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Ambulatory Geriatric Evaluation - Frailty Intervention Trial (AGE-FIT)

Primary Purpose

Frail Elderly, Deaths

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
The intervention group
control group
Sponsored by
Linkoeping University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Frail Elderly focused on measuring quality of life, feeling of security, costs, multiprofessional team, geriatric competence

Eligibility Criteria

75 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Elderly 75 years and above
  • Have been hospitalized three or more times in the last 12 months
  • Have three or more diagnoses in their medical records according to the International Classification of Diseases (ICD-10)
  • Live in their own homes (not nursing home) in the municipality of Norrkoeping
  • Accept to participate in the study.

Exclusion criteria:

- Fulfilling the inclusion criteria but living in a special accommodation for the elderly

Sites / Locations

  • Department of Geriatric Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

The intervention group

Control group

Arm Description

The intervention group will receive Comprehensive Geriatric Assessment and follow up as a complement to the same standard health care services as the control group. The Comprehensive Geriatric Assessment and follow up will be provides through an outpatient facility that tailors care from a holistic perspective and, based on each patient's individual needs in line with the policy program that Sweden's pensioners' organizations have presented in 2010 together with the Swedish Association of Geriatric Medicine. The team includes, among other things. a. geriatricians, nurses, physiotherapists, assistance officer, dietician, pharmacist and co-operation with the dental hygienist.

The control group will receive care in the same way as usual meaning access to primary care, hospital in- and outpatient care and care received by the municipality. The only difference between the two groups are that the control group will not have access to the geriatric care team.

Outcomes

Primary Outcome Measures

Hospitalisation
Number of hospitalisations and in-care stays during the trial
Frailty
Unintentional weight loss ≥5% of the previous year. Exhaustion is assessed by two questions from the Centre for Epidemiologic Studies-Depression Scale. Low physical activity includes assessment of habitual physical activity level by using the Swedish version of the International Physical Activity Questionnaire short version (IPAQ-S).Slow walking speed is determined from the better of two attempts at usual "comfortable" walking speed over 4 m with or without a walking aid. Weakness (muscle strength) is assessed by maximal grip strength.

Secondary Outcome Measures

Cognition
Cognition is assessed by the Mini-Mental State Examination
Symptoms
Symptoms experienced during the previous week (frequency, intensity, and distress) are assessed by the "The Memorial Symptom Assessment Scale" (MSAS), which measures 32 different symptoms.
Depression
Depression is assessed using the Geriatric Depression Scale (GDS-15
Health related quality of life
Health related quality of life (HRQL) is assessed by using the Nottingham Health Profile, first part (NHP) and the generic "EuroQol" questionnaire (EQ-5D)
Nutrition
The Mini Nutritional Assessment form (MNA), is used to assess nutritional status. The MNA includes 18 items.
Activities of Daily Living
Barthels index
Falls
the patient is asked about falls in the last 6 months
Costs
1) Contact and extent of contact with the municipality measured by working hours 2) Number of: visits to day-care centres, in-hospital stays (type of clinic and extent of these), visits to primary care facilities, geriatric ambulatories or other specialist ambulatories 3) Admissions to nursing care facilities
Feeling of security of the patient
Questionnaire
Feeling of security of the relatives
Questionnaire
Quality of life of relatives
Questionnaire

Full Information

First Posted
September 19, 2011
Last Updated
March 29, 2014
Sponsor
Linkoeping University
Collaborators
Swedish Association of Local Authorities and Regions
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1. Study Identification

Unique Protocol Identification Number
NCT01446757
Brief Title
Ambulatory Geriatric Evaluation - Frailty Intervention Trial
Acronym
AGE-FIT
Official Title
Effectiveness of a Comprehensive CGA on Frailty in Community-dwelling Elderly People - A Randomised, Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
March 2011 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Linkoeping University
Collaborators
Swedish Association of Local Authorities and Regions

