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Clinical Trials/NCT02790372
NCT02790372
Completed
N/A

The Effect of Comprehensive Geriatric Assessment and Case Conferencing on Neuropsychiatric Symptoms Among Patients in Norwegian Nursing Homes

Norwegian University of Science and Technology1 site in 1 country309 target enrollmentApril 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Dementia
Sponsor
Norwegian University of Science and Technology
Enrollment
309
Locations
1
Primary Endpoint
Prevalence of neuropsychiatric symptoms measured by neuropsychiatric inventory
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This study evaluates the effect of using comprehensive geriatric assessment in combination with case conferences on the prevalence of neuropsychiatric symptoms (also known as behavioral and psychological symptoms of dementia) in Norwegian nursing homes

Detailed Description

Long-term care patients in nursing homes (NH) are characterized by frailty and having multiple health problems and reduced quality of life. Some of these issues relates to the quality of care and do therefore possess a potential for improvement. There is a need for approaches enabling nurses to carry out effective interventions that can promote health related to sustain or improve the nursing home patients health status. Integrating a comprehensive geriatric assessment (CGA) and case conferencing (CC) might be an effective method to individualize care plans in order to improve quality of care. The intervention nursing homes will implement CGA, using the International resident instrument suite for Long Term Care Facilities (InterRai LTCF) and CC. The patients will be included and assessed three times during a 12-month period (control and intervention NHs). In the intervention NHs the results from the CGA will be reviewed in monthly CCs. The CCs are structured and consist of four main steps; evaluating the effects of earlier interventions, defining patients risks or area for improvement, defining the aetiology of the risk or problem, defining interventions and measures for improvement along with an appropriate method for evaluation. The CC group's consensus is basis for the patient's care plan.

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
April 5, 2017
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • registered as long term care patient
  • been in the nursing home for more than a month
  • Informed consent from the patient or legal guardians

Exclusion Criteria

  • life expectancy less than six months

Outcomes

Primary Outcomes

Prevalence of neuropsychiatric symptoms measured by neuropsychiatric inventory

Time Frame: 12 months

Measured by neuropsychiatric inventory

Secondary Outcomes

  • Depression measured by Cornell scale for depression in dementia(12 months)
  • Quality of life measured by the Quality of Life in Late-Stage Dementia Scale(12 months)
  • Activities in daily living measured by Physical self-maintenance scale(12 months)

Study Sites (1)

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