A registered study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.
What the source actually supports
- Evidence stage
- Phase not reported
- Study design
- RANDOMIZED · PARALLEL · PREVENTION · SINGLE
- Evidence population
- Human clinical study registration
- Participants
- 63
- Population
- ALL · 45 Years to 80 Years
- Duration
- 2020-08-30 to 2024-08-15
- Intervention
- Executive function (EF) training
- Comparator
- Wait-list control
- Outcomes measured
- Pre-training Change in auditory 2-back accuracy — baseline; Post-training Change in auditory 2-back accuracy — after 12 weeks; Pre-training Change in auditory 2-back reaction time — baseline; Post-training Change in auditory 2-back reaction time — after 12 weeks; Pre-training Multi-Talker word perception (accuracy) — baseline; Post-training Multi-Talker word perception (accuracy) — after 12 weeks; Pre-training Change in stride time (mean, standard deviation [SD] of stride time) — baseline; Post-training Change in stride time (mean, standard deviation [SD] of stride time) — after 12 weeks; Pre-training Change in stride time variability (mean, standard deviation [SD] of stride time) — baseline; Post-training Change in stride time variability (mean, standard deviation [SD] of stride time) — after 12 weeks; Pre-training Montreal Cognitive Assessment (MoCA) — baseline; Post-training Montreal Cognitive Assessment (MoCA) — after 12 weeks; Pre-training WAIS-IV Digit Symbol Coding — baseline; Post-training WAIS-IV Digit Symbol Coding — after 12 weeks; Pre-training Trail Making Test — baseline; Post-training Trail Making Test — after 12 weeks; Pre-training D-KEFS Stroop — baseline; Post-training D-KEFS Stroop — after 12 weeks; Pre-training Rey Auditory Verbal Learning Test — baseline; Post-training Rey Auditory Verbal Learning Test — after 12 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.
Registration and recruitment status do not establish safety, efficacy, or regulatory approval.
Why this record appears here · 80% 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 · 80%Title contains controlled topic terminology. Title supplies ageing or longevity context.
Automated source check 100% · update recency 65%. These figures help sort records; they are not medical ratings.