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
- RANDOMIZED · PARALLEL · TREATMENT · NONE
- Evidence population
- Human clinical study registration
- Participants
- 200
- Population
- ALL · 65 Years
- Duration
- 2024-01-29 to 2027-09-30
- Intervention
- Center based attention (stretching only) control; Center based HIIT; Home based HIIT
- Comparator
- Not reported
- Outcomes measured
- Sub-maximal oxygen uptake test (VO2max) — Change from baseline to endpoint at 12 weeks; Cognitive screen - SLUMS — Change from baseline to endpoint at 12 weeks; Amyloid beta 42/40 ratio — Change from baseline to endpoint at 12 weeks; Cognitive screen - Cognivue — Change from baseline to endpoint at 12 weeks; Phosphorylated tau (P-tau) — Change from baseline to endpoint at 12 weeks; Brain Derived Neurotrophic Factor (BDNF) — Change from baseline to endpoint at 12 weeks; Fatigue — Change from baseline to endpoint at 12 weeks; Sleep quantity and stages — Change from baseline to endpoint at 12 weeks; Sleep quality — Change from baseline to endpoint at 12 weeks; Sleep chronotype — Change from baseline to endpoint at 12 weeks; Sleepiness — Change from baseline to endpoint at 12 weeks; Insomnia — Change from baseline to endpoint at 12 weeks; Anxiety and depression — Change from baseline to endpoint at 12 weeks; Sleep disorders — Change from baseline to endpoint at 12 weeks; 30 second chair rise test — Change from baseline to endpoint at 12 weeks; Frailty assessment — Change from baseline to endpoint at 12 weeks; Gait speed — Change from baseline to endpoint at 12 weeks; Arm curl endurance — Change from baseline to endpoint at 12 weeks; Quality of life assessment — Change from baseline to endpoint at 12 weeks; Body Composition (Lean and fat mass) — Change from baseline to endpoint at 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. Source terminology contains: frailty. Title supplies longevity context: frailty, frail. Study type is explicitly identified as INTERVENTIONAL.
Automated source check 100% · update recency 85%. These figures help sort records; they are not medical ratings.