Clinical trial registry record

VICIA FABA PEPTIDES AND RESISTANCE TRAINING IN THE ELDERLY

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 October 5, 2026.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT07858292
Last registry update
October 5, 2026
Status
Enrolling By Invitation
Phase
Phase not reported
Sponsor
Universidade Cesumar (UNICESUMAR)
Enrollment
77
Countries
Brazil
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 · PREVENTION · TRIPLE
Evidence population
Human clinical study registration
Participants
77
Population
ALL · 60 Years
Duration
2026-11-01 to 2027-01-01
Intervention
Vicia faba L.-derived peptides; Placebo; Supervised Resistance Training
Comparator
Physically Active + Placebo; Physically Inactive + Placebo
Outcomes measured
Fat-Free Mass — Baseline and after 4 weeks of intervention; Handgrip Strength — Baseline and after 4 weeks of intervention; Maximal Voluntary Isometric Contraction and Muscle Power during Knee Extension and Flexion — Baseline and after 4 weeks…; Lower-Limb Strength Endurance — Baseline and after 4 weeks of intervention; Upper-Limb Muscle Power — Baseline and after 4 weeks of intervention; Dynamic Balance — Baseline and after 4 weeks of intervention; Self-Reported Functional Disability — Baseline and after 4 weeks of intervention; Body fat percentage — Baseline and after 4 weeks of intervention; Vastus Lateralis and Rectus Femoris Muscle Thickness — Baseline and after 4 weeks of intervention; Physical Frailty — Baseline and after 4 weeks of intervention; Intensity of Depressive Symptoms — Baseline and after 4 weeks of intervention; Quality of Life — Baseline and after 4 weeks of 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.

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.

  • Resistance training · 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.