Clinical trial registry record

Targeted Prehabilitation With Physical Exercise and Inspiratory Muscle Training for Elderly Frail Patients Prior to Ventral Hernia Repair

A registered study indexed because it matched monitored longevity research terms. Registry status: Enrolling By Invitation. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Enrolling By Invitation.
Evidence
Registered phase not reported study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated May 27, 2026.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT06874413
Last registry update
May 27, 2026
Status
Enrolling By Invitation
Phase
Phase not reported
Sponsor
Prisma Health-Upstate
Enrollment
120
Countries
United States
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered study indexed because it matched monitored longevity research terms. Registry status: Enrolling By Invitation. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
RANDOMIZED · PARALLEL · TREATMENT · NONE
Evidence population
Human clinical study registration
Participants
120
Population
ALL · 65 Years
Duration
2025-03-19 to 2027-06-30
Intervention
Prehabilitation; Standard of Care (SOC)
Comparator
Group 1 - Standard of Care; Group 3 - Observational Cohort
Outcomes measured
Activity levels — 6-8 weeks preoperatively; Quality of Life Pre- and Postoperative Assessment — 14-30 days postoperatively; Quality of Life Pre- and Postoperative Outcomes — 14-30 days postoperatively; Postoperative Outcomes - Surgical Complications — 14-30 days postoperatively; Postoperative Outcomes - Length of Stay — 14-30 days postoperatively; Postoperative Outcomes - Discharge Location — 14-30 days postoperatively; Postoperative Outcomes - Return to Baseline — 14-30 days postoperatively
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.

Trial stage · Phase not reportedA trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

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 term: exercise. Abstract contains controlled term: exercise. Title supplies longevity context: frail, elderly. Study type is explicitly identified as INTERVENTIONAL.

Automated source check 100% · update recency 100%. These figures help sort records; they are not medical ratings.

exercise
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