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Clinical Trials/NCT01916876
NCT01916876
Withdrawn
N/A

A Randomised Controlled Trial of an Integrated Post-discharge Transitional Care Package for General Medical In-patients in Cape Town, South Africa

University of Cape Town2 sites in 1 countryMarch 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Follow-up Study
Sponsor
University of Cape Town
Locations
2
Primary Endpoint
All cause mortality
Status
Withdrawn
Last Updated
11 years ago

Overview

Brief Summary

The post discharge time is a vulnerable time for general medical in-patients, with high rates of adverse events that may cause unnecessary readmissions and even death. A recent study of 415 patients discharged from the general medical wards at Groote Schuur Hospital, demonstrated a very high 12 month mortality of 35%. The majority of these deaths were classified as "unexpected". The reasons for this were not further examined, but it was speculated, given the authors' knowledge of the public sector in Cape Town, that three related factors contribute significantly to this early mortality: i) a lack of continuity of care, with patients not necessarily accessing the primary care support treatment that they need or being able to access early post discharge follow-up (for example for anti-retroviral or anti-tuberculous care); ii) the inability of primary care to deal with the complex nature of the discharged patients, most whom have significant co-morbid disease; iii) A lack of optimisation of therapy for chronic disease after acute discharge.

The investigators hypothesise that an integrated post-discharge transitional care package, which includes an early medical specialist follow-up in the first 3 months after hospital discharge will decrease the 6- and 12-month mortality and re-admission rate amongst general medical hospital admissions in Cape Town, South Africa. Our study will compare an integrated package, suitable to implementation if effective, with current standard discharge packages.

Registry
clinicaltrials.gov
Start Date
March 2015
End Date
May 2016
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jonathan Peter

Honorary Consultant, Department of Medicine

University of Cape Town

Eligibility Criteria

Inclusion Criteria

  • Patients referred for admission to general medical wards (including within hospital transfer e.g. ICU discharge)
  • \>18 years and willing to give informed consent

Exclusion Criteria

  • Patient admitted directly to intensive care unit
  • Patient refusing consent or \<18 years old
  • Patients electively admitted
  • Patients without phone numbers who cannot provide any telephone contact details for a co-habitant, relative or neighbour.

Outcomes

Primary Outcomes

All cause mortality

Time Frame: 12 months

All cause 12-month mortality will be evaluated at 12-months post enrolment. Data on mortality will be acquired through telephonic patient/family contact and review of provincial death registry

Secondary Outcomes

  • All cause mortality(6 months)
  • Hospital readmission rate(12 months)
  • Bartel index(12 months)
  • Karnofsky performance score(12 months)

Study Sites (2)

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