Skip to content

Effect of a Transitional Care Intervention

Effect of a Transitional Care Intervention From Hospital to Home on Readmissions Among Older Medical Patients: a Quasi-experimental Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04796701
Enrollment
1266
Registered
2021-03-15
Start date
2017-02-01
Completion date
2019-12-31
Last updated
2021-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frailty

Keywords

readmission, transitional care, discharge, older medical patients

Brief summary

The objective of this study is to evaluate the effect of a transitional care intervention on readmissions among older medical patients. The proportion of older people is rapidly growing. These changes represent a challenge for healthcare systems. 20% of all hospital admitted patients ≥ 65 years are readmitted within the first 30 days after discharge. Prior transitional care research has mainly focused on either hospital-based or community-based interventions with no or little intervention elements in both settings. The results show different effects on readmission rates. This calls for new research on trans-sectorial interventions with both pre- and post-discharge elements.

Detailed description

Design: Non-randomized controlled trial. Participants For eligibility criteria - see elsewhere. Intervention group • Patients living in Odder, Skanderborg or Hedensted municipality Control group • Patients living in Horsens municipality Follow-Home Intervention The intervention group receives following intervention: If possible, all included participants are physically followed home by a hospital-based project worker on the day of discharge. During the visit, the focus is on: basic human needs, medication review reconciliation, and a comprehensive geriatric assessment. Problems, challenges and concerns are discussed. Finally, a conference for the following working day is arranged either as a physical visit or a video conference. The patient, relatives, community-based nurse and project worker are invited to participate and health status and challenges are discussed They are recommended to contact the project worker about health and practical issues up to 7 days after discharge where the intervention ends. Subsequently, the responsibility for treatment and care is assigned to the GP and home healthcare provider. Usual care Patients in the control group recieves the following usual discharge procedure: On the day of discharge, the hospital-based nurse digitally sends a summery of the hospital stay and a treatment and care plan to the community-based nurse. If needed, the hospital-based nurse contacts the community-based nurse by phone as a supplement to the plan. Finally, a discharge letter conducted by the hospital-based doctor is digitally sent to the GP. Method: Inclusion of participants is consecutive. Inclusion period was between 01/02/17 to 31/12/19. In total, approximately 1200 patients were included . Data collection Outcome data will be retrieved from CROSS-TRACKS database at 30 days after discharge from index admission. Analysis Intervention and Control group will be matched on 3 variables on individual level: * CCI * Index admission period: +/- 3-4 weeks * Sex All readmissions are included in the analysis (not only first time readmissions). That means that one patient can be included several times. Logistic regression adjusted for possible confounders will be used when analysing the outcomes. Confounders are chosen through a study specific DAG. Sub-group analysis will be conducted according to: * Age * Sex * Housing * Civil status * Social status * Length of hospital stay in index admission * Comorbidity * Diagnosis * Ect.

Interventions

OTHERFollow-Home-intervention

x

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Masking description

Intervention group: living in three predefined municipality Control group: living in one predefined municipality

Intervention model description

Non-randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
75 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged ≥75 years * Living in the municipalities of Odder, Skanderborg, Hedensted or Horsens * Admitted for ≥48 hours * Discharged from Medical Ward 1 (MSA1) at Horsens Regional Hospital (HRH)

Exclusion criteria

* Terminally ill patients * Patients with cerebrovascular events * Readmitted to another hospital * Not able to speak and understand Danish

Design outcomes

Primary

MeasureTime frameDescription
ReadmissionReadmission will be assessed at 30 days after hospital discharge in both intervention and control groupUnplanned all-cause readmission

Secondary

MeasureTime frameDescription
MortalityMortality will be assessed at 30 days after hospital discharge in both intervention and control groupAll-cause mortality

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026