Long-term Intervention Effects of a Personalized, Home-based Exercise Program and Nutritional Advice, Along With the Inclusion of a Pre-workout Multi-ingredient Supplement on the Body Composition, Functional Capacity and Quality of Life of Middle-aged and Older Adults (40-70 Years)

December 14, 2021 updated by: Joel Puente, University of Greenwich
The purpose of this study is to analyse the potential benefits of ingesting a commercially available pre-workout multi-ingredient supplement providing ~90 Kcal. for 25g of powder: carbohydrates -isomaltulose, fructose, maltodextrin- 15 g, essential amino-acids -Beta-alanine -L-arginine AKG, L-Leucine, Taurine, L-citrulline- 6.8 g, Creatine monohydrate: 2g, Guarana Extract: 800mg, total caffeine: 160mg, and Magnesium: 112.5mg) vs Placebo CHO intake on body composition, physical performance, Happiness Score (specially designed by our sponsor company, including different self-reported and validated tests on their short form) and every workout: Self-perceived energy feeling and adherence to the intervention.

Study Overview

Detailed Description

The methodology will follow a Home-based, online, double-blinded, randomised, long-term design. The participants recruited will be active, middle-aged and older healthy adults. The supplement intake will be a Pre-workout supplement intake or a placebo intake. The exercise training will be a Progressive Resistance Training, with sessions of ~1 hour (3 times/week). The intervention will last for a minimum of one year and the possibility to prolong it to another one (two years of intervention) if the adherence to the treatment was higher to the 75% of the participants (of, at least, 85% of the training sessions and supplementation intake).

The outcomes that will be assessed are: Body composition (fat mass and fat-free mass), physical performance (short test designed by Go Fit Lab: single-leg standing balance, upper-body strength - maximum number of push-ups repetitions in 15 seconds -, lower-body mechanical power - vertical jump -, agility/velocity - 30 seconds of static running at maximum velocity -, recovery assessment - 60 seconds monitoring of heart rate after the previous test -), Happiness Score (designed by Go Fit, including different self-reported validated tests, such as: Par-Q+, ACSM Cardiovascular Risk Factors Questionnaire, SF-12 for quality of life and self-perceived health status, PSS-4 Stress and mental health, Pittsburgh Sleeping Quality test, PREDIMED test: adherence to Mediterranean diet eating patterns, and the IPAQ short form), and for every workout: Self-perceived energy feeling (Questionnaire: Energy Level, Fatigue, Alertness and Focus for the Task), Rate of Perceived Exertion (OMNI RES Scale and Borg Scale) and adherence to regular physical exercise practise, healthy nutritional patterns, and supplement intake.

Study Type

Interventional

Enrollment (Anticipated)

3000

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Joel Puente Fernández, PhD Student
  • Phone Number: +34626610821
  • Email: jp2979a@gre.ac.uk

Study Contact Backup

Study Locations

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

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

40 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Healthy adults (no current injuries or illnesses which may interfere with the project).
  • Recreationally active adults (a minimum of 3 and a maximum of 5 days of training sessions per week: combining resistance and endurance).

Exclusion Criteria:

  • Participants younger than 40 or older than 70 years old.
  • Participants with hard injuries, disabilities or pathologies.
  • People taking medication or other supplements which may interfere with the multi-ingredient pre-workout or the training sessions.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Multi-Ingredient Pre-workout Supplement

This group of participants will intake a multi-ingredient supplement around ~15 minutes before every workout.

The nutritional information of the supplement is: ~90 Kcal. for 25g of powder: carbohydrates -isomaltulose, fructose, maltodextrin- 15 g, essential amino-acids -Beta-alanine: 2.5g, L-arginine AKG: 2.5g, L-Leucine: 800mg, Taurine: 500mg, L-citrulline: 500mg- 6.8 g, Creatine monohydrate: 2.0g, Guarana Extract: 800mg, total caffeine: 160mg, and Magnesium: 112.5mg.

They will also follow a previously designed progressive resistance training (3 times a week, around 1 hour a day, consisting of different exercises).

Also, they will receive a specific guideline with simple tips to improve their nutritional patterns.

The training sessions and the nutritional guideline will be the same for the three groups.

Every important issue has been detailed before.
Other Names:
  • Preworkout
The information about it has been detailed in advance.
Other Names:
  • RT
  • PRT
This intervention has also been described in advance.
Other Names:
  • Nutrition
  • Healthy Eating
Active Comparator: Isocaloric Placebo

This group of participants will intake an isocaloric (only carbohydrates: Maltodextrin) supplement comparator, around ~15 minutes before every workout.

