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 · NONE
- Evidence population
- Human clinical study registration
- Participants
- 39
- Population
- ALL · 70 Years
- Duration
- 2018-05-16 to 2021-03-01
- Intervention
- PRISME-3P program
- Comparator
- Non interventional
- Outcomes measured
- Change in Short Physical Performance Battery (SPPB) score — from baseline at 6 months; Evolution of the Short Physical Performance Battery (SPPB) score — Baseline, 3 months (for interventional arm), 6 month…; Assessment of functional disability by questionnaires — Baseline, 6 months and 12 months; Assessment of Quality of Life by questionnaire — baseline, 6 months and 12 months; Number of falls — Baseline, 6 months and 12 months; Number of hospitalization — Baseline, 6 months and 12 months; Assessment of the Physical Activity by questionnaire — baseline, 6 months and 12 months; Assessment of sedentary time by questionnaire — baseline, 6 months and 12 months; Assessment of weight loss — baseline, 6 months and 12 months; Body Mass Index (BMI) — baseline, 6 months and 12 months; Assessment of nutritional status using MNA scale — baseline, 3 months (for interventional arm depending on the SPPB sco…; Rate of study participation — Baseline; Monitoring of detailed physical activity performed by patients with diaries outlining the exercise sessions . — at the…; Monitoring of detailed physical activity performed by patients with MAPA assessment. — at the end of the multimodal int…; Rate of compliant General practitioners (GP) associated to the study — at 12 months; Assessment of psychological factors using GDS-4 scale associated with a loss of mobility — baseline, 6 and 12 months; Assessment of social factors associated with a loss of mobility — baseline; Assessment of comorbidities using the index of Charlson — baseline; Description of concomitant medications — baseline; Type of diagnoses for unknown diseases following the dedicated geriatric consultation. — baseline
- 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. Title supplies ageing or longevity context.
Automated source check 100% · update recency 85%. These figures help sort records; they are not medical ratings.