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CompletedNCT03365453FRASER-VDUpdated Dec 12, 2024

Frailty in Elderly Patients Receiving Surgical or Percutaneous Procedures for Valvular Disorders

An interventional study of frailty evaluation in Age Problem, Aortic Valve Disease and Mitral Valve Disease, sponsored by University Hospital of Ferrara. Completed at 1 site in Italy. Open to participants aged 70 Years and older. Per ClinicalTrials.gov, last updated 2024-12-12.

Sponsored by University Hospital of Ferrara · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
450
Allocation
Not applicable
Ages
70 Years and older
Sex
All
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Study summary

In Italy, life expectancy at birth has reached 80 years in men and 85 in women; in about 50 years, life expectancy at the age of 80 has increased by an extraordinary 61% and 55%, respectively, due to more effective therapies and lower mortality of many diseases. Yet, chronic diseases are nowadays more important, and often coexist as comorbidity or multimorbidity, depending on whether an index condition has been considered. These conditions increase the risk of death and reduce functional autonomy in the elderly and, therefore, should be carefully considered within comprehensive geriatric assessment. The epidemiology of valvular disease shows a clear trend in age-dependent, as the number of events and their incidence increases with age, and about half are concentrates over 75 years.

In addition, some observational studies in elderly patients have suggested an association between frailty and cardiovascular disease: fragility and cardiovascular disease share a common biological pathway, and cardiovascular diseases may accelerate the onset of frailty. The frailty syndrome was identified in 25% to 50% of patients with cardiovascular disease, according to the rating scale used and the population studied. Frail patients with cardiovascular disease, in particular those undergoing invasive procedures or suffering from coronary artery disease and aortic valve disease, have a much higher adverse events and complications, suggesting the need for a more accurate functional stratification and a more careful evaluation of the risk/benefit ratio of some invasive procedures.

Among the numerous tests proposed in the literature for the functional evaluation and objective measures of physical capability in elderly patient, the Short Physical Performance Battery (SPPB) and the evaluation of hand grip strength (grip strength) are those characterized by an improved prognostic ability and an easy administration.

The present study is performed to assess if SPPB and handgrip are helpful to better stratify the prognosis (all-causes death and hospital admission for all causes) in elderly patients admitted to hospital for cardiac causes.

Read the detailed description

This is a prospective study. This a single centre study involving the Maria Cecilia Hospital (Ravenna, Italy).

The study is expected to enroll at least 450 consecutive patients with ≥70 years, which are admitted for:

GROUP A: severe aortic stenosis undergoing surgical aortic valve replacement GROUP B: severe aortic stenosis undergoing transcatheter valve implantation GROUP C: severe mitral regurgitation undergoing surgical repair GROUP D: severe mitral regurgitation undergoing MITRACLIP repair

In all patients, the following functional assessments will be performed before surgical/percutaneous intervention:

handgrip test (see definition below). Short Portable Mental Status Questionnaire (SPMSQ, see definition below). Short Physical Performance Battery (SPPB, see definition below). Multidimensional Prognostic Index (MPI, see definition below). The aim of the study is to assess the relationship between frailty score and prognosis

HANDGRIP (HGT). The handgrip test measures the force of contraction of the flexor muscles of the fingers through the use of a dynamometer. From literature it is known as such index correlates with the eventual malnutrition of the subject, with its capacity of recovery and functional recovery post-surgery, as well as to be in relation with age. In each patient, three measurements will be carried out. Will be taken into consideration for the study the highest value. The measurement will be performed as indicated by current guidelines, with the patient seated, with the dominant hand and the elbow flexed 90°. All medical personnel involved in the study performed a specific course to learn the proper management and execution of screening with handgrip tes and has personal experience in its proper execution.

SHORT PHYSICAL PERFORMANCE BATTERY (SPPB). The scale SPPB is a short battery of tests created to evaluate the functionality of the lower limbs. This battery is made up of 3 different sections designed to assess a balance with 3 tests: the maintenance of the position with the feet together for 10 seconds then the semi-tandem and finally tandem again for 10 seconds. The score of this section varies from a minimum of 0 if the patient is unable to maintain position with your feet together for at least 10 seconds to a maximum of 4 if he can accomplish all three tests. The second section of the test is intended to evaluate the progress of 4 linear meters and depending on the time of the performance section of the score ranges from 0 if unable, at one point if the performance has a longer duration of 8.7 seconds, for a up to 4 if he can accomplish the task in less than 4.80 sec. The third section investigates the ability of the battery to run for 5 consecutive times, getting up from a chair without using the arms in this regard that must be crossed in front of chest. Also in this case, the score ranges from 0 incapable or if the performance has a duration greater than 60 seconds, to a maximum of 4 if such performance is carried out in less than 11.20 seconds. The scores range from 0 (worst performance) to 12 (best performance).

