A Biopsychosocial Approach to Improving Multidimensional Frailty Status in Community-Dwelling Older Adults

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age60-80
SponsorHong Kong Baptist University

About this trial

Frailty is a common clinical syndrome that is becoming increasingly important as populations age worldwide. Individuals who are frail are at a higher risk for negative outcomes, such as falls, disability, hospitalizations, and even death. The understanding of frailty has evolved from a straightforward concept to a complex model that includes physical, psychological, cognitive, and social factors. Since frailty is not static and can change over time, early interventions can be beneficial. Nevertheless, research in this area has been challenging due to a lack of agreement on what frailty encompasses and an inadequate understanding of how its different components interact. Defining frailty as a multidimensional issue is essential to recognize the adverse effects that can arise from medical, psychological, and social influences. However, recent studies have not sufficiently addressed how these different aspects work together or developed effective multidimensional interventions.

Eligibility criteria

Qualifiers

Age 60 to 80

Willing and capable to participate in this study and training

Willing and capable to give informed consent to participate in this study

Preliminarily classified as physically prefrail/robust, in that they possess no more than three of the indicators on the Fried Frailty Index (FFI; unintentional weight loss, exhaustion, low physical activity, slow walking speed, weak grip strength; Bieniek et al., 2016)

Disqualifiers

History of systematic cardiovascular diseases causing stroke, Parkinson's disease, early stages of Alzheimer's disease, or cognitive impairment

Physical injuries or other conditions that would hinder regular attendance and participation in the assessments for the study

Concurrent major psychiatric disorder (e.g. major depressive disorder, schizophrenia) or drug and alcohol abuse

Unable to handle digital devices

Trial design

Treatments tested in this trial

  • Exercise
  • Psychosocial
  • Nutritional

Treatment groups

308 Participants
are divided into 4 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Hong Kong Baptist University

Lead sponsor

Coburg University of Applied Sciences and Arts

Collaborator

The Hong Kong Polytechnic University

Collaborator

Tung Wah College

Collaborator

Research Grants Council, Hong Kong

Collaborator

Constructor University

Collaborator