A registered study indexed because it matched monitored longevity research terms. Registry status: Not Yet Recruiting. Registration does not establish safety or effectiveness.
What the source actually supports
- Evidence stage
- Phase not reported
- Study design
- RANDOMIZED · PARALLEL · HEALTH SERVICES RESEARCH · SINGLE
- Evidence population
- Human clinical study registration
- Participants
- 100
- Population
- ALL · 65 Years
- Duration
- 2025-04-30 to 2026-06-30
- Intervention
- Dual tasks of digital technology
- Comparator
- Control group
- Outcomes measured
- Taiwanese version of the Montreal Cognitive Assessment (MoCA-T) — Baseline, pre-intervention (T0); Taiwanese version of the Montreal Cognitive Assessment (MoCA-T) — Four weeks after intervention(T1=4Weeks); Taiwanese version of the Montreal Cognitive Assessment (MoCA-T) — Eight weeks after intervention(T2=8Weeks); Taiwan Odd-Even Number Sequencing Test (TOENS) — Baseline, pre-intervention (T0); Taiwan Odd-Even Number Sequencing Test (TOENS) — Four weeks after intervention(T1=4Weeks); Taiwan Odd-Even Number Sequencing Test (TOENS) — Eight weeks after intervention(T2=8Weeks); Trail Making Test (TMT) — Baseline, pre-intervention (T0); Trail Making Test (TMT) — Four weeks after intervention(T1=4Weeks); Trail Making Test (TMT) — Eight weeks after intervention(T2=8Weeks); Timed Up and Go (TUG) — Baseline, pre-intervention (T0); Timed Up and Go (TUG) — Four weeks after intervention(T1=4Weeks); Timed Up and Go (TUG) — Eight weeks after intervention; Short Physical Performance Battery (SPPB) — Baseline, pre-intervention (T0); Short Physical Performance Battery (SPPB) — Four weeks after intervention(T1=4Weeks); Short Physical Performance Battery (SPPB) — Eight weeks after intervention; Handgrip strength test — Baseline, pre-intervention (T0); Handgrip strength test — Four weeks after intervention(T1=4Weeks); Handgrip strength test — Eight weeks after intervention(T2=8Weeks)
- 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.
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.
