- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02303249
Interventional Study of Videoconferences Between Hospital and Municipality - a Randomized Controlled Trial (Tele-hjem)
Interventional Study of Videoconferences Between Hospital and Municipality After Discharge From Roskilde and Køge Hospitals - a Randomized Controlled Trial
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study consists of two parts: First, the project nurse reviews the patients discharge together with the nurse from the hospital ward. Next, the patient is discharged from the hospital and meets the nurse from the municipality at home. Together with the patient the nurse form the municipality reviews:
- Documents from the hospital
- Medicine
- Nutrition
- Mobility
- Assessment of the need for health care services from the municipality
All patients in the project - both patients in the intervention group and patients in the control group - will receive treatment and care equivalent to normally applicable quality standards.
In 2011 4387 patients were discharged Monday to Friday from the Medical and Geriatric Departments at Roskilde and Køge Hospital to one of the seven municipalities. Of these, 1204 persons (27%) were readmitted (in any department) within 180 days. It is expected that the study demonstrates a reduction of ≥ 6 percentage points (from 27% to 21%) with a power of 80% and a significance level of 5%. There will be a need for 792 patients in both control and intervention group, ie 1584 in total.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Køge, Denmark
- Region Zealand, Roskilde and Køge Hospitals
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
Review of discharges and cross-sectoral video conferencing immediately after discharge
|
The intervention is video conference which is randomized and is an intervention that is assigned by the investigator.
|
|
No Intervention: Control
Standard health care services
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The proportion of patients who are readmitted
Time Frame: 180 days
|
Acute readmissions to any hospital in Denmark
|
180 days
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Use of municipal services (nursing, practical help, personal care)
Time Frame: 4 months
|
4 months
|
|
Time to readmission
Time Frame: 180 days
|
180 days
|
|
Total number of readmissions
Time Frame: 180 days
|
180 days
|
|
Total number of days of readmission
Time Frame: 180 days
|
180 days
|
|
The number of contacts with general practitioner
Time Frame: 180 days
|
180 days
|
|
Death
Time Frame: 180 days
|
180 days
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Solvejg Henneberg Pedersen, dr., Region Zealand
- Principal Investigator: Birgitte Dreyer Sørensen, cand. scient. san. publ., Region Zealand
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- SJ-337
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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