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

NCT06741878 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 308

Last updated 2024-12-19

No results posted yet for this study

Summary

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.

Conditions

  • Frailty in Older Adults

Interventions

BEHAVIORAL

Exercise

Involves participants engaging in physical training group sessions in light-to-moderate intensity.

BEHAVIORAL

Psychosocial

Involves participants engaging in selected board and card games which require cognitive and socialization skills to play in a group setting of 2-4 people.

BEHAVIORAL

Nutritional

Involves participants attending dietary classes taught by a certified dietitian, including individualized consultation.

Sponsors & Collaborators

  • Coburg University of Applied Sciences and Arts

    collaborator UNKNOWN
  • The Hong Kong Polytechnic University

    collaborator OTHER
  • Tung Wah College

    collaborator OTHER
  • Research Grants Council, Hong Kong

    collaborator OTHER
  • Constructor University

    collaborator UNKNOWN
  • Hong Kong Baptist University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
FACTORIAL

Eligibility

Min Age
60 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-01-01
Primary Completion
2026-03-31
Completion
2026-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06741878 on ClinicalTrials.gov