NCT04253665

Brief Summary

The objective of this study is to estimate the effect size of a nursing discharge teaching intervention on multimorbid inpatients activation level, health confidence, readiness for hospital discharge, experience with discharge care and rate and time to 7-days readmission.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
225

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Aug 2020

Geographic Reach
1 country

3 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 23, 2020

Completed
13 days until next milestone

First Posted

Study publicly available on registry

February 5, 2020

Completed
6 months until next milestone

Study Start

First participant enrolled

August 13, 2020

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2021

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2021

Completed
Last Updated

November 8, 2021

Status Verified

November 1, 2021

Enrollment Period

1 year

First QC Date

January 23, 2020

Last Update Submit

November 5, 2021

Conditions

Keywords

Discharge teachingNursingMultimorbidity

Outcome Measures

Primary Outcomes (1)

  • Change in Patient Activation Measure (PAM)

    The patient activation measure (PAM) is a 13-item self-report questionnaire to measure patient activation level. Stages of activation are distributed as follows in the PAM items: items 1-2: believing an active role is important; items 3-8: having confidence and knowledge to take action; items 9-11: taking action; and items 12-13: continuing healthy behaviors under stress. PAM raw score can be calculated by adding all of the responses to the 13 questions. This score is then converted into an activation score ranging from 0 = no activation to 100 = high activation using a calibration table. Psychometric properties of the PAM in hospitalized multimorbid patients showed a satisfying reliability (Cronbach's alpha = 0.88) and a content validity index of 0.91.

    change from hospital admission to the day of discharge and 7-10 days after discharge

Secondary Outcomes (4)

  • Change in Health Confidence Score (HCS)

    change from hospital admission to the day of discharge and 7-10 days after discharge

  • Readiness for Hospital Discharge Scale-Short Form (RHDS-SF)

    At the end of the hospital stay, an average of 7-10 days after admission

  • Readmission rate and time to readmission

    7-10 days after discharge

  • Discharge Care Experiences Survey (DICARES)

    7-10 days after discharge

Study Arms (2)

Usual care

NO INTERVENTION

Discharge teaching is usually not delivered in a systematic or consistenly way, nor by relying on a particular intervention model.

Discharge teaching

EXPERIMENTAL

Receiving tailored discharge teaching by nurses during hospital stay.

Behavioral: Nursing discharge teaching

Interventions

Nurses will provide multimorbid seniors inpatients with teaching related to self-management to prepare them to be discharged home. The teaching delivery will be tailored to patients' activation level and priorities. The intervention begins by determining the level of activation at which patients are and identifying priorities to address related to patients' life situation. A Discharge Teaching Guide will be used by nurses to deliver the teaching and includes six domains of self-management. For each domain, nurses first report whether a priority has been identified and what intervention they have proposed to address it. Then for each domain, teaching objectives are described and differ according to the level of patient activation. These six domains of self-management are found in the patient-oriented discharge summary, which is a document for the patient that summarizes what has been addressed in discharge teaching.

Discharge teaching

Eligibility Criteria

Age50 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • chronic diseases or more
  • Being discharged home
  • Able to speak, read and write in French

You may not qualify if:

  • Insufficient capacity to consent assessed with the University of California San Diego Brief Assessment of Capacity to Consent (UBACC).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

Lausanne University Hospital (CHUV)

Lausanne, 1010, Switzerland

Location

EHC (Hôpital de Morges)

Morges, 1110, Switzerland

Location

eHnv (Etablissements hospitaliers du nord vaudois)

Yverdon-les-Bains, 1318, Switzerland

Location

Related Publications (2)

  • Pellet J, Weiss M, Mabire C. Evaluation of a theory-informed implementation of a nursing discharge teaching intervention for older adults. J Adv Nurs. 2023 Aug;79(8):3147-3159. doi: 10.1111/jan.15666. Epub 2023 Apr 4.

  • Pellet J, Weiss M, Zuniga F, Mabire C. Implementation and preliminary testing of a theory-guided nursing discharge teaching intervention for adult inpatients aged 50 and over with multimorbidity: a pragmatic feasibility study protocol. Pilot Feasibility Stud. 2021 Mar 17;7(1):71. doi: 10.1186/s40814-021-00812-4.

MeSH Terms

Conditions

Chronic Disease

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Cedric Mabire, Dr. Sc.

    Institute of Higher Education and Research in Healthcare, University of Lausanne

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: 2 group pre/post-intervention comparative design: 90 control patients will be recruited before the implementation of the intervention in study units. This recruitment will last approximately two months, according to the estimated turnout of patients in these units. After this control period, 30 other patients will be recruited to receive the intervention. In this sense, participants are assigned to one group or the other, depending on the phase of the study.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr.Sc.

Study Record Dates

First Submitted

January 23, 2020

First Posted

February 5, 2020

Study Start

August 13, 2020

Primary Completion

August 31, 2021

Study Completion

September 30, 2021

Last Updated

November 8, 2021

Record last verified: 2021-11

Data Sharing

IPD Sharing
Will not share

Locations