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Alpha and Omega of Lifestyle Therapy (Alpha&Omega)

8 août 2022 mis à jour par: Inland Norway University of Applied Sciences

Alpha and Omega of Lifestyle Therapy - Resistance Training and Ingestion of n-3 Polyunsaturated Fatty Acids to Improve Health and Muscle Functions in Individuals With Obesity and Healthy Controls

The study aims to investigate the effects of double-blinded, randomized placebo-controlled n3-fatty acid supplementation (1000 mg day-1) and 13 weeks of resistance training on muscle function/biology and systemic health in individuals with obesity (BMI>30) and lean individuals (BMI<30)

Aperçu de l'étude

Description détaillée

Lifestyle therapy is important for treating lifestyle-related morbidities such as obesity. Such therapy often includes exercise and nutrition, and leads to improved health, functionality and quality of life. Unfortunately, obesity leads to adverse changes in the physiological milieu, including inflammation and altered nutritional status such as reduced omega-3:omega-6 ratios. Indeed, inadequate omega 3 levels are common even among lean individuals. This may negatively affect the outcome of lifestyle therapy with exercise, particularly those involving resistance training, contributing to the large heterogeneity seen in training responses. In accordance with this, many individuals (including both lean and obese subjects) fail to improve muscle biology/functions and health, including failure to increase muscle mass and strength, failure to improve glucose handling and inflammatory status. This makes general lifestyle therapy recommendations ineffective. Here, we investigate effects of double-blinded, randomized placebo-controlled n3-fatty acid supplementation (1000 mg day-1) and 13 weeks of low- and high-load resistance training on muscle growth/function/biology and health in individuals with obesity (BMI>30, n=60) and lean controls (BMI<30, n=60). Each participant will perform two different training protocols, one on each leg. The supplement period will commence 7 weeks prior to the onset of the strength training intervention to ensure adequate omega-3 biology at the onset of training. Analyses include assessment of the separate and combined effects of n3-supplementation and obesity on training responses to resistance training, measured as muscle mass, muscle strength/functionality, muscle biological traits, and systemic health variables such as hormone/inflammation/glucose biology, adipose tissue biology/mass, gut microbiome and health-related quality of life. The project will provide important insight into the feasibility of resistance training and n-3 fatty acid supplementation for treating individuals with obesity, paving the way for personalized lifestyle therapy.

The study has two defined main outcome measures, targeting the combined effects of omega-3 and strength training on i) muscle thickness of the thigh (measured using ultrasound; this main outcome measure targets the effects of the intervention on muscle growth), and ii) glucose tolerance (measured using an oral glucose test; this main outcome measure targets the effects of the intervention on improvements in health).

In our analytical approach, we will use a mixed model-approach to assess the main effects of the intervention, mainly defined as changes from before to after the resistance training intervention. Importantly, for health variables such as glucose tolerance, analyses will be performed by accounting for individual variation at baseline, as any beneficial effect can be expected to be higher/present only in individuals with a pathological/diseased starting point. Notably, for many variables, we will collect data from two additional time points (pre-supplementation and after two weeks of familiarization to training). These data will provide insight into additional perspectives, such as the effects of omega-3 intake-only on glucose tolerance, which will bring additional depth to our conclusions (these analyses are not necessarily specified in the Outcome Measures section). For other data, such as primary cultivation of skeletal muscle and muscle mitochondrial respiration, data will only be collected from a randomized subset of participants. For analyses of the effects of the intervention on obesity-related pathophysiologies and health-related quality of life, data from a group of non-intervention individuals will act as reference values (data sampled alongside the intervention). Finally, we will use regression analyses to explain individual differences in training responses, with particular emphasis on muscle hypertrophy/glucose tolerance and their mechanistic origin of nature.

2021/08: The number of anticipated participants was increased from 120 to 150 due to circumstances relating to the SARS-CoV-2 pandemic

Type d'étude

Interventionnel

Inscription (Anticipé)

150

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Lillehammer, Norvège
        • Inland Norway University of Applied Sciences

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

30 ans à 60 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Untrained (less than 2 sessions of resistance exercise per month and less than 3 hours of endurance exercise per week)

Exclusion Criteria:

  • Unstable cardiovascular disease
  • Injuries affecting the ability to perform heavy resistance exercise
  • Mental illness
  • Allergy to local anesthesia
  • Smoking
  • Use of medicine or drugs containing steroids the last two months prior to inclusion

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Science basique
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation factorielle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Aucune intervention: Contrôler
Aucune intervention
Expérimental: Omega 3

