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 · TREATMENT · SINGLE
- Evidence population
- Human clinical study registration
- Participants
- 70
- Population
- ALL · 60 Years
- Duration
- 2024-10-31 to 2026-02-27
- Intervention
- Physical exercise program; Neural mobilization techniques
- Comparator
- Physical exercise
- Outcomes measured
- Pain Severity — T0: baseline assessment; T1: 10 weeks (post-intervention assessment); T2: 3 months post-intervention (f…; Temporal characteristics of pain — T0: baseline assessment; T1: 10 weeks (post-intervention assessment); T2: 3 months p…; Neuropathic pain components — T0: baseline assessment; T1: 10 weeks (post-intervention assessment); T2: 3 months post-i…; Pain Catastrophizing — T0: baseline assessment; T1: 10 weeks (post-intervention assessment); T2: 3 months post-interven…; Fear of Movement — T0: baseline assessment; T1: 10 weeks (post-intervention assessment); T2: 3 months post-intervention…; Signs and symptoms of hypersensitivity of the nervous system — T0: baseline assessment; T1: 10 weeks (post-intervention…; Pressure Pain Threshold measured in three different sites (thenar region of the dominant hand; dorsum of foot on domina…; Q-sense - Cold and Warm Perception Threshold (thenar region of the dominant hand; dorsum of foot on dominant side; regi…; Q-sense - Heat Pain Threshold (thenar region of the dominant hand; dorsum of foot on dominant side; region of greatest…; Lower Limb Strength — T0: baseline assessment; T1: 10 weeks (post-intervention assessment); T2: 3 months post-intervent…; Grip Strength — T0: baseline assessment; T1: 10 weeks (post-intervention assessment); T2: 3 months post-intervention (f…; Balance — T0: baseline assessment; T1: 10 weeks (post-intervention assessment); T2: 3 months post-intervention (follow-…
- 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 85%. These figures help sort records; they are not medical ratings.