A score between 5 and 9 shows seniors still independent, but with reduced physical performance, which can therefore be regarded as fragile and high risk, deserving of special attention and specific interventions, acts to reduce the risk of adverse consequences. Data in the literature confirm that the SPPB correlates with the risk of developing disability in mobility, in proportion to the decrease of the SPPB score, regardless of age, sex and presence of certain chronic diseases. The SPPB score then emerges as a powerful predictor of disability and mortality in the elderly population.

MULTIDIMENSIONAL PROGNOSTIC INDEX (MPI)

The Multidimensional Prognostic Index (MPI) is a prognostic tool based on a standard Comprehensive Geriatric Assessment (CGA) that predicts short- and long-term mortality in elderly subjects. The MPI includes 63 items distributed in 8 domains of CGA as follows:

Activities of Daily Living (ADL): 6 items Instrumental Activities of Daily Living (IADL): 8 items Short Portable Mental Status Questionnaire (SPMSQ): 10 items Mini Nutritional Assessement (MNA): 18 items Exton-Smith Scale (ESS): 5 items Cumulative Index Rating Scale - Comorbidity Index (CIRS-CI): 14 items Number of drugs used: 1 item Co-habitation status: 1 item On the basis of MPI values, it is possible to calculate the short- and long-term mortality risk of the older subjects and to define the severity grade of mortality risk: low, moderate and severe. Several studies showed that the prognostic accuracy of the aggregated MPI was significantly greater than the prognostic accuracy of its individual components considered singularly. Thus the multidimensional approach can be successfully used in elderly patients for both clinical and administrative purposes.

02

Conditions studied

  • Age Problem
  • Aortic Valve Disease
  • Mitral Valve Disease

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03

In context

Aortic Valve Disease

234 studies on the registry are indexed under Aortic Valve Disease; 75 are open to participants now.

This study's enrollment of 450 is above the median of 107 across 119 interventional studies indexed under Aortic Valve Disease.

Browse Aortic Valve Disease studies →

Lead sponsor

University Hospital of Ferrara is the lead sponsor of 114 studies on the registry; 29 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
70 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • age ≥70
  • hospital admission for valvular disorders (severe aortic stenosis or severe mitral regurgitation) requiring surgical or percutaneous intervention

Exclusion criteria

Exclusion Criteria:

  • SPMSQ value ≤4
  • inability to stay upright
  • life expectancy \<3 months
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
450 participants (actual)

Study arms

  • Experimental
    frailty evaluation

    all consecutive patients admitted to hospital for valvular disorders more than 69 years will be evaluated with several frailty and comorbidities scores.

    Other: frailty evaluation

Interventions

  • Otherfrailty evaluation

    frailty and comorbidity scores

06

What researchers measure

Primary outcomes

  1. composite endpoint of all-cause mortality and all-cause hospital admission

    1-year cumulative incidence of all-cause mortality and all-cause hospital admission

    Time frame: 1-year

Secondary outcomes

  1. all-cause mortality

    1-year cumulative incidence of death for all-causes

    Time frame: 1-year

  2. cardiac death

    1-year cumulative incidence of cardiac death

    Time frame: 1-year

  3. cardiac adverse events

    1-year cumulative incidence of cardiac death, myocardial infarction, heart failure

    Time frame: 1-year

Other outcomes

  1. cerebrovascular accident

    1-year cumulative incidence of stroke and/or transient ischemic attack

    Time frame: 1-year

07

Study locations

1 site
  • Maria Cecilia Hospital
    Cotignola, Ravenna, Italy
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 12, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03365453
Collaborators
Maria Cecilia Hospital
Responsible party
Gianluca Campo (Associate Professor, University Hospital of Ferrara) — Principal investigator
First posted
Dec 7, 2017
Start date
Dec 1, 2017
Primary completion
Aug 31, 2022
Completion
Dec 7, 2024
Last update
Dec 12, 2024

Study contacts

Gianluca Campo
principal investigator · Azienda Ospedaliera Universitaria di Ferrara
Alberto Cremonesi
principal investigator · Maria Cecilia Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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