Clinical trial registry record

Effects of Music-with-Movement on Cognitive and Physical Performance of People With Potentially Reversible Cognitive Frailty: a Randomised Controlled Trial

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 February 13, 2025.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT06791720
Last registry update
February 13, 2025
Status
Not Yet Recruiting
Phase
Phase not reported
Sponsor
The Hong Kong Polytechnic University
Enrollment
113
Countries
Hong Kong
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 · PARALLEL · TREATMENT · SINGLE
Evidence population
Human clinical study registration
Participants
113
Population
ALL · 60 Years
Duration
2025-03-01 to 2027-12-31
Intervention
music-based cognitive-motor dual-task training/exercise; Social Gatherings
Comparator
Not reported
Outcomes measured
Montreal Cognitive Assessment — Change from baseline to 28 weeks after programme; Frontal Assessment Battery — Change from baseline to 28 weeks after programme; Fuld Object Memory Evaluation — Change from baseline to 28 weeks after programme; Modified Fuld Verbal Fluency Test — Change from baseline to 28 weeks after programme; Social Participation Quesionnaire — Change from baseline to 28 weeks after programme; Subjective Happiness Scale — Change from baseline to 28 weeks after programme; DeJong Gierveld Loneliness Scale — Change from baseline to 28 weeks after programme; Edmonton Frail Scale — Change from baseline to 28 weeks after programme; Timed Up and Go Test — Change from baseline to 28 weeks after programme; Handgrip Strength — Change from baseline to 28 weeks after programme; Six-minute Walk Test — Change from baseline to 28 weeks after programme
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.

frailty
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