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 · OTHER · SINGLE
- Evidence population
- Human clinical study registration
- Participants
- 80
- Population
- ALL · 60 Years
- Duration
- 2026-04-30 to 2027-10-30
- Intervention
- AI Chatbot; Control Arm (Educational Preparation Guide)
- Comparator
- Control arm
- Outcomes measured
- Decision regret as assessed by the Decision regret scale — 4 months after surgery; Self-identified health goals following elective hernia surgery, as measured by the Goal Attainment Scale (GAS) — 4 mont…; Decision-making quality in surgical consultations using the Shared Decision-Making Process (SDMP)Scale — 24 hours-72 ho…; Perceived involvement in care using the Perceived Involvement in Care Scale (PICS, binary format) — 24 hours-72 hours a…; Decisional confidence using the SURE scale — 24 hours-72 hours after the intervention; Acceptability as assessed by the Acceptability of Intervention Measure (AIM) — 24 hours-72 hours after the intervention; Appropriateness as assessed by the Intervention Appropriateness Measure (IAM), — 24 hours-72 hours after the interventi…; Feasibility as assessed by the Feasibility of Intervention Measure (FIM) — 24 hours-72 hours after the intervention; Assigned preparation approach on health-related quality of life using the Short Form (SF-12) Quality of Life Scale — 4…; Comfort and function following surgery using the Carolina's Comfort Scale (CCS) — 4 months after surgery; Satisfaction as assessed by the Satisfaction Measure — 24 hours-72 hours after the intervention
- 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 · 80% 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.
- Multimorbidity · 80%Title contains controlled topic terminology. Title supplies ageing or longevity context.
Automated source check 100% · update recency 100%. These figures help sort records; they are not medical ratings.