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The main purpose of this randomised controlled trial is to study if a Comprehensive Geriatric Assessment (CGA) and follow up for community-dwelling elderly people can improve outcomes such as health and health-related quality of life among both patients and relatives, feeling of safety among both patients and relatives and reduce costs, compared with usual care.
Detailed Description
Frail older adults are at increased risk of vulnerability and serious health problems. This leads to increased suffering and higher healthcare utilization. There are major gaps in the knowledge needed to create the most favourable care model for preventing frailty and increasing health-related of life. The purpose of this randomised controlled trial is to study if a Comprehensive Geriatric Assessment and follow up in community-dwelling elderly people can prevent frailty, hospitalisation and adverse effects of frailty, improve health and health-related quality of life, and reduce costs, compared with usual care. In a randomized, controlled trial with 24 months of follow-up, a total of 430 older adults with multimorbidity will be randomized into two groups. The intervention group will receive Comprehensive Geriatric Assessment and follow up and the same standard health care services as the control group. The Comprehensive Geriatric Assessment and follow up will be provides through an outpatient facility that tailors care from a holistic perspective and, based on each patient's individual needs in line with the policy program that Sweden's pensioners' organizations have presented in 2010 together with the Swedish Association of Geriatric Medicine. The team includes, among other things. a. geriatricians, nurses, physiotherapists, assistance officer, dietician, pharmacist and co-operation with the dental hygienist. The primary outcome is development of frailty and hospitalization. Secondary outcomes are adverse effects of frailty, health and health-related quality of life and costs. There is a knowledge gap of how health care can identify persons with frailty and risks for frailty and how to meet their specific care needs. The study aims to fill a clinically important knowledge gap that can guide further development of future care for older people with multi-morbidity and frailty. CGA is readily transferable to clinical practice.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Frail Elderly, Deaths
Keywords
quality of life, feeling of security, costs, multiprofessional team, geriatric competence

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
383 (Actual)

