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Indonesia Frailty, Aging, and Longitudinal Study (INA-FRAGILE)

U

University of Indonesia (UI)

Status

Unknown

Conditions

Quality of Life
Frailty

Study type

Observational

Funder types

Other

Identifiers

NCT02345083
INA-FRAGILE01

Details and patient eligibility

About

Frailty is a dynamic process from fit (robust) and pre-frail elderly. There is no previous study that determine the risk factors from fit to pre-frailty and pre-frailty to frailty in Indonesian elderly.

This study was aimed to define the risk factors and clinical outcomes of frailty transitional status in Indonesian elderly.

Full description

Frailty is an age-associated, biological syndrome characterized by decreased biological reserves, due to dysregulation of several physiological systems, which puts an individual at risk when facing minor stressors, and is associated with poor outcomes (ie, disability, death, and hospitalization).

Frailty identifies a high-risk subgroup and offers characteristics of great clinical importance: a higher reversibility at early stages than disability, and a higher predictive value than chronic disease for adverse outcomes at older ages. It is also the most common condition leading to death in community-dwelling older people.

However, there is current consensus that physical frailty is potentially reversible. It is hence useful to objectively detect frailty among frail elderly persons, as frailty indices serve a useful purpose for risk stratification, predicting need for institutional care and planning of services needed.

To date, there is no study or information about frailty status in Indonesia elderly. This study was aimed to define the risk factors and clinical outcomes of frailty transitional status in Indonesian elderly.

Enrollment

300 estimated patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Elderly aged >= 60 years old
  2. Fit (robust) or pre-frailty;
  3. Capable to understand and carry-out the instruction.

Exclusion criteria

  1. Unwilling to join the study;
  2. Abbreviated Mental Test (AMT) score < 8;
  3. Geriatric Depression Scale (GDS) score >= 10;
  4. Body mass index (BMI) <18,5 Kg/m2;
  5. Malnutrition (according to Mini Nutritional Assessment/MNA);
  6. Liver cirrhosis, severe liver dysfunction, or serum ALT levels >3 times upper normal limit;
  7. Acute illness during inclusion period, eg. pneumonia, pain due to acute arthritis (visual analog scale >6/10), stroke attack, crisis hypertension;
  8. Severe cardiac dysfunction: acute decompensated heart failure and/or chronic heart failure functional class III or IV (New York Heart Association classification);
  9. Severe pulmonary dysfunction: acute exacerbation of chronic obstructive lung disease stage III or IV (GOLD classification), and/or PaO2 levels < 60 mmHg.

Trial contacts and locations

1

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Central trial contact

Siti Setiati, Prof, MD

Data sourced from clinicaltrials.gov

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