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 · FACTORIAL · SUPPORTIVE CARE · DOUBLE
- Evidence population
- Human clinical study registration
- Participants
- 120
- Population
- ALL · 65 Years to 80 Years
- Duration
- 2019-02-09 to 2021-06-30
- Intervention
- Passive Hypoxia; Normoxia Circuit Training with Elastic Bands; Hypoxia Circuit Training with Elastic Bands; Normoxia Vibration; Hypoxia Vibration
- Comparator
- NorCON; HypCON; NorCIR; NorVIB
- Outcomes measured
- Change from Baseline Life Quality at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Risk of Fall at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Blood Pressure at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Cardiovascular Evaluation at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Cardiovascular Risk at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Weight at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Height at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Body Mass Index at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Waist-Hip Ratio at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Body Composition at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Bone Mineral Density at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Osteoporosis/Osteopenia Prevalence at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Bone Mineral Content at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Biochemical Parameters at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Bone Remodelling Markers at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Inflammatory Markers at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Endothelial Markers at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Lower Limb Strength at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Upper Limb Strength at 24 weeks — Through study completion, an average of 24 weeks; Change from Baseline Lower Limb Flexibility at 24 weeks — Through study completion, an average of 24 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.
- Resistance training · 100%Title contains controlled term: strength training. Abstract contains controlled term: resistance training, strength training. Title supplies longevity context: elderly. Study type is explicitly identified as INTERVENTIONAL.
Automated source check 100% · update recency 50%. These figures help sort records; they are not medical ratings.