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Clinical Intervention in Frail Older People (FRAILCLINIC) (FRAILCLINIC)

Primary Purpose

Frailty Syndrome

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Intervention Geriatric Program
Sponsored by
Hospital Universitario Getafe
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Frailty Syndrome focused on measuring Frailty, Frailty tools, Clinical settings, Disability, Quality of life, Functional Autonomy

Eligibility Criteria

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

Inclusion Criteria:

  1. Frailty patients older than 75 years old attended in the settings of care.
  2. Willing and able to provide informed consent

Exclusion Criteria:

  1. Lack of capacity to give informed consent.
  2. Those unable or unwilling to cooperate with any of the assessments

Sites / Locations

  • Hopsital Universitario de Getafe

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention Geriatric Program

Usual clinical practice

Arm Description

A comprehensive management plan of the frail patients, covering both in-hospital and postdischarge time, according to the treating physicians (s) surgeon and the performance of a geriatrician . This management will consist of the therapeutic plan, access to geriatric levels of care, coordination with primary and social care, rehabilitation, and discharge plan.

A comprehensive management plan of the frail patients, covering both in-hospital and postdischarge time, agreed with the treating physicians (s) surgeon.

Outcomes

Primary Outcome Measures

Functional Status assessed using the Barthel index for Basic Activities of Daily Living
will be assessed using the Barthel index for Basic Activities of Daily Living
Functional Status assessed using the Lawton index for Instrumental Activities of Daily Living
will be assessed using the Lawton index for Instrumental Activities of Daily Living
Institutionalization (defined as the number of patients newly addressed to nursing)
defined as the number of patients newly addressed to nursing
Mortality
number of deaths occurred either during hospitalization or at follow-up

Secondary Outcome Measures

Full Information

First Posted
March 26, 2015
Last Updated
September 8, 2023
Sponsor
Hospital Universitario Getafe
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1. Study Identification

Unique Protocol Identification Number
NCT02643069
Brief Title
Clinical Intervention in Frail Older People (FRAILCLINIC)
Acronym
FRAILCLINIC
Official Title
Feasibility and Effectiveness of Frailty Screening and Management Programs Implemented in Different Clinical Settings (FRAILCLINIC)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
February 2014 (Actual)
Primary Completion Date
March 2021 (Actual)
Study Completion Date
March 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Universitario Getafe

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Frailty is the main risk factor for the development of incident disability in older people and one of the most important for other adverse outcomes (death, hospitalisation, falls, and permanent institutionalisation). Although frailty is a frequent condition in older adults who attend hospitals, little is known about its true prevalence in different settings of care. Better knowledge of this issue will inform the rational design of more effective strategies aimed at providing fitted care for these patients. Thus, the current study will potentially have impact on the quality of care for frail patients by revealing the prevalence of frailty in different settings of care, the difficulties in detection and management of frailty in these settings and the best instruments to detect frailty. The investigators proposal brings together 6 partners in the European Union (EU) from three countries, with the common aim of studying the feasibility of a program to detect frail older patients in high risk clinical settings.
Detailed Description
Quality assurance plan: To perform regular monitoring according to the International Conference on Harmonisation (ICH) and Good Clinical Practice (GCP): The data will be evaluated according to the protocol and source documents. To give training to the centres involved in the study. To check the electronic Case Report Form (eCRF) Data checks to compare data entered into the registry: The eCRF has been designed to capture all data required in the protocol. A unique eCRF will be completed for subject, taking into account the protection law in each country of the study.Subjects will be identified by a unique subject number (with key held by the relevant partner), so none id card number will not be recorded on the eCRF or the database. The monitor will guarantee that the eCRF is fully and correctly fill up according to the source documents. The researcher will assure that all data recorded in the eCRF coincide with the information recorded in the source documents. Plan for missing data to address situations where variables are reported as missing: The investigators will check the missing data in each eCRF and source documents. Statistical analysis: Data will be analyzed using STATA®. Descriptive statistics will be reported and histograms will assess the distribution of frailty scores in each scale. Each analysis will be categorised according to frail, prefrail or robust patients.The prevalence of frailty will be calculated for each scale based on the score thresholds and relationships between frailty and age and other variables will be evaluated. Agreement among scales will be examined using the Cohen kappa statistic. Receiver operator characteristic (ROC) curves will be constructed to compare the area under the ROC curve (AUC) for each scale for available outcomes. Sample Size: A minimum of 50 patients will be studied in each clinical setting, providing a database of 900 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Frailty Syndrome
Keywords
Frailty, Frailty tools, Clinical settings, Disability, Quality of life, Functional Autonomy

