Clinical trial registry record

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

A registered study indexed because it matched monitored longevity research terms. Registry status: Not Yet Recruiting. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Not Yet Recruiting.
Evidence
Registered phase not reported study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated December 19, 2024.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT06741878
Last registry update
December 19, 2024
Status
Not Yet Recruiting
Phase
Phase not reported
Sponsor
Hong Kong Baptist University
Enrollment
308
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered study indexed because it matched monitored longevity research terms. Registry status: Not Yet Recruiting. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
RANDOMIZED · FACTORIAL · PREVENTION · DOUBLE
Evidence population
Human clinical study registration
Participants
308
Population
ALL · 60 Years to 80 Years
Duration
2025-01-01 to 2026-06-30
Intervention
Exercise; Psychosocial; Nutritional
Comparator
Exercise Training (Biological) + Board Games (Psychosocial) + Diet Consultation (Nutritional); Exercise Training (Biological) + Diet Consultation (Nutritional); Board Games (Psychosocial) + Diet Consultation (Nutritional); Inactive Control (No Treatment)
Outcomes measured
Frailty Status (pre-test) — Pre-test (1st test): before intervention; Frailty Status (2nd test) — 2nd test: after 3-month intervention; Frailty Status (3rd test) — 3rd test: after 6-month follow up; Physical Functioning-- Anthropometic Data (pre-test) — Pre-test (1st test): before intervention; Physical Functioning-- Anthropometric Data (2nd test) — 2nd test: after 3-month intervention; Physical Functioning-- Anthropometric Data (3rd test) — 3rd test: after 6-month follow up; Physical Functioning-- Health Related Information (pre-test) — Pre-test (1st test): before intervention; Physical Functioning-- Health Related Information (2nd test) — 2nd test: after 3-month intervention; Physical Functioning-- Health Related Information (3rd test) — 3rd test: after 6-month follow up; Physical Functioning-- Senior Physical Fitness Test Battery (pre-test) — Pre-test (1st test): before intervention; Physical Functioning-- Senior Physical Fitness Test Battery (2nd test) — 2nd test: after 3-month intervention; Physical Functioning-- Senior Physical Fitness Test Battery (3rd test) — 3rd test: after 6-month follow up; Psychological Functioning (pre-test) — Pre-test (1st test): before intervention; Psychological Functioning (2nd test) — 2nd test: after 3-month intervention; Psychological Functioning (3rd test) — 3rd test: after 6-month follow up; Social Function (pre-test) — Pre-test (1st test): before intervention; Social Function (2nd test) — 2nd test: after 3-month intervention; Social Function (3rd test) — 3rd test: after 6-month follow up; Physical Activity Behavioural Changes (pre-test) — Pre-test (1st test): before intervention; Physical Activity Behavioural Changes (2nd test) — 2nd test: after 3-month intervention
Reported result
No reusable finding-level result is available in this record.

Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.

Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.

Source supportStructured registry protocol metadata; no finding-level conclusion is generated.

Trial stage · Phase not reportedA trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

Registration and recruitment status do not establish safety, efficacy, or regulatory approval.

Why this record appears here · 100% topic match

The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.

  • Frailty · 100%Title contains controlled term: frailty. Abstract contains controlled term: frailty. Source terminology contains: frailty. Title supplies longevity context: frailty, frail. Study type is explicitly identified as INTERVENTIONAL.

Automated source check 100% · update recency 65%. These figures help sort records; they are not medical ratings.