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A Prospective Randomised Control Trial to Study the Effectiveness of a Health Service Innovation Using a Modified Virtual Ward Model to Prevent Unscheduled Readmission of High Risk Patients

A Prospective Randomised Control Trial to Study the Effectiveness of a Health Service Innovation Using a Modified Virtual Ward Model to Prevent Unscheduled Readmission of High Risk Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02325752
Enrollment
840
Registered
2014-12-25
Start date
2011-08-31
Completion date
2013-01-31
Last updated
2017-02-10

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

Conditions

Chronic Diseases

Keywords

readmission, chronic diseases

Brief summary

The investigators conducted an open randomized control study of patients who received the transitional care program versus patients who received usual care at the Singapore General Hospital from Aug 2011 to Sept 2012.

Detailed description

The investigators conducted an open randomized control study of patients who received the transitional care program versus patients who received usual care at the Singapore General Hospital from Aug 2011 to Sept 2012.

Interventions

OTHERIntervention

A multidisciplinary team delivered the transitional care program. Our transitional care program focused on four key areas: 1. Post discharge surveillance of the patient to ensure adherence to care plans. 2. Coordination of follow-up visits with specialist care providers. 3. Patent education and care giver training. 4. Activation of community and social services. Upon recruitment, the patients were interviewed and assessed by the team nurse prior to their discharge. Intervention starts upon discharge from the hospital. The duration of the intervention program was 3 months. A follow-up by telephone was made within 72 hours after discharge to assess patient's condition and adherence to treatment plan. Home visits were made within 2 weeks after discharge.

Sponsors

Agency for Integrated Care, Singapore
CollaboratorOTHER
Duke-NUS Graduate Medical School
CollaboratorOTHER
Singapore General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients with 2 or more unscheduled admission in the last 90 days to selected medical departments * LACE score of ≥10.

Exclusion criteria

* Non-residents * No telephone contact or a resident address * Residing in long term care facilities.

Design outcomes

Primary

MeasureTime frameDescription
Rate of readmission30 daysAny hospital admission after randomisation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026