D-5L
Tijdsspanne: at the date of discharge, an average of 5 days after inclusion
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Self-reported health is measured with the EuroQual-5Dimensions-5Levels questionnaire (EQ- 5D- 5L).
The questionnaire comprises 1 item per dimension.
The dimensions of importance for health which are included are; mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.
Patients rate each item on a scale ranging from 1 (no problems) to 5 (extreme problems/unable to).
A unique health state is defined by combining 1 level from each of the 5 dimensions.
The questionnaire also includes EQ-VAS, in which the patients grade their current health status on an analogue scale from 0 (worst health) to 100 (best health).
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at the date of discharge, an average of 5 days after inclusion
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Physical and psychological wellbeing assessed with the Quality from the Patient Perspective questionnaire
Tijdsspanne: at the date of discharge, an average of 5 days after inclusion
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Patients rated their physical and psychological wellbeing on two separate five-point Likert scales ranging from "very good" (5) to "very bad" (1).
These two items are included in the Quality from the Patient Perspective questionnaire as two separate questions.
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at the date of discharge, an average of 5 days after inclusion
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Level of general self-efficacy assessed with the General Self-Efficacy scale
Tijdsspanne: at the date of discharge, an average of 5 days after inclusion
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General self-efficacy measures confidence in one's ability to handle difficult challenges in life.
It includes 10 items, which are rated on a four- point Likert scale giving a summary score of 40 for the total scale (10-40).
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at the date of discharge, an average of 5 days after inclusion
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Quality of care measured with ratings of Medical-technical competence and physical conditions at the ward assessed with the questionnaire Quality from the Patient Perspective.
Tijdsspanne: From date of admission until the date of discharge, up to 60 days of hospitalization.
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The questionnaire comprises four dimension of with the two rational dimensions was used for this specific aim: medical- technical competence (4 items) and physical-technical condition (3 items).
Two kinds of assessments are being made at each item: whether things were being done (perceived reality) and whether the right things were being done (subjective significance).
For this secondary outcome the assessments of perceived reality is being used.
A four-point response scale ranging from 1 (do not agree at all) to 4 (completely agree) forms the basis of ratings, each item also had a response option of "not applicable".
Subscales can be reported item by item or combined in a subscale score (average of all responses within the subscale).
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From date of admission until the date of discharge, up to 60 days of hospitalization.
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Clinical observations of pulse rate
Tijdsspanne: From date of admission until the date of discharge, up to 60 days of hospitalization.
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Frequency of documented pulse rate during hospitalization.
The medical records are reviewed retrospectively.
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From date of admission until the date of discharge, up to 60 days of hospitalization.
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Quality of care assessed as documented information in medical records on current medication at a daily basis and at discharge
Tijdsspanne: From date of admission until the date of the discharge, up to 60 days of hospitalization.
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All information in the medical records during hospitalization are reviewed retrospectively.
Rating is made regarding the presence (yes or no) of information on current medication at a daily basis and at discharge.
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From date of admission until the date of the discharge, up to 60 days of hospitalization.
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Quality of care assessed as documented information in medical records on planned medical care at discharge.
Tijdsspanne: From date of admission until the date of discharge, up to 60 days of hospitalization.
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All information in the medical records during hospitalization are reviewed retrospectively.
Rating is made regarding the presence (yes or no) of information on planned medical care at discharge.
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From date of admission until the date of discharge, up to 60 days of hospitalization.
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Clinical observations of weight
Tijdsspanne: From date of admission until date of discharge, up to 60 days of hospitalization.
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Frequency of documented clinical observations of weight (kg) during hospitalization.
The medical records are reviewed retrospectively.
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From date of admission until date of discharge, up to 60 days of hospitalization.
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Clinical observations of blood pressure
Tijdsspanne: From date of admission until the date of discharge, up to 60 days of hospitalization.
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Frequency of documented clinical observations of systolic and diastolic blood pressure during hospitalization.
The medical records are reviewed retrospectively.
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From date of admission until the date of discharge, up to 60 days of hospitalization.
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Clinical observations of respiratory rate
Tijdsspanne: From date of admission until the date of discharge, up to 60 days of hospitalization.
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Frequency of documented clinical observations of respiratory rate during hospitalization.
The medical records are reviewed retrospectively.
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From date of admission until the date of discharge, up to 60 days of hospitalization.
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Body temperature
Tijdsspanne: From date of admission until the date of discharge, up to 60 days of hospitalization.
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Frequency of documented clinical observations of body temperature (degrees celsius) during hospitalization.
The medical records are reviewed retrospectively.
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From date of admission until the date of discharge, up to 60 days of hospitalization.
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Onderzoekers
- Hoofdonderzoeker: Eva Jakobsson Ung, Associate professor, Department of Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden and Institute of Health and Care Sciences, Sahlgrenska Academy at the University of Gothenburg
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
9 november 2015
Primaire voltooiing (Werkelijk)
30 juni 2016
Studie voltooiing (Werkelijk)
30 juni 2016
Studieregistratiedata
Eerst ingediend
16 oktober 2018
Eerst ingediend dat voldeed aan de QC-criteria
29 oktober 2018
Eerst geplaatst (Werkelijk)
31 oktober 2018
Updates van studierecords
Laatste update geplaatst (Werkelijk)
31 oktober 2018
Laatste update ingediend die voldeed aan QC-criteria
29 oktober 2018
Laatst geverifieerd
1 oktober 2018
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- Person-centred care
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
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