The nutritional information of the supplement is: ~90 Kcal. for 23g of powder.

They will also follow a previously designed progressive resistance training (3 times a week, around 1 hour a day, consisting of different exercises).

Also, they will receive a specific guideline with simple tips to improve their nutritional patterns.

The training sessions and the nutritional guideline will be the same for the three groups.

The information about it has been detailed in advance.
Other Names:
  • RT
  • PRT
This intervention has also been described in advance.
Other Names:
  • Nutrition
  • Healthy Eating
Sham Comparator: Control

These participants will drink a non-caloric admixture with the same taste, texture and flavour.

They will also follow a previously designed progressive resistance training (3 times a week, around 1 hour a day, consisting of different exercises).

Also, they will receive a specific guideline with simple tips to improve their nutritional patterns.

The training sessions and the nutritional guideline will be the same for the three groups.

The information about it has been detailed in advance.
Other Names:
  • RT
  • PRT
This intervention has also been described in advance.
Other Names:
  • Nutrition
  • Healthy Eating

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Fat Mass
Time Frame: Through study completion, an average of 1 year.
Assessment of the total adipose tissue via Bioelectrical Impedance.
Through study completion, an average of 1 year.
Fat-free Mass
Time Frame: Through study completion, an average of 1 year.
Assessment of the total lean mass via Bioelectrical Impedance.
Through study completion, an average of 1 year.
Health Perception questionnaire
Time Frame: 6 weeks.

Short Form of 12 questions.

Higher scores mean better outcomes (score from 0 to 100).

6 weeks.
Pittsburgh Sleep Quality Index
Time Frame: 6 weeks.

Short Form of 4 questions.

Higher scores mean better outcomes (score from 1 to 5).

6 weeks.
Stress Level and Mental Health
Time Frame: 6 weeks.

Short Form of 4 questions.

Higher scores mean worse outcomes (score from 1 to 5).

6 weeks.
Adherence to a Mediterranean Diet (PREDIMED questionnaire)
Time Frame: 6 weeks.

Short Form of 4 questions.

Higher scores mean better outcomes (score from 1 to 5).

6 weeks.
International Physical Activity Questionnaire
Time Frame: 6 weeks.

7 questions.

Higher scores mean better outcomes (score from 1 to 5).

6 weeks.
Single-Leg balance
Time Frame: 6 Weeks

Standing in one leg only, be capable of holding the position for 15 seconds. Performed with the dominant leg at first and the non-dominant leg afterwards.

Score from 1 to 15 (higher scores mean better outcomes).

6 Weeks
Upper-Body push strength
Time Frame: 6 Weeks

Number of push-ups in 15 seconds.

The score will be the number of Push-Ups performed (higher scores mean better outcomes).

6 Weeks
Lower-body mechanical power
Time Frame: 6 Weeks

Jump height with countermovement.

The jump will be performed from a standing position, lateral to the wall and jumping to touch the wall as high as possible (with chalk in their finger-prints to mark the height they touched the wall).

The score will be the height of the jump (higher scores mean better outcomes).

6 Weeks
Recovery
Time Frame: 6 Weeks

Static running in 1m2 square as fast as possible for 30 seconds and immediately after, Heart Rate will be monitored for 1 minute

The score will be the difference from the Maximum Heart Rate minus the Heart Rate after 1 minute recovery (higher scores mean better outcomes).

6 Weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Adherence to the treatment (regular training, supplement intake and healthy eating)
Time Frame: 6 weeks
The compliance with the training and supplementation protocols will be measured constantly, as well as the healthy eating patterns. Those participants who have spent 7 days or more in a row without training or taking the supplement, as well as a final accomplishment of the 85% will be discarded from the final analysis.
6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Fernando J Naclerio, Dr, University of Greenwich

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

January 1, 2023

Primary Completion (Anticipated)

May 1, 2023

Study Completion (Anticipated)

May 28, 2023

Study Registration Dates

First Submitted

November 8, 2020

First Submitted That Met QC Criteria

November 13, 2020

First Posted (Actual)

November 16, 2020

Study Record Updates

Last Update Posted (Actual)

December 15, 2021

Last Update Submitted That Met QC Criteria

December 14, 2021

Last Verified

December 1, 2021

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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