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 · DOUBLE
- Evidence population
- Human clinical study registration
- Participants
- 150
- Population
- ALL · 40 Years to 80 Years
- Duration
- 2023-09-15 to 2025-05-01
- Intervention
- core stabilization exercise
- Comparator
- waiting list control group
- Outcomes measured
- The Oswestry Low Back Pain Disability Questionnaire — pre-intervention session (T1); The Oswestry Low Back Pain Disability Questionnaire — post-intervention (8 weeks after start of intervention;T2); Visual analogue scale (VAS) score for pain — pre-intervention session (T1); Visual analogue scale (VAS) score for pain — post-intervention (8 weeks after start of intervention;T2); Fear-Avoidance Belief Questionnaire — pre-intervention session (T1); Fear-Avoidance Belief Questionnaire — post-intervention (8 weeks after start of intervention;T2); Surface EMG — pre-intervention session (T1); Surface EMG — post-intervention (8 weeks after start of intervention;T2); IMU-sensor — pre-intervention session (T1); IMU-sensor — post-intervention (8 weeks after start of intervention;T2); Prone instability test — pre-intervention session (T1); Prone instability test — post-intervention (8 weeks after start of intervention;T2); straight leg raise (SLR) — pre-intervention session (T1); straight leg raise (SLR) — post-intervention (8 weeks after start of intervention;T2); internal rotation range of motion — pre-intervention session (T1); internal rotation range of motion — post-intervention (8 weeks after start of intervention;T2); FABER test — pre-intervention session (T1); FABER test — post-intervention (8 weeks after start of intervention;T2)
- 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 100%. These figures help sort records; they are not medical ratings.