Intake of 1 gram omega-3 (capsules) per day for 20 weeks

+ high-load and low-load resistance exercise two times per week for 10 weeks, preceded by 3 weeks of familiarization to training (high-load training)

High-load and low-load resistance exercise two times per week for 10 weeks, preceded by 3 weeks of familiarization to training (high-load training)
1 gram of omega-3 per day for 20 weeks
Autres noms:
  • N-3 PUFA
Comparateur placebo: Placebo

Intake of 1 gram sunflower oleic oil (capsules) per day for 20 weeks

+ high-load and low-load resistance exercise two times per week for 10 weeks, preceded by 3 weeks of familiarization to training (high-load training)

High-load and low-load resistance exercise two times per week for 10 weeks, preceded by 3 weeks of familiarization to training (high-load training)
1 gram of sunflower oleic oil per day for 20 weeks

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Muscle thickness, ultrasound
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Muscle thickness of vastus lateralis and vastus intermedius measured using ultrasound
Changes from before to after the resistance training intervention (week 8 to 20)
Glucose tolerance
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Glucose tolerance measured using an oral glucose tolerance test
Changes from before to after the resistance training intervention (week 8 to 20)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Lean body mass
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Lean body mass measured using whole-body DXA scan
Changes from before to after the resistance training intervention (week 8 to 20)
Fat mass
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Fat mass measured using whole-body DXA scan
Changes from before to after the resistance training intervention (week 8 to 20)
Visceral fat mass
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Visceral fat mass measured using whole-body DXA scan
Changes from before to after the resistance training intervention (week 8 to 20)
Muscle mass, MRI
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Thigh muscle cross sectional area/volume measured using magnetic resonance imaging (MRI)
Changes from before to after the resistance training intervention (week 8 to 20)
Muscle mass, immunohistochemistry
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Fibre type-specific muscle-fibre cross-sectional area measured using immunohistochemistry
Changes from before to after the resistance training intervention (week 8 to 20)
Muscle mass, combined measure
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Muscle mass of the legs measured as the weighted average of data from ultrasound, MRI, immunohistochemistry and DXA measurements
Changes from before to after the resistance training intervention (week 8 to 20)
Muscle fibre type composition
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Muscle fibre type composition measured using immunohistochemistry
Changes from before to after the resistance training intervention (week 8 to 20)
Myonuclear number
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Fiber type-specific myonuclear number measured using immunohistochemistry
Changes from before to after the resistance training intervention (week 8 to 20)
Muscle satellite cell number
Délai: Changes throughout the course of the resistance training intervention (weeks 8, 10 and 20)
Fiber type-specific muscle satellite cell number measured using immunohistochemistry
Changes throughout the course of the resistance training intervention (weeks 8, 10 and 20)
Muscle capillarization
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Fiber type-specific muscle capillarization measured using immunohistochemistry
Changes from before to after the resistance training intervention (week 8 to 20)
Fat infiltration (muscle)
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Fat infiltration in thigh muscle measured using magnetic resonance imaging (MRI)
Changes from before to after the resistance training intervention (week 8 to 20)
Muscle quality
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Muscle strength measured per muscle mass of the legs
Changes from before to after the resistance training intervention (week 8 to 20)
Unilateral lower body maximal strength
Délai: Changes throughout the course of the resistance training intervention (weeks 8, 10 and 20)
The ability of muscles of the lower body to exert maximal force during dynamic movements
Changes throughout the course of the resistance training intervention (weeks 8, 10 and 20)
Unilateral lower body isokinetic muscle strength
Délai: Changes throughout the course of the resistance training intervention (weeks 8, 10 and 20)
The ability of the knee extensors to exert maximal force during isokinetic movements
Changes throughout the course of the resistance training intervention (weeks 8, 10 and 20)
Unilateral lower body isometric muscle strength
Délai: Changes throughout the course of the resistance training intervention (weeks 8, 10 and 20)
The ability of the knee extensors to exert maximal force during isometric actions
Changes throughout the course of the resistance training intervention (weeks 8, 10 and 20)
Peak power output during one-legged cycling
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Maximal cycling performance measured as peak power output (Watt) during an incremental one-legged cycling test
