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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05962203
Other study ID # BB 161/22
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 1, 2023
Est. completion date December 31, 2029

Study information

Verified date July 2023
Source University Medicine Greifswald
Contact Maik Gollasch, MD, PhD
Phone +493836257594
Email maik.gollasch@med.uni-greifswald.de
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 820
Est. completion date December 31, 2029
Est. primary completion date June 30, 2028
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years to 100 Years
Eligibility 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)

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Multi-factorial geriatric assessment, monitoring & management systems
Multi-factorial geriatric assessment, monitoring & management systems, e.g. community-based and home-based exercise programs, polypharmacy

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Medicine Greifswald

Outcome

Type Measure Description Time frame Safety issue
Primary 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. from baseline to follow-up at 36 month
Primary body weight loss unintentional body weight loss (determined weight in kilograms); see phenotype criteria (# 1) above 36 months
Primary slow walking pace slow walking pace (determined by walking speed measurements in m/sec); see phenotype criteria (# 2) above 36 months
Primary exhaustion self-reported exhaustion (determined by questionnaire), see phenotype criteria (# 3) above 36 months
Primary muscle weakness muscle weakness (determined by handgrip and jump strengths in kg); see phenotype criteria (# 4) above 36 months
Primary low physical activity (5) self-reported low physical activity (determinded by questionnaire); see phenotype criteria (# 5) above 36 months
Secondary Frailty transition Frailty transition (pre-frailty, in which one or two criteria (see above) are present) 36 months
Secondary 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) 36 months
Secondary patient welfare self-reported patient welfare (questionnaire) 36 months
Secondary ability to live independently self-reported ability to live independently (Barthel Index for Activities of Daily Living (ADL)) 36 months
Secondary cognitive decline cognitive decline 36 months
Secondary number of falls self-reported number of falls 36 months
Secondary admission to hospitals self-reported admission to hospitals 36 months
Secondary referrals to nursing homes self-reported referrals to nursing homes 36 months
Secondary mortality all-cause mortality in primary care 36 months
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