A registered study indexed because it matched monitored longevity research terms. Registry status: Recruiting. Registration does not establish safety or effectiveness.
What the source actually supports
- Evidence stage
- Phase not reported
- Study design
- NON RANDOMIZED · SINGLE GROUP · PREVENTION · NONE
- Evidence population
- Human clinical study registration
- Participants
- 225
- Population
- ALL · 65 Years
- Duration
- 2024-06-06 to 2026-11-01
- Intervention
- Volunteer-led physical activity
- Comparator
- Control
- Outcomes measured
- Qualitative interview data exploring the acceptability of the intervention, including barriers and enablers to the impl…; The number of volunteers recruited to the study (%). — through study completion, an average of 3 years; Number of trainers trained in each hospital site (%) — through study completion, an average of 3 years; Adherence to the intervention (%) — through study completion, an average of 3 years; Recruitment rate (%) of participants in each site — through study completion, an average of 3 years; The number of volunteers trained at the end of the study period (%) — through study completion, an average of 3 years; The number of volunteers retained at the end of the study period (%) — through study completion, an average of 3 years; Number of trainers retained in each hospital site (%) — through study completion, an average of 3 years; Patient's subjective assessment of quality of life - visual analogue scale (VAS) — Baseline and post intervention, an a…; Grip strength — Baseline and post intervention, an average of 2 months; Short Physical Performance Battery (SPPB) — Baseline and post intervention, an average of 2 months; Physical activity — 7 days upon recruitment; Patient's subjective assessment of quality of life - EuroQol (EQ-5D-5L) — Baseline and post intervention, an average of…
- 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.
- 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 100%. These figures help sort records; they are not medical ratings.