Effect of KA-EX Supplementation on Recovery Parameters in High-Level Young Football Players

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age17-20
SponsorAntonio Molina Lopez

About this trial

The purpose of this study is to evaluate the effects of KA-EX supplementation on recovery parameters in elite young football players. Athletes from the Udine Primavera team will be randomly assigned to receive either the KA-EX supplement or a sensory-matched placebo immediately following their training sessions for a period of two months.

The researchers will monitor heart rate variability (HRV) and sleep quality using Garmin wearable devices, and assess changes in body composition using Dual-energy X-ray absorptiometry (DEXA) and bioelectrical impedance analysis (BIA). The goal of the study is to determine if post-training KA-EX administration improves physiological recovery, sleep quality, and physical readiness in high-performance athletes during a competitive season.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Membership of the Udine Primavera team at the time of the study. Regular participation in the training programme during the intervention period (September).

Disqualifiers

Presence of any injury or medical condition that limits normal participation in team training sessions.

Trial design

Design model

Parallel

Treatments tested in this trial

  • KA-EX

    Dietary supplement

    Powder sachet to be dissolved in water. Contains a patented complex of amino acids, electrolytes, and carbohydrates designed to normalize cortisol and support recovery.

  • Experimental: KA-EX Supplement

    Dietary supplement

    Powder sachet with identical organoleptic characteristics but without the active recovery ingredients of KA-EX.

Treatment groups

25 Participants
are divided into 2 treatment groups
Group A: KA-EX Group y Placebo Group.Experimental treatment 2 interventions
Group B: Placebo Group.Placebo comparator 2 interventions

Trial outcomes

Primary outcomes

1

Change from Baseline in Heart Rate Variability (rMSSD)

Autonomic recovery assessed as Root Mean Square of Successive Differences (rMSSD) during nocturnal sleep via Garmin wearable devices. Higher values indicate better parasympathetic recovery.

Time frame
Baseline and daily for 8 weeks.

Secondary outcomes

1

Change from Baseline in Sleep Score

Overall sleep quality score calculated by Garmin's proprietary algorithm based on sleep duration, REM, and deep sleep cycles.

Time frame
Daily for 8 weeks.
2

Change from Baseline in Recovery Readiness Index

Daily readiness score (Body Battery) obtained via Garmin wearable algorithm. Scores range from 0 to 100; higher scores indicate greater physical readiness for training.

Time frame
Daily for 8 weeks.
3

Body Composition

Body composition assessed at week 8. Lower values indicate reduction

Time frame
8 weeks.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Antonio Molina Lopez

Lead sponsor

Universidad Pablo de Olavide

Sponsor institution

Universidad Europea de Madrid

Collaborator

University of Udine

Collaborator

Universidad Pablo de Olavide

Collaborator

This trial is not recruiting at the moment. You can still explore other options: