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SHIP-AGE: Frailty, Renal Function, and Multi-component Primary Care in Rural Mecklenburg-Western Pomerania (MV-FIT)

Primary Purpose

Frailty Syndrome

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Multi-factorial geriatric assessment, monitoring & management systems
Sponsored by
University Medicine Greifswald
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Frailty Syndrome focused on measuring Chronic kidney disease, Frailty, Falls, Cognitive decline, Multi-component interventions, Rural communities

Eligibility Criteria

65 Years - 100 Years (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: age 65 years or older mGFR > 30 mL/min per 1.73 m2 being able to understand and give written informed consent. Exclusion Criteria: bedridden palliative inability to consent severe dementia inability to speak lack of compliance (paracusis, inability to fulfill at least 60% of the assessments)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Multi-factorial geriatric assessment, monitoring & management systems

    Arm Description

    All participants in the observational/interventional study (MV-FIT) will receive guideline-based, multi-factorial geriatric assessment, monitoring & managements (multi-component healthcare). Other: GFR Measuremments, Blood sampling, Urine sampling

    Outcomes

    Primary Outcome Measures

    Frailty
    The primary outcome will be frailty from baseline to follow-up at 36 months post subject inclusion (i.e. Frail vs. non-Frail). The frailty phenotype defines frailty as a clinical syndrome meeting three or more of five phenotypic criteria: (1) unintentional body weight loss (2) slow walking pace, (3) self-reported exhaustion, (4) muscle weakness, and (5) self-reported low physical activity.
    body weight loss
    unintentional body weight loss (determined weight in kilograms); see phenotype criteria (# 1) above
    slow walking pace
    slow walking pace (determined by walking speed measurements in m/sec); see phenotype criteria (# 2) above
    exhaustion
    self-reported exhaustion (determined by questionnaire), see phenotype criteria (# 3) above
    muscle weakness
    muscle weakness (determined by handgrip and jump strengths in kg); see phenotype criteria (# 4) above
    low physical activity
    (5) self-reported low physical activity (determinded by questionnaire); see phenotype criteria (# 5) above

    Secondary Outcome Measures

    Frailty transition
    Frailty transition (pre-frailty, in which one or two criteria (see above) are present)
    mGFR transition
    mGFR transition (transition from GFR KDIGO (Kidney Disease: Improving Global Outcomes) Stage 2 CKD in mL/min per 1.73 m2 to KDIGO Stage 3 in mL/min per 1.73 m2)
    patient welfare
    self-reported patient welfare (questionnaire)
    ability to live independently
    self-reported ability to live independently (Barthel Index for Activities of Daily Living (ADL))
    cognitive decline
    cognitive decline
    number of falls
    self-reported number of falls
    admission to hospitals
    self-reported admission to hospitals
    referrals to nursing homes
    self-reported referrals to nursing homes
    mortality
    all-cause mortality in primary care

    Full Information

    First Posted
    June 13, 2023
    Last Updated
    July 18, 2023
    Sponsor
    University Medicine Greifswald
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05962203
    Brief Title
    SHIP-AGE: Frailty, Renal Function, and Multi-component Primary Care in Rural Mecklenburg-Western Pomerania
    Acronym
    MV-FIT
    Official Title
    SHIP-AGE: Frailty, Renal Function, and Multi-component Primary Care in Rural Mecklenburg-Western Pomerania.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2023 (Anticipated)
    Primary Completion Date
    June 30, 2028 (Anticipated)
    Study Completion Date
    December 31, 2029 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University Medicine Greifswald

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Chronic kidney disease (CKD) is a leading risk factor for cardiovascular and all-cause mortality among the elderly. Mecklenburg-Western Pomerania has the largest prevalence of CKD in Germany and Europe. The CKD impact in primary care strategies to reduce frailty syndrome in the elderly is unknown. For this purpose, about 820 elderly participants will be included in an observational study (MV-FIT), who will undergo an multi-factorial geriatric assessment, monitoring & management program, specifically designed to avoid frailty. The goal of the full-scale study is to evaluate the impact of CKD in multi-component primary care strategies to reduce frailty among elderly persons in rural Mecklenburg-Western Pomerania. MV-FIT will be conducted on individuals in rural Mecklenburg-Western Pomerania, who will be observed over a period of 3 years. The Study of Health in Pomerania (SHIP) is a population-based epidemiological, two independent-cohort, study (SHIP and SHIP-TREND). SHIP cohorts have been followed for >24 years. SHIP/SHIP TEND participants >60 years or older will studied by a follow-up survey. The aim is to gain new insights into the development of frailty and to develop strategies for keeping those affected healthy.
    Detailed Description
    Our study is a longitudinal population-based epidemiological SHIP-cohort study combined with a prospective, multi-centered, observational/interventional investigation. MV-FIT is an observational study of individuals aged 65 years or older with mGFR >30 mL/min (n=~820). All participants in the observational/interventional study will receive guideline-based, multi-factorial geriatric assessment, monitoring & managements (multi-component healthcare). Subjects will be stratified by mGFR. Objectives are 1) to implement multi-component healthcare specifically comprised of components to reduce frailty and incident falls, 2) to improve compliance and adherence to the multi-component healthcare for frailty and improvement of patient welfare, ability to live independently, quality-of-life, number of falls, referrals to nursing homes, all-cause mortality in primary care of the elderly, 3) to seek the elderly individuals' experience during the course of multi-factorial primary care intervention through In-depth interviews, 4) to clarify the burden of CKD on frailty and health status, and 5) to identify novel risk factors and mechanisms for frailty and pre-frailty. MV-FIT data will be corroborated by SHIP/SHIP-TREND data.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Frailty Syndrome
    Keywords
    Chronic kidney disease, Frailty, Falls, Cognitive decline, Multi-component interventions, Rural communities

