Establishment and application of an early predictive model of frailty for older inpatients based on nutritional risk screening

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100044148

Enrollment

Unknown

Registered

2021-03-11

Start date

2021-04-01

Completion date

Unknown

Last updated

2021-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nutritional risk and frailty among the aging population

Interventions

case series:Nil

Eligibility

Sex/Gender

All

Age

65 Years to 99 Years

Inclusion criteria

Inclusion criteria: Aged >= 65 years; Estimated survival time > 3 months; Length of Hospital stay >= 4 days; Barthel Index >= 61 points (ie basic self-care in daily life); existing nutritional risk, which is, the Chinese version of mini nutritional assessment short-form (MNA-SF) is 0-11 points; the patient (or family member) voluntarily participates and signs the informed consent form.

Exclusion criteria

Exclusion criteria: Admitted to the hospital due to anorexia nervosa, acute pancreatitis, acute liver failure, cystic fibrosis or stem cell transplantation; suffering from acute infectious diseases or chronic wasting diseases, such as tuberculosis, malignant tumors, HIV infection, etc.; suffering from heart, lung or People with any life-threatening serious diseases in other organs; severe chronic gastrointestinal diseases; patient suffering from schizophrenia, depression and other mental illnesses; patients with persistent disturbances in consciousness or communication, unable to communicate effectively and their caregivers are unable to provide effective information; Those who have participated in clinical trials within 3 months; patients who have participated in the modeling of the first phase of the study; patients hospitalized in the intensive care unit (ICU), cardiovascular care unit (CCU), Medical intensive care units (MICU), and respiratory intensive care unit (RICU).

Design outcomes

Primary

Measure	Time frame
adverse clinical outcome within 30 days;	—

Secondary

Measure	Time frame
length of hospital stay, LoS;Health-related quality of life, HRQoL;falls;Myokines;	—

Countries

China

Contacts

Public ContactXinjuan Wu

Chinese Academy of Medical Sciences - Peking Union Medical College, Peking Union Medical College Hospital

wuxinjuan@sina.com+86 18612671300

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 21, 2026