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Effects of a Recovery Supplement on Body Composition, Performance, Muscular Properties, and Wellbeing

Not Applicable
Completed
Conditions
Psychological
Protein Deficiency
Fatigue
Muscular Atrophy
Training Group, Sensitivity
Interventions
Dietary Supplement: Ingestion of a Maltodextrin Supplement
Dietary Supplement: Ingestion of a Post-Workout Supplement
Registration Number
NCT05769101
Lead Sponsor
Joel Puente
Brief Summary

The investigation will be conducted as a double blinded, randomized, parallel between treatment conditions comparison design with two different groups ingesting a different supplement each one.

Detailed Description

Following inclusion, familiarization and baseline assessments, the participants will be randomly allocated to receive either a multi-ingredient, post-workout supplement (REC) or maltodextrin (CHO). Thereafter, the participants will follow a 6-weeks resistance training mesocycle, involving three resistance training sessions (Monday, Wednesday and Friday) per week (18 sessions in total). Before and after the 6 weeks of intervention, the following assessments will be performed: (i) Body composition (fat mass and fat-free mass) via air displacement plethysmography (BodPod); (ii) muscle contractile properties on Vastus Medialis and Anterior Deltoids (via Tensiomyography; (iii) muscle structure of the Vastus Lateralis of the Quadriceps and the Elbow Flexors of dominant extremities via Ultrasound; (iv) Maximal Isometric Strength (Isometric Mid-Thigh Pull); (v) Upper and Lower Body Muscular Power (Medicine Ball Throw and Vertical Jump), (vi) Upper and Lower Muscular Endurance (30- Seconds Sit-to-Stand and 30-Seconds 16RM Bench Press), (vii) Immune System (via HemoCue WBC DIFF System).

The supplements will be ingested immediately (within 15 min) after each training session.

Energy Feeling Questionnaire will be filled immediately before warming up.

In addition, Rate of Perceived Exertion to training will be assessed 15 min after the completion of all workouts.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Healthy (no injuries, illnesses or medication intake).
  • Between 45 and 65 years old.
  • Active and familiarised with Resistance Training.
Exclusion Criteria
  • Unhealthy (illnesses or medication intake) or injured.
  • Untrained.
  • Young (<45 y.o.) or elderly (>65 y.o.).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Maltodextrin SupplementIngestion of a Maltodextrin SupplementAn isoenergetic Maltodextrin supplement will be administered as placebo. Dissolved in 350 ml of water.
Multi-Ingredient Post-Workout SupplementIngestion of a Post-Workout SupplementA 60 g dose of a commercially available Recovery supplement providing \~205 kcal including Proteins (+EAA), Carbohydrates, Creatine, and Vitamin D. Diluted in 350 ml of water.
Primary Outcome Measures
NameTimeMethod
Vertical JumpChanges from 3 days previous to, and 3 days after the completion of the 6-weeks training program

Height (measured in centimetres)

Muscle ThicknessChanges from 3 days previous to, and 3 days after the completion of the 6-weeks training program

Thickness of the Vastus Lateralis and the Elbow Flexors of the dominant limbs

Self Perceived Energy Feeling[Time Frame: Changes from 3 days previous to, and 3 days after the completion of the 6-weeks training program]

All participants will fill a short questionnaire (from 1 to 5 points) about their perception of energy before every training. Energy Feeling will be assessed (Evergy level, Fatigue Level, Feeling of Alertness, and Feeling of Focus for the task, valued from 1 = low energy to 5 = high energy).

White Blood Cells countChanges from 3 days previous to, and 3 days after the completion of the 6-weeks training program

White blood cell (WBC) count including a five-part differential

Chest Medicine Ball ThrowChanges from 3 days previous to, and 3 days after the completion of the 6-weeks training program

Distance (measured in centimetres)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Greenwich, Avery Hill Campus, Sparrows Farm. Avery Hill, London., United Kingdom, SE9 2BT

🇬🇧

London, Avery Hill, London., United Kingdom

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