NCT02303249

Brief Summary

The study aims to assess whether the review of discharge planning followed by a cross-sectoral video conference in connection with discharge of medical and geriatric patients at Roskilde and Køge hospitals as well as patients from the Emergency Department at Køge Hospital reduces the proportion of patients who are readmitted within 180 days. Project nurses at the two hospitals identifies all patients fulfilling the inclusion criteria (above 55 years of age, discharged to their own home), get informed consent and performs the video conferences. Within a few hours after discharge a video conference is held in the patient´s home including the patient,the municipal nurse and the project nurse at the hospital. During the video conference the discharge is reviewed using a structured assessment. The survey is conducted as an open, randomized intervention study.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
1,387

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jul 2013

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2013

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

November 7, 2014

Completed
20 days until next milestone

First Posted

Study publicly available on registry

November 27, 2014

Completed
4 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2014

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2015

Completed
Last Updated

January 12, 2015

Status Verified

January 1, 2015

Enrollment Period

1.4 years

First QC Date

November 7, 2014

Last Update Submit

January 9, 2015

Conditions

Outcome Measures

Primary Outcomes (1)

  • The proportion of patients who are readmitted

    Acute readmissions to any hospital in Denmark

    180 days

Secondary Outcomes (6)

  • Use of municipal services (nursing, practical help, personal care)

    4 months

  • Time to readmission

    180 days

  • Total number of readmissions

    180 days

  • Total number of days of readmission

    180 days

  • The number of contacts with general practitioner

    180 days

  • +1 more secondary outcomes

Study Arms (2)

Intervention

EXPERIMENTAL

Review of discharges and cross-sectoral video conferencing immediately after discharge

Other: Review of discharges and cross-sectoral video conferencing immediately after discharge

Control

NO INTERVENTION

Standard health care services

Interventions

The intervention is video conference which is randomized and is an intervention that is assigned by the investigator.

Intervention

Eligibility Criteria

Age55 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Discharge from the Medical Department and Geriatric Department at Roskilde and Køge hospitals or the Emergency Department at Køge Hospital.
  • Address in Køge, Greve, Faxe, Solrød, Lejre, Stevns or Roskilde municipalities. Discharges between 8 am and 4 pm Monday-Friday. Acute/subacute admission to the hospital

You may not qualify if:

  • Patients who cannot give consent to participation. Discharge to a nursing home or relief care home. Patients with planned readmission. Former participant in the study. Patients who are included in the Sub Acute Project. Patients who needs terminal care

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Region Zealand, Roskilde and Køge Hospitals

Køge, Denmark

Location

Study Officials

  • Solvejg Henneberg Pedersen, dr.

    Region Zealand

    STUDY DIRECTOR
  • Birgitte Dreyer Sørensen, cand. scient. san. publ.

    Region Zealand

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 7, 2014

First Posted

November 27, 2014

Study Start

July 1, 2013

Primary Completion

December 1, 2014

Study Completion

January 1, 2015

Last Updated

January 12, 2015

Record last verified: 2015-01

Locations