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 · SINGLE
- Evidence population
- Human clinical study registration
- Participants
- 44
- Population
- ALL · 65 Years
- Duration
- 2026-04-01 to 2026-12-01
- Intervention
- Aquatic Exercise Program; Home Exercise Program
- Comparator
- Home Exercise Only Group
- Outcomes measured
- Five Times Sit to Stand Test — Baseline, immediately after the 6-week intervention, and 1 month post-treatment follow-up; Sonographic Thigh Adjustment Ratio (STAR) — Baseline, immediately after the 6-week intervention, and 1 month post-treat…; Handgrip Strength — Baseline, immediately after the 6-week intervention, and 1 month post-treatment follow-up; Anterior Thigh Muscle Thickness — Baseline, immediately after the 6-week intervention, and 1 month post-treatment follo…; Appendicular Skeletal Muscle Mass Index (ASM/height²) — Baseline, immediately after the 6-week intervention, and 1 mont…; 4-Meter Gait Speed Test — Baseline, immediately after the 6-week intervention, and 1 month post-treatment follow-up; Short Physical Performance Battery (SPPB) — Baseline, immediately after the 6-week intervention, and 1 month post-treat…; Berg Balance Scale — Baseline, immediately after the 6-week intervention, and 1 month post-treatment follow-up; Timed Up and Go (TUG) Test — Baseline, immediately after the 6-week intervention, and 1 month post-treatment follow-up; Geriatric Depression Scale (GDS) — Baseline, immediately after the 6-week intervention, and 1 month post-treatment foll…; SF-36 Quality of Life Scale — Baseline, immediately after the 6-week intervention, and 1 month post-treatment follow-up
- 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.
- Sarcopenia · 100%Title contains controlled term: sarcopenia. Abstract contains controlled term: sarcopenia. Source terminology contains: sarcopenia. Title supplies longevity context: older adult. Study type is explicitly identified as INTERVENTIONAL.
Automated source check 100% · update recency 100%. These figures help sort records; they are not medical ratings.