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Not yet recruiting NCT06741878

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

No phase Interventional Frailty in Older Adults

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exercise, Psychosocial, Nutritional.
Who it may be relevant to
Registry conditions: Frailty in Older Adults. Basic parameters: 60 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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.

Detailed description

The study will be designed as a four-arm, double-blinded, cluster-randomised controlled trial. A sample (N = 308) of prefrail older adults aged 60-80 years will be recruited from 32 randomly selected elderly community centres in Hong Kong and classified into four frailty deficit patterns (multi-frailty, physical-to-psycho/social, nonphysical-to-psycho/social, and a robust control). With the hypothesised biopsychosocial framework pinpointing the intertwined relationships of these three domains of frailty, four intervention strategies (biological/psychosocial/nutritional, biological/nutritional, psychosocial/nutritional, and an inactive control) will be proposed to improve their overall frailty, regarding their physical, psychological, and social functioning, nutritional status, and lifestyle changes in a 9-month intervention and follow-up period. The primary objective will be to assess the effectiveness of the intervention strategies for improving the frailty status of participants in each of the four frailty deficit pattern groups, and to determine the most effective intervention strategy.

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.

Primary outcome measures

  • Frailty Status (pre-test) [Time frame: Pre-test (1st test): before intervention]
  • Frailty Status (2nd test) [Time frame: 2nd test: after 3-month intervention]
  • Frailty Status (3rd test) [Time frame: 3rd test: after 6-month follow up]
  • Physical Functioning-- Anthropometic Data (pre-test) [Time frame: Pre-test (1st test): before intervention]
  • Physical Functioning-- Anthropometric Data (2nd test) [Time frame: 2nd test: after 3-month intervention]
  • Physical Functioning-- Anthropometric Data (3rd test) [Time frame: 3rd test: after 6-month follow up]
  • Physical Functioning-- Health Related Information (pre-test) [Time frame: Pre-test (1st test): before intervention]
  • Physical Functioning-- Health Related Information (2nd test) [Time frame: 2nd test: after 3-month intervention]
  • Physical Functioning-- Health Related Information (3rd test) [Time frame: 3rd test: after 6-month follow up]
  • Physical Functioning-- Senior Physical Fitness Test Battery (pre-test) [Time frame: Pre-test (1st test): before intervention]
Secondary outcome measures (12)
  • Physical Activity Behavioural Changes (pre-test) [Time frame: Pre-test (1st test): before intervention]
  • Physical Activity Behavioural Changes (2nd test) [Time frame: 2nd test: after 3-month intervention]
  • Physical Activity Behavioural Changes (3rd test) [Time frame: 3rd test: after 6-month follow up]
  • Exercise Self-efficacy (pre-test) [Time frame: Pre-test (1st test): before intervention]
  • Exercise Self-efficacy (2nd test) [Time frame: 2nd test: after 3-month intervention]
  • Exercise Self-efficacy (3rd test) [Time frame: 3rd test: after 6-month follow up]
  • Nutrition Self-efficacy (pre-test) [Time frame: Pre-test (1st test): before intervention]
  • Nutrition Self-efficacy (2nd test) [Time frame: 2nd test: after 3-month intervention]
  • Nutrition Self-efficacy (3rd test) [Time frame: 3rd test: after 6-month follow up]
  • Nutritional Status (pre-test) [Time frame: Pre-test (1st test): before intervention]
  • Nutritional Status (2nd test) [Time frame: 2nd test: after 3-month intervention]
  • Nutritional Status (3rd test) [Time frame: 3rd test: after 6-month follow up]

Eligibility criteria

Inclusion criteria

  • 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)
  • Can walk independently to an elderly centre
  • Have a smartphone for internal group communication and remote interaction with their peers and the instructor

Exclusion criteria

  • 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
  • Currently undergoing exercise programmes or classified as physically 'very active' (i.e. performing strenuous activity for 5+ hours each week)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Factorial
Masking
Double blind
Primary purpose
Prevention

Study locations

Center list to be confirmed — check the primary protocol.

Publications

  • Jiao J, Man DW, Lippke S, Hassel H, Tam BT, Chan CH, Ng YL, Lo KK. A biopsychosocial approach to improving multidimensional frailty status in community-dwelling older adults: a protocol for a cluster randomized controlled trial. BMC Geriatr. 2025 Jul 15;25(1):530. doi: 10.1186/s12877-025-06053-x. PMID 40665217

Identifiers

NCT: NCT06741878 · 12600824

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