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
821 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention Geriatric Program
Arm Type
Experimental
Arm Description
A comprehensive management plan of the frail patients, covering both in-hospital and postdischarge time, according to the treating physicians (s) surgeon and the performance of a geriatrician . This management will consist of the therapeutic plan, access to geriatric levels of care, coordination with primary and social care, rehabilitation, and discharge plan.
Arm Title
Usual clinical practice
Arm Type
No Intervention
Arm Description
A comprehensive management plan of the frail patients, covering both in-hospital and postdischarge time, agreed with the treating physicians (s) surgeon.
Intervention Type
Other
Intervention Name(s)
Intervention Geriatric Program
Intervention Description
The investigators will implemented programs to detected and manage care for older patients in four settings: Emergency room, oncology department, surgery departments making major surgery and Cardiology. The core intervention will consist of the following elements: comprehensive geriatric assessment, coordination with primary ans social care, integrated and continued care, access to rehabilitation facilities, management of drug treatment avoiding polypharmacy and stressing adherence.
Primary Outcome Measure Information:
Title
Functional Status assessed using the Barthel index for Basic Activities of Daily Living
Description
will be assessed using the Barthel index for Basic Activities of Daily Living
Time Frame
36 months
Title
Functional Status assessed using the Lawton index for Instrumental Activities of Daily Living
Description
will be assessed using the Lawton index for Instrumental Activities of Daily Living
Time Frame
36 months
Title
Institutionalization (defined as the number of patients newly addressed to nursing)
Description
defined as the number of patients newly addressed to nursing
Time Frame
36 months
Title
Mortality
Description
number of deaths occurred either during hospitalization or at follow-up
Time Frame
36 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Frailty patients older than 75 years old attended in the settings of care. Willing and able to provide informed consent Exclusion Criteria: Lack of capacity to give informed consent. Those unable or unwilling to cooperate with any of the assessments
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leocadio Rodriguez Mañas, IP
Organizational Affiliation
Hospital Universitario de Getafe
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hopsital Universitario de Getafe
City
Getafe
State/Province
Madrid
ZIP/Postal Code
28905
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
25468154
Citation
Rodriguez-Manas L, Fried LP. Frailty in the clinical scenario. Lancet. 2015 Feb 14;385(9968):e7-e9. doi: 10.1016/S0140-6736(14)61595-6. Epub 2014 Nov 6. No abstract available.
Results Reference
background
PubMed Identifier
16129869
Citation
Rockwood K, Song X, MacKnight C, Bergman H, Hogan DB, McDowell I, Mitnitski A. A global clinical measure of fitness and frailty in elderly people. CMAJ. 2005 Aug 30;173(5):489-95. doi: 10.1503/cmaj.050051.
Results Reference
background
PubMed Identifier
11253156
Citation
Fried LP, Tangen CM, Walston J, Newman AB, Hirsch C, Gottdiener J, Seeman T, Tracy R, Kop WJ, Burke G, McBurnie MA; Cardiovascular Health Study Collaborative Research Group. Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci. 2001 Mar;56(3):M146-56. doi: 10.1093/gerona/56.3.m146.
Results Reference
result
PubMed Identifier
24559204
Citation
Pena FG, Theou O, Wallace L, Brothers TD, Gill TM, Gahbauer EA, Kirkland S, Mitnitski A, Rockwood K. Comparison of alternate scoring of variables on the performance of the frailty index. BMC Geriatr. 2014 Feb 24;14:25. doi: 10.1186/1471-2318-14-25.
Results Reference
result
PubMed Identifier
24597624
Citation
Drubbel I, Numans ME, Kranenburg G, Bleijenberg N, de Wit NJ, Schuurmans MJ. Screening for frailty in primary care: a systematic review of the psychometric properties of the frailty index in community-dwelling older people. BMC Geriatr. 2014 Mar 6;14:27. doi: 10.1186/1471-2318-14-27.
Results Reference
result
PubMed Identifier
24028357
Citation
Theou O, Brothers TD, Mitnitski A, Rockwood K. Operationalization of frailty using eight commonly used scales and comparison of their ability to predict all-cause mortality. J Am Geriatr Soc. 2013 Sep;61(9):1537-51. doi: 10.1111/jgs.12420. Epub 2013 Aug 26.
Results Reference
result
PubMed Identifier
22836700
Citation
Morley JE, Malmstrom TK, Miller DK. A simple frailty questionnaire (FRAIL) predicts outcomes in middle aged African Americans. J Nutr Health Aging. 2012 Jul;16(7):601-8. doi: 10.1007/s12603-012-0084-2.
Results Reference
result

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Clinical Intervention in Frail Older People (FRAILCLINIC)

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