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
- OBSERVATIONAL
- Evidence population
- Human clinical study registration
- Participants
- 56
- Population
- ALL · 70 Years
- Duration
- 2026-04-02 to 2026-06-01
- Intervention
- Multicomponent Exercise Program- 1 times per week.; Multicomponent Exercise Program- 2 times per week.
- Comparator
- Not reported
- Outcomes measured
- Change in Physical Performance Short Physical Performance Battery (SPPB) — Baseline (T0) and post-intervention (8-12 we…; Change in Fall Risk — Baseline (T0) and post-intervention (8-12 weeks); Change in Instrumented Balance: Center of Pressure (CoP) Sway Area — Baseline (T0) and post-intervention (8-12 weeks); Change in Instrumented Balance: Center of Pressure (CoP) Velocity — Baseline (T0) and post-intervention (8-12 weeks); Change in Instrumented Balance:Center of Pressure (CoP) Path Length. — Baseline (T0) and post-intervention (8-12 weeks); Functional Performance: Change in Timed Up and Go (TUG) Test — Baseline (T0) and post-intervention (8-12 weeks); Functional Performance: Change in Gait Speed (4-Meter Walk Test) — Baseline (T0) and post-intervention (8-12 weeks); Functional Performance: Change in FRAIL Scale Score — Baseline (T0) and post-intervention (8-12 weeks); Muscle Strength: Change in Handgrip Strength — Baseline (T0) and post-intervention (8-12 weeks); Muscle Strength: Change in 30-Second Sit-to-Stand Test — Baseline (T0) and post-intervention (8-12 weeks); Balance — Baseline (T0) and post-intervention (8-12 weeks); Aerobic Capacity — Baseline (T0) and post-intervention (8-12 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 · 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. Title supplies longevity context: frailty, frail. Study type is explicitly identified as OBSERVATIONAL.
Automated source check 100% · update recency 100%. These figures help sort records; they are not medical ratings.