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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02325752
Other study ID # 2011/380/E
Secondary ID
Status Completed
Phase N/A
First received December 21, 2014
Last updated February 9, 2017
Start date August 2011
Est. completion date January 2013

Study information

Verified date February 2017
Source Singapore General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 840
Est. completion date January 2013
Est. primary completion date October 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Intervention
A multidisciplinary team delivered the transitional care program. Our transitional care program focused on four key areas: Post discharge surveillance of the patient to ensure adherence to care plans. Coordination of follow-up visits with specialist care providers. Patent education and care giver training. 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.

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
Singapore General Hospital Agency for Integrated Care, Singapore, Duke-NUS Graduate Medical School

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of readmission Any hospital admission after randomisation 30 days
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