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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)

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)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04630977
Enrollment
3000
Registered
2020-11-16
Start date
2023-01-01
Completion date
2023-05-28
Last updated
2021-12-15

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

Conditions

Happiness, Muscle Loss, Obesity, Obesity, Abdominal, Quality of Life, Self-Perception, Stress, Psychological, Weight Loss

Keywords

Weight Loss, Body Composition, Home-Based, Supplement, Multi-ingredient

Brief summary

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.

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.

Interventions

DIETARY_SUPPLEMENTMulti-ingredient Pre-workout supplement

Every important issue has been detailed before.

OTHERProgressive Resistance Training

The information about it has been detailed in advance.

BEHAVIORALNutritional Patterns Guideline

This intervention has also been described in advance.

Sponsors

Ingesport Health Spa Consulting
CollaboratorUNKNOWN
University of Greenwich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

Every participant will be randomized to any of the groups. The principal investigator will be blinded for the supplement and allocation of the participants until the end of the analysis of the results after the intervention. Therefore, an external and third researcher will send the supplements to every participant and will keep the record of the randomised allocation of each of them until the end of the analysis of the last outcomes assessments collection.

Intervention model description

One group will intake a pre-workout multi-ingredient supplement. The second group will intake an isocaloric placebo containing only carbohydrates. The third group (control) will take a non-caloric placebo.

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Recovery6 WeeksStatic 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).
Pittsburgh Sleep Quality Index6 weeks.Short Form of 4 questions. Higher scores mean better outcomes (score from 1 to 5).
Stress Level and Mental Health6 weeks.Short Form of 4 questions. Higher scores mean worse outcomes (score from 1 to 5).
Fat MassThrough study completion, an average of 1 year.Assessment of the total adipose tissue via Bioelectrical Impedance.
Fat-free MassThrough study completion, an average of 1 year.Assessment of the total lean mass via Bioelectrical Impedance.
Health Perception questionnaire6 weeks.Short Form of 12 questions. Higher scores mean better outcomes (score from 0 to 100).
Adherence to a Mediterranean Diet (PREDIMED questionnaire)6 weeks.Short Form of 4 questions. Higher scores mean better outcomes (score from 1 to 5).
International Physical Activity Questionnaire6 weeks.7 questions. Higher scores mean better outcomes (score from 1 to 5).
Single-Leg balance6 WeeksStanding 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).
Upper-Body push strength6 WeeksNumber of push-ups in 15 seconds. The score will be the number of Push-Ups performed (higher scores mean better outcomes).
Lower-body mechanical power6 WeeksJump 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).

Secondary

MeasureTime frameDescription
Adherence to the treatment (regular training, supplement intake and healthy eating)6 weeksThe 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.

Countries

United Kingdom

Contacts

Primary ContactJoel Puente Fernández, PhD Student
jp2979a@gre.ac.uk+34626610821
Backup ContactFernando J Naclerio, Dr
F.J.Naclerio@greenwich.ac.uk+44 (0)20 8331 8441

Outcome results

None listed

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