Follow Home Visits After Discharge

NCT02318680 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 545

Last updated 2015-01-12

No results posted yet for this study

Summary

The study aims to assess whether a follow home visit after discharge of frail elderly patients from Nykøbing Falster Hospital reduces the risk of readmission within 180 days.

Staff from the hospital ward identifies patients fulfilling the inclusion criteria and refers the patients to two project nurses at the hospital (follow home team). One of the project nurses gets the informed consent from the patient, or in case of a patient who is not able to give informed consent, from the family and general practitioner. The patient is then randomized to intervention (follow home visit after discharge) or control.

In the intervention group, the hospital project nurse and the patient meets with the municipal nurse in the patient's home on the same day the patient is being discharged from the hospital. During this visit the discharge from the hospital and the actual functioning of the patient in his own surroundings is reviewed, using a structured assessment.

Conditions

  • Discharge Planning
  • Readmission
  • Hospital
  • Frail Elderly Patients

Interventions

OTHER

Review of follow home visits after discharge from Nykøbing Falster Hospital

The intervention is follow home visits which is randomized and is an intervention that is assigned by the investigator.

Sponsors & Collaborators

  • Region Zealand

    collaborator OTHER
  • Nykøbing Falster County Hospital

    collaborator OTHER
  • Guldborgsund Municipality

    collaborator UNKNOWN
  • Lolland Municipality

    collaborator UNKNOWN
  • Vordingborg Municipality

    collaborator UNKNOWN
  • Zealand University Hospital

    lead OTHER

Principal Investigators

  • Maurice Antoine Lembeck, MD · Region Zealand, Nykøbing Falster Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2014-12-31
Completion
2015-01-31

Countries

  • Denmark

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 NCT02318680 on ClinicalTrials.gov