Clinical trial registry record

Effects of the Fully Immersive VR Cognitive Training Based on Leisure Activities for the Elderly With MCI and SCD.

A registered study indexed because it matched monitored longevity research terms. Registry status: Unknown. 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 Unknown.
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 May 17, 2021.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT04779671
Last registry update
May 17, 2021
Status
Unknown
Phase
Phase not reported
Sponsor
Chang Gung Memorial Hospital
Enrollment
190
Countries
Taiwan
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

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

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
RANDOMIZED · PARALLEL · TREATMENT · DOUBLE
Evidence population
Human clinical study registration
Participants
190
Population
ALL · 60 Years to 90 Years
Duration
2021-10-01 to 2024-07-01
Intervention
VR cognitive training; Traditional cognitive training
Comparator
control group
Outcomes measured
Change scores of the Montreal Cognitive Assessment (MoCA) — baseline, posttest (around 12 weeks after baseline); Change scores of the Wechsler Memory Scale - Third Edition (WMS-III) — baseline, posttest (around 12 weeks after baseli…; Change scores of Stroop Color-Word Test — baseline, posttest (around 12 weeks after baseline); Change scores of the Wechsler Adult Intelligence Scale (WAIS) — baseline, posttest (around 12 weeks after baseline); Change scores of the Everyday Cognition scales (ECog)-12 items — baseline, posttest (around 12 weeks after baseline); Change scores of the Lawton Instrumental Activities of Daily Living Scale (IADL) — baseline, posttest (around 12 weeks…; Change scores of the WHOQOL-BREF Taiwan Version — baseline, posttest (around 12 weeks after baseline); Change scores of Geriatric Depression Scale (GDS) — baseline, posttest (around 12 weeks after baseline); Change scores of The Chinese Aging Well Profile (CAWP) — baseline, posttest (around 12 weeks after baseline)
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.

  • Cognitive training · 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 50%. These figures help sort records; they are not medical ratings.

cognitive training
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