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Update on the Detection of Frailty in Older Adults

E

European University

Status

Enrolling

Conditions

Kinesiophobia
Quality of Life
Strength
Functionality
Depression
Functional Independence
Anxiety
Sarcopenia
Pain

Treatments

Diagnostic Test: Instrumental and Functional Tests that Assess Functional Capacity

Study type

Observational

Funder types

Other

Identifiers

NCT06218121
Detection of Frailty

Details and patient eligibility

About

The main objective is to update the diagnostic assessment of frailty by correlating several variables with the ultrasound image of the frail elderly patient.

Secondarily, the investigators intend to collect and analyze data on functional capacity and quality of life variables on the evolution of musculoskeletal symptoms, as well as on pain and psychological variables. Similarly, it is intended to make a record of different profiles and subtypes of frail older adult patients to be stored in Machine Learning in order to establish therapeutic intervention plans that allow both the evaluation and treatment of patients.

Full description

The present cohort study will be conducted in 500 older adults diagnosed with frailty.

The correlation of the demographic variables, physical functionality tests and psychoemotional constructs that will be analyzed in this study with the ultrasound image obtained from the patients will improve the ultrasound diagnosis of frailty, providing new information that will facilitate the work of healthcare personnel in the diagnosis and management of frailty.

Similarly, the use of Machine Learning will allow institutions to extract data on different patient profiles, signs and symptoms of frailty and the different risk factors that affect frailty patients, which will improve treatments and favor the development of educational programs tailored to the patient's needs.

Enrollment

500 estimated patients

Sex

All

Ages

62+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

A diagnosis of signs and symptoms of frailty by a geriatric physician in the research group will be used as the primary inclusion criterion. Frailty will be assessed and diagnosed using the frailty phenotype and the Clinical Frailty Scale.

Exclusion criteria

  • Acute myocardial infarction in the last 3 months and/or unstable angina pectoris
  • Uncontrolled arrhythmia, recent thromboembolism and terminal illness.
  • Patients undergoing MMII unloading or MMSS/MMII fractures in the last three months.
  • Patients with a functional gait index of 1 (Inability to walk)
  • Severe pain (7/10 VAS)
  • Previous neuromuscular pathology presenting with weakness
  • Medication that does not allow the patient's actual muscle reaction to be assessed
  • Severe cognitive impairment that would prevent collaboration and understanding of the tests to be performed.
  • Cardiovascularly unstable patients and uncontrolled arterial hypertension.

Trial design

500 participants in 1 patient group

Frail Older Adult Patients
Description:
For the cohort study, 500 frail older adult patients will be evaluated by means of instrumental and functional tests that assess their functional capacity, in addition to ultrasound imaging to study sarcopenia and nutrition, as well as psychological variables. The correlation between all functional, ultrasound, nutritional, and psychological variables will be analyzed. Through GLIM diagnosis, anthropometric data (weight, height, BMI) as well as analytical data including inflammation information (CRP and albumin) will be used to reach a diagnosis that allows comparison/correlation with the rest of the variable parameters. All available information will be collected during the follow-up in order to generate Machine Learning on the objective evolution and symptomatology of these patients, generating profiles that facilitate the most accurate and appropriate treatment for each patient.
Treatment:
Diagnostic Test: Instrumental and Functional Tests that Assess Functional Capacity

Trial contacts and locations

1

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Central trial contact

Eleuterio A. Sánchez Romero, PhD

Data sourced from clinicaltrials.gov

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