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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)

14. Dezember 2021 aktualisiert von: 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.

Studienübersicht

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Voraussichtlich)

3000

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

  • Name: Joel Puente Fernández, PhD Student
  • Telefonnummer: +34626610821
  • E-Mail: jp2979a@gre.ac.uk

Studieren Sie die Kontaktsicherung

Studienorte

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

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

40 Jahre bis 70 Jahre (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Alle

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Verdreifachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
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.
Andere Namen:
  • Preworkout
The information about it has been detailed in advance.
Andere Namen:
  • RT
  • PRT
This intervention has also been described in advance.
Andere Namen:
  • Ernährung
  • Gesunde Ernährung
Aktiver Komparator: 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.
Andere Namen:
  • RT
  • PRT
This intervention has also been described in advance.
Andere Namen:
  • Ernährung
  • Gesunde Ernährung
Schein-Komparator: 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.
Andere Namen:
  • RT
  • PRT
This intervention has also been described in advance.
Andere Namen:
  • Ernährung
  • Gesunde Ernährung

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Fat Mass
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 6 weeks.

Short Form of 12 questions.

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

6 weeks.
Pittsburgh Sleep Quality Index
Zeitfenster: 6 weeks.

Short Form of 4 questions.

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

6 weeks.
Stress Level and Mental Health
Zeitfenster: 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)
Zeitfenster: 6 weeks.

Short Form of 4 questions.

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

6 weeks.
International Physical Activity Questionnaire
Zeitfenster: 6 weeks.

7 questions.

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

6 weeks.
Single-Leg balance
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Adherence to the treatment (regular training, supplement intake and healthy eating)
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Studienleiter: Fernando J Naclerio, Dr, University of Greenwich

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Voraussichtlich)

1. Januar 2023

Primärer Abschluss (Voraussichtlich)

1. Mai 2023

Studienabschluss (Voraussichtlich)

28. Mai 2023

Studienanmeldedaten

Zuerst eingereicht

8. November 2020

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

13. November 2020

Zuerst gepostet (Tatsächlich)

16. November 2020

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

15. Dezember 2021

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

14. Dezember 2021

Zuletzt verifiziert

1. Dezember 2021

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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