Changes from before to after the resistance training intervention (week 8 to 20)
Oxygen consumption during one-legged cycling
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
The ability to consume oxygen during an incremental one-legged cycling test
Changes from before to after the resistance training intervention (week 8 to 20)
Unilateral lower body muscle endurance
Délai: Changes throughout the course of the resistance training intervention (weeks 8, 10 and 20)
The ability of muscles of the lower body to perform repeated dynamic contractions at a specified submaximal load (70% of 1RM) to exhaustion
Changes throughout the course of the resistance training intervention (weeks 8, 10 and 20)
Waist circumference
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Circumference of the waist measured using measuring tape
Changes from before to after the resistance training intervention (week 8 to 20)
Blood pressure at rest
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Blood pressure at rest measured using an automated upper-arm blood pressure cuff
Changes from before to after the resistance training intervention (week 8 to 20)
Hemoglobin glycosylation (HbA1c)
Délai: Changes throughout the course of the intervention (weeks 0, 8 and 20)
Long-term glucose levels measured as hemoglobin glycosylation of the metabolic syndrome such as waist circumference, blood pressure at rest, lipid profile ( hemoglobin glycosylation (HbA1c) and fasting blood glucose
Changes throughout the course of the intervention (weeks 0, 8 and 20)
Fasting blood glucose
Délai: Changes throughout the course of the intervention (weeks 0, 8 and 20)
Fasting blood glucose measured in serum
Changes throughout the course of the intervention (weeks 0, 8 and 20)
N-3 PUFA (blood)
Délai: Changes throughout the course of the intervention (weeks 0, 8 and 20)
Omega-3 (DHA/EPA) levels in blood
Changes throughout the course of the intervention (weeks 0, 8 and 20)
Inflammatory characteristics of peripheral blood mononuclear cell (PBMC)
Délai: Throughout the course of the intervention (weeks 0, 8 and 20)
Expression of genes associated with inflammation and lipid metabolism in peripheral blood mononuclear cell measured using quantitative PCR
Throughout the course of the intervention (weeks 0, 8 and 20)
Lipid concentrations in blood
Délai: Changes throughout the course of the intervention (weeks 0, 8 and 20)
Concentrations of various lipids and lipid metabolites such as triglycerides, LDL, HDL, ceramides, dihydroceramides, glucosylceramides, and lactosylceramides measured in serum using tageted metabolomics
Changes throughout the course of the intervention (weeks 0, 8 and 20)
Nutritent concentrations in blood
Délai: Changes throughout the course of the intervention (weeks 0, 8 and 20)
Concentrations of nutrients (such as amino acids) and ions (such as iron and calcium) measured in serum
Changes throughout the course of the intervention (weeks 0, 8 and 20)
Hormone concentrations in blood
Délai: Changes throughout the course of the intervention (weeks 0, 8 and 20)
Concentrations of hormones such as testosterone, growth hormone, thyroid hormones, cortisol and insulin (as well as c-peptide) measured in serum
Changes throughout the course of the intervention (weeks 0, 8 and 20)
Concentrations of inflammatory factors in blood
Délai: Changes throughout the course of the intervention (weeks 0, 8 and 20)
Levels of inflammatory factors such as IL6, CRP and NFkB in serum
Changes throughout the course of the intervention (weeks 0, 8 and 20)
Muscle fractional synthesis rate
Délai: Week 18 to 20
Protein/RNA synthesis rate measured using heavy water (deuterium) and chromatography/spectrometry
Week 18 to 20
Gene expression in skeletal muscle (intervention)
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
RNA (e.g. messenger RNA, ribosomal RNA, microRNA, long non-coding RNA) abundances in m. vastus lateralis, measured both as targeted genes and at the level of the transcriptome
Changes from before to after the resistance training intervention (week 8 to 20)
Gene expression in skeletal muscle (familiarization)
Délai: Changes from before to after familiarization to resistance exercise (week 8 to 10)
RNA (e.g. messenger RNA, ribosomal RNA, microRNA, long non-coding RNA) abundances in m. vastus lateralis, measured both as single genes and at the level of the transcriptome
Changes from before to after familiarization to resistance exercise (week 8 to 10)
Protein abundance in skeletal muscle (intervention)
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Levels of proteins and their modification status (e.g. phosphorylation) in m. vastus lateralis, measured at the level of single proteins and at the level of the proteome
Changes from before to after the resistance training intervention (week 8 to 20)
Protein abundance in skeletal muscle (familiarization)
Délai: Changes from before to after the resistance training intervention (week 8 to 10)
Levels of proteins and their modification status (e.g. phosphorylation) in m. vastus lateralis, measured at the level of single proteins and at the level of the proteome
Changes from before to after the resistance training intervention (week 8 to 10)
Mitochondrial functions in muscle
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
The ability of muscle mitochondria (extracted from muscle homogenate) to synthesize ATP in vitro
