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Evaluation of the Effects of a Novel Dietary Microalgae Based Ingredient on Muscle Recovery and Endurance Capacity

Evaluation of the Protective Effects of a Novel Dietary Microalgae Supplement (PeLiv) Following Exercise-induced Muscle Damage and Influence on Endurance Capacity After Prolonged Consumption

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05760742
Acronym
PORPHY-ONE
Enrollment
80
Registered
2023-03-08
Start date
2023-01-10
Completion date
2023-08-18
Last updated
2023-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

recovery, muscle endurance, exercise capacity, microalgae, inflammation

Brief summary

The purpose of this investigation is to examine the effects of consuming a new dietary microalgae based supplement vs. placebo on neuromuscular function, energy utilization, soreness, perceptual wellness, swelling, and markers of muscle damage and inflammation in healthy young men before and after an acute exercise-induced muscle damage protocol (downhill running), and influence on endurance capacity after prolonged consumption.

Interventions

DIETARY_SUPPLEMENTMicAlgae

2 months of supplementation with an innovative microalgae based ingredient

DIETARY_SUPPLEMENTPlacebo

2 months of supplementation with a placebo (Maltodextrin)

Sponsors

University of Central Florida
CollaboratorOTHER
Microphyt
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Male participants * Healthy as assessed by Medical and activity history questionnaire (MHQ) * Recreationally active according to American College of Sports Medicine guidelines * Able to provide written and dated informed consent to participate in the study

Exclusion criteria

* Untrained * Any response of yes on the PAR-Q+ * Physical limitations preventing running, countermovement jump, and strength (peak isometric torque and peak isokinetic torque) assessments

Design outcomes

Primary

MeasureTime frameDescription
Neuromuscular functionFrom 0 to week 4isokinetic peak torque in Newton per meter (N/m)

Secondary

MeasureTime frameDescription
Soreness and perceptual wellnessFrom 0 to week 4Evaluated using using a 100-point numerical pain rating scale anchored with 0= no pain to 100= the most intense pain sensation imaginable after exercise-induced muscle damage protocol
Energy utilization (Oxygen consumption - VO2)From 0 to week 4Running economy during a 5-minute run at 80% of the speed at VO2max with gaz exchange analyzis
Isokinetic neuromuscular functionFrom 0 to week 8peak torque in Newton per meter (N/m)
Isometric neuromuscular functionFrom 0 to week 8peak torque in Newton per meter (N/m)
Swelling - Muscle thickness (mm or cm)From 0 to week 4Evaluated using musculoskeletal ultrasound
Swelling - overall thigh circumference (mm or cm)From 0 to week 4Evaluated using musculoskeletal ultrasound
Endurance capacityFrom 0 to week 4Maximal oxygen consumption (VO2max) determined during graded exercise test
lactate dehydrogenase (U/L)After 4 weeks of supplementationBlood marker analyzis
Myoglobin (ug/l)After 4 weeks of supplementationBlood marker analyzis
Interleukin-6 (pg/ml)After 4 weeks of supplementationBlood marker analyzis - inflammation
Tumor necrosis factor-α (ug/ml)After 4 weeks of supplementationBlood marker analyzis - inflammation
C-reactive protein (mg/l)After 4 weeks of supplementationBlood marker analyzis - inflammation
Isometric Neuromuscular functionFrom 0 to week 4Peak torque in Newton per meter (N/m)
Creatine kinase (UI/I)After 4 weeks of supplementationBlood marker analyzis

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026