8. Arms, Groups, and Interventions

Arm Title
The intervention group
Arm Type
Experimental
Arm Description
The intervention group will receive Comprehensive Geriatric Assessment and follow up as a complement to the same standard health care services as the control group. The Comprehensive Geriatric Assessment and follow up will be provides through an outpatient facility that tailors care from a holistic perspective and, based on each patient's individual needs in line with the policy program that Sweden's pensioners' organizations have presented in 2010 together with the Swedish Association of Geriatric Medicine. The team includes, among other things. a. geriatricians, nurses, physiotherapists, assistance officer, dietician, pharmacist and co-operation with the dental hygienist.
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
The control group will receive care in the same way as usual meaning access to primary care, hospital in- and outpatient care and care received by the municipality. The only difference between the two groups are that the control group will not have access to the geriatric care team.
Intervention Type
Procedure
Intervention Name(s)
The intervention group
Other Intervention Name(s)
Geriatric care team
Intervention Description
Medical assessment (co-morbid condition, physical and neurological examination, medication review, nutrition, and blood-tests to identify anaemia, diabetes, metabolism and liver- and kidney function); assessment of functioning (ADL/IADL, fall risk), psychological assessment (cognitive decline and depression) and assessment of social and environmental conditions. The care plan is based on the CGA and will be individualised and carried out in discussion with the patient and his/her caregivers. The care will be carried out by an inter-professional Geriatric Team with employees from both the county council and the municipality. The team consists of a core team (including geriatrician and nurse) and a support team (including a social worker, occupational therapist, dietician, pharmacist, physiotherapist, and dental hygienist). The care will involve treatment for unstable medical conditions and support of patients and their caregivers. The team will have regular team conferences.
Intervention Type
Procedure
Intervention Name(s)
control group
Intervention Description
No intervention
Primary Outcome Measure Information:
Title
Hospitalisation
Description
Number of hospitalisations and in-care stays during the trial
Time Frame
24 months
Title
Frailty
Description
Unintentional weight loss ≥5% of the previous year. Exhaustion is assessed by two questions from the Centre for Epidemiologic Studies-Depression Scale. Low physical activity includes assessment of habitual physical activity level by using the Swedish version of the International Physical Activity Questionnaire short version (IPAQ-S).Slow walking speed is determined from the better of two attempts at usual "comfortable" walking speed over 4 m with or without a walking aid. Weakness (muscle strength) is assessed by maximal grip strength.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Cognition
Description
Cognition is assessed by the Mini-Mental State Examination
Time Frame
0 and 24 months
Title
Symptoms
Description
Symptoms experienced during the previous week (frequency, intensity, and distress) are assessed by the "The Memorial Symptom Assessment Scale" (MSAS), which measures 32 different symptoms.
Time Frame
0 and 24 months
Title
Depression
Description
Depression is assessed using the Geriatric Depression Scale (GDS-15
Time Frame
0 and 24 months
Title
Health related quality of life
Description
Health related quality of life (HRQL) is assessed by using the Nottingham Health Profile, first part (NHP) and the generic "EuroQol" questionnaire (EQ-5D)
Time Frame
0 and 24 months
Title
Nutrition
Description
The Mini Nutritional Assessment form (MNA), is used to assess nutritional status. The MNA includes 18 items.
Time Frame
0 and 24 months
Title
Activities of Daily Living
Description
Barthels index
Time Frame
0 and 24 months
Title
Falls
Description
the patient is asked about falls in the last 6 months
Time Frame
0 and 24 months
Title
Costs
Description
1) Contact and extent of contact with the municipality measured by working hours 2) Number of: visits to day-care centres, in-hospital stays (type of clinic and extent of these), visits to primary care facilities, geriatric ambulatories or other specialist ambulatories 3) Admissions to nursing care facilities
Time Frame
24 months
Title
Feeling of security of the patient
Description
Questionnaire
Time Frame
0, 12 and 24 months
Title
Feeling of security of the relatives
Description
Questionnaire
Time Frame
0, 12 and 24 months
Title
Quality of life of relatives
Description
Questionnaire
Time Frame
0, 12 and 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Elderly 75 years and above Have been hospitalized three or more times in the last 12 months Have three or more diagnoses in their medical records according to the International Classification of Diseases (ICD-10) Live in their own homes (not nursing home) in the municipality of Norrkoeping Accept to participate in the study. Exclusion criteria: - Fulfilling the inclusion criteria but living in a special accommodation for the elderly
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne W Ekdahl, Physisian
Organizational Affiliation
Linkopeing University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Geriatric Medicine
City
Norrkoeping
ZIP/Postal Code
60182
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
31277674
Citation
Klompstra L, Ekdahl AW, Krevers B, Milberg A, Eckerblad J. Factors related to health-related quality of life in older people with multimorbidity and high health care consumption over a two-year period. BMC Geriatr. 2019 Jul 5;19(1):187. doi: 10.1186/s12877-019-1194-z.
Results Reference
derived
PubMed Identifier
29386007
Citation
Lundqvist M, Alwin J, Henriksson M, Husberg M, Carlsson P, Ekdahl AW. Cost-effectiveness of comprehensive geriatric assessment at an ambulatory geriatric unit based on the AGe-FIT trial. BMC Geriatr. 2018 Jan 31;18(1):32. doi: 10.1186/s12877-017-0703-1.
Results Reference
derived
PubMed Identifier
25703450
Citation
Ekdahl AW, Wirehn AB, Alwin J, Jaarsma T, Unosson M, Husberg M, Eckerblad J, Milberg A, Krevers B, Carlsson P. Costs and Effects of an Ambulatory Geriatric Unit (the AGe-FIT Study): A Randomized Controlled Trial. J Am Med Dir Assoc. 2015 Jun 1;16(6):497-503. doi: 10.1016/j.jamda.2015.01.074. Epub 2015 Feb 18.
Results Reference
derived

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Ambulatory Geriatric Evaluation - Frailty Intervention Trial

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