Changes from before to after the resistance training intervention (week 8 to 20)
Gene expression in subcutaneous fat
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
RNA (e.g. messenger RNA, ribosomal RNA, microRNA, long non-coding RNA) abundances in subcutaneous fat, measured as targeted genes
Changes from before to after the resistance training intervention (week 8 to 20)
Satellite cell proliferation and myotube growth (in vitro)
Délai: Changes from before to after N3-supplementation-only (week 0 to 8)
The ability of muscle satellite cells (extracted from muscle homogenate) to proliferate (rates of cell division), differentiate into myotubes and subsequently grow (rates of change in myotube size) in primary cultures
Changes from before to after N3-supplementation-only (week 0 to 8)
Musculoskeletal pain (Nordic Pain Questionnaire)
Délai: Changes throughout the course of the training intervention (weeks 0, 8 and 20)
Musculoskeletal pain measured using The standardized Nordic Pain Questionnaire
Changes throughout the course of the training intervention (weeks 0, 8 and 20)
Musculoskeletal pain (VAS)
Délai: Changes throughout the course of the training intervention (weeks 0, 8 and 20)
Musculoskeletal pain measured using VAS-scale (1-10)
Changes throughout the course of the training intervention (weeks 0, 8 and 20)
Gastrointestinal symptoms
Délai: Changes throughout the course of the training intervention (weeks 0, 8 and 20)
Gastrointestinal symptoms such as abdominal discomfort and pain, measured using Rome IV criteria
Changes throughout the course of the training intervention (weeks 0, 8 and 20)
Gut microbiome (feces, N3-supplementation-only)
Délai: Changes from before to after N3-supplementation-only (week 0 to 8)
Relative composition of the gut microbiome measured using quantitative polymerase chain reaction
Changes from before to after N3-supplementation-only (week 0 to 8)
Gut microbiome (feces, training intervention)
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Relative composition of the gut microbiome measured using quantitative polymerase chain reaction
Changes from before to after the resistance training intervention (week 8 to 20)
Fecal short-chained fatty acids (N3-supplementation-only)
Délai: Changes from before to after N3-supplementation-only (week 0 to 8)
Short chained fatty acids measured in feces
Changes from before to after N3-supplementation-only (week 0 to 8)
Fecal short-chained fatty acids (training intervention)
Délai: Changes from before to after the resistance training intervention (week 8 to 20)
Short chained fatty acids measured in feces
Changes from before to after the resistance training intervention (week 8 to 20)
Arterial stiffness
Délai: Throughout the course of the intervention (week 0, 8 and 20)
Arterial stiffness measured using pulse-wave velocity
Throughout the course of the intervention (week 0, 8 and 20)
Health-related quality of life (SF-36)
Délai: Changes throughout the course of the intervention (week 0, 8 and 20)
Health-related quality of life measured using the SF-36 questionnaire
Changes throughout the course of the intervention (week 0, 8 and 20)
Health-related quality of life in overweight/obesity
Délai: Changes throughout the course of the intervention (week 0, 8 and 20)
Health-related quality of life in overweight/obesity individuals measured using The impact of weight on quality of life (IWQOL) questionnaire
Changes throughout the course of the intervention (week 0, 8 and 20)
Health-related quality of life (PANAS)
Délai: Changes throughout the course of the intervention (week 0, 8 and 20)
Health-related quality of life measured using the Positive and Negative Affect Schedule (PANAS) questionnaire
Changes throughout the course of the intervention (week 0, 8 and 20)
Activities of daily living
Délai: Changes throughout the course of the intervention (week 0, 8 and 20)
Activities of daily living (e.g. time spent in physical activity, intensities of activities) measured using questionnaire
Changes throughout the course of the intervention (week 0, 8 and 20)

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Training diary relating to the intervention protocol
Délai: Weeks 8 to 20
Information about intervention-specific training, including training frequency, volume and load
Weeks 8 to 20
Dietary registration
Délai: Week 0, 8 and 20
Dietary registration measured using a food frequency questionnaire, assessing nutritional composition, energy intake and habitual patterns of dietary intake
Week 0, 8 and 20

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Stian Ellefsen, PhD, Inland Norway University of Applied Sciences

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

2 septembre 2019

Achèvement primaire (Réel)

30 mars 2022

Achèvement de l'étude (Anticipé)

1 décembre 2026

Dates d'inscription aux études

Première soumission

19 janvier 2020

Première soumission répondant aux critères de contrôle qualité

19 février 2020

Première publication (Réel)

21 février 2020

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

9 août 2022

Dernière mise à jour soumise répondant aux critères de contrôle qualité

8 août 2022

Dernière vérification

1 août 2022

Plus d'information

Termes liés à cette étude

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • Trainome 2019#015

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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