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Model Description
    Multivariable logistic regression; Multivariable Cox regression, Chi-Square-Test, Propensity score matching
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    820 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Multi-factorial geriatric assessment, monitoring & management systems
    Arm Type
    Experimental
    Arm Description
    All participants in the observational/interventional study (MV-FIT) will receive guideline-based, multi-factorial geriatric assessment, monitoring & managements (multi-component healthcare). Other: GFR Measuremments, Blood sampling, Urine sampling
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    Multi-factorial geriatric assessment, monitoring & management systems
    Other Intervention Name(s)
    Community-based and home-based exercise programs
    Intervention Description
    Multi-factorial geriatric assessment, monitoring & management systems, e.g. community-based and home-based exercise programs, polypharmacy
    Primary Outcome Measure Information:
    Title
    Frailty
    Description
    The primary outcome will be frailty from baseline to follow-up at 36 months post subject inclusion (i.e. Frail vs. non-Frail). The frailty phenotype defines frailty as a clinical syndrome meeting three or more of five phenotypic criteria: (1) unintentional body weight loss (2) slow walking pace, (3) self-reported exhaustion, (4) muscle weakness, and (5) self-reported low physical activity.
    Time Frame
    from baseline to follow-up at 36 month
    Title
    body weight loss
    Description
    unintentional body weight loss (determined weight in kilograms); see phenotype criteria (# 1) above
    Time Frame
    36 months
    Title
    slow walking pace
    Description
    slow walking pace (determined by walking speed measurements in m/sec); see phenotype criteria (# 2) above
    Time Frame
    36 months
    Title
    exhaustion
    Description
    self-reported exhaustion (determined by questionnaire), see phenotype criteria (# 3) above
    Time Frame
    36 months
    Title
    muscle weakness
    Description
    muscle weakness (determined by handgrip and jump strengths in kg); see phenotype criteria (# 4) above
    Time Frame
    36 months
    Title
    low physical activity
    Description
    (5) self-reported low physical activity (determinded by questionnaire); see phenotype criteria (# 5) above
    Time Frame
    36 months
    Secondary Outcome Measure Information:
    Title
    Frailty transition
    Description
    Frailty transition (pre-frailty, in which one or two criteria (see above) are present)
    Time Frame
    36 months
    Title
    mGFR transition
    Description
    mGFR transition (transition from GFR KDIGO (Kidney Disease: Improving Global Outcomes) Stage 2 CKD in mL/min per 1.73 m2 to KDIGO Stage 3 in mL/min per 1.73 m2)
    Time Frame
    36 months
    Title
    patient welfare
    Description
    self-reported patient welfare (questionnaire)
    Time Frame
    36 months
    Title
    ability to live independently
    Description
    self-reported ability to live independently (Barthel Index for Activities of Daily Living (ADL))
    Time Frame
    36 months
    Title
    cognitive decline
    Description
    cognitive decline
    Time Frame
    36 months
    Title
    number of falls
    Description
    self-reported number of falls
    Time Frame
    36 months
    Title
    admission to hospitals
    Description
    self-reported admission to hospitals
    Time Frame
    36 months
    Title
    referrals to nursing homes
    Description
    self-reported referrals to nursing homes
    Time Frame
    36 months
    Title
    mortality
    Description
    all-cause mortality in primary care
    Time Frame
    36 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    65 Years
    Maximum Age & Unit of Time
    100 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: age 65 years or older mGFR > 30 mL/min per 1.73 m2 being able to understand and give written informed consent. Exclusion Criteria: bedridden palliative inability to consent severe dementia inability to speak lack of compliance (paracusis, inability to fulfill at least 60% of the assessments)
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Maik Gollasch, MD, PhD
    Phone
    +493836257594
    Email
    maik.gollasch@med.uni-greifswald.de
    First Name & Middle Initial & Last Name or Official Title & Degree
    Julia Rüdebusch, PhD
    Phone
    +49 (0) 3834-86-7423
    Email
    julia.ruedebusch@uni-greifswald.de
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Maik Gollasch, MD, PhD
    Organizational Affiliation
    University Medicine Greifswald
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    SHIP-AGE: Frailty, Renal Function, and Multi-component Primary Care in Rural Mecklenburg-Western Pomerania

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