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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02422849
Other study ID # SHS-ED-01-2013
Secondary ID
Status Completed
Phase N/A
First received March 27, 2015
Last updated February 13, 2016
Start date November 2013
Est. completion date June 2015

Study information

Verified date February 2016
Source University of Southern Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

the elderly population (+ 65 years) is increasing. Acute medical conditions often leads to hospital admissions in this age group. However hospital admission is linked to adverse events. like confusion, medication errors or new infections.

the ACCESS project aims to examine alternatives to acute admissions for senior medical patients.

the aims are:

1. How many patients will be admitted to hospital due to acute medical conditions if cared for by their own General Practitioner (GP) versus a hospital intern specialist ?

2. how many patients will be admitted to hospital due to acute medical conditions if cared for by acute team in their home versus in specialised care centres ?


Recruitment information / eligibility

Status Completed
Enrollment 131
Est. completion date June 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Both
Age group 60 Years and older
Eligibility Inclusion Criteria:

- acute medical condition requiring immediate intervention.

Exclusion Criteria:

- GP not available next days

- absolutely admission requiring condition

- no informed consent obtainable

- nursing home resident

- inclusion in ACCESS within the last 3 months

- home care capacity limit reached

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
hospital specialist

General Practitioner


Locations

Country Name City State
Denmark Aabenraa Sygehus Emergency Department Aabenraa

Sponsors (1)

Lead Sponsor Collaborator
University of Southern Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of participants with hospital admission 3 months after inclusion No
Secondary change from baseline in De Morton Mobility Index (DEMMI) 3 months after inclusion No
Secondary change from baseline in quality of life (EQ5D scale) 3 months after inclusion No
Secondary change from baseline in Orientation Memory-Concentration (OMC) 3 months after inclusion No
Secondary patient and relatives satisfaction questionnaire 3 months after inclusion No
See also
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