Clinical trial registry record

Tai Chi Versus Conventional Exercise to Improve Cognitive Performance in Older Adults With Mild Cognitive Impairment

A registered study indexed because it matched monitored longevity research terms. Registry status: 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 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 11, 2024.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT05540613
Last registry update
December 11, 2024
Status
Recruiting
Phase
Phase not reported
Sponsor
The University of Hong Kong
Enrollment
315
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: 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
315
Population
ALL · 50 Years
Duration
2022-11-01 to 2026-01-01
Intervention
Health Education; Conventional Exercise; Tai Chi
Comparator
Conventional Exercise
Outcomes measured
The score of the Montreal Cognitive Assessment (MoCA) — 26 weeks; The score of the Montreal Cognitive Assessment (MoCA) — 52 weeks; Clinical Dementia Rating — 26 weeks and 52 weeks; Neurocognitive Test — 26 weeks and 52 weeks; Subjective Cognitive Performance — 26 weeks and 52 weeks; Subjective Memory complaints — 26 weeks and 52 weeks; Subjective Sleep Quality — 26 weeks and 52 weeks; The Hospital Anxiety and Depression Scale — 26 weeks and 52 weeks; The 12-Item Short Form Survey — 26 weeks and 52 weeks; Medication Use — 26 weeks and 52 weeks; Short Physical Performance Battery (SPPB) Test — 26 weeks and 52 weeks; Habitual Physical Activity — 26 weeks and 52 weeks
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.

  • Exercise · 100%Title contains controlled topic terminology. Summary contains controlled topic terminology. Source terminology contains a controlled topic term. Title supplies ageing or longevity context.

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