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NCT Number: NCT06329349

Metabolic Flexibility to Predict Lifestyle Interventions Outcomes

Weight loss is a cornerstone of diabetes (T2D) management, yet in clinical practice, its delivery is limited by its perceived burdensome nature and variability in response. Personalization of the interventions to increase their success rate is an unmet clinical need. The proposed project MEPHISTO (Whole body and gut microbiome metabolic flexibility to predict lifestyle intervention outcomes) would aim to identify predictive features related to successful weight loss upon sequential exercise and diet intervention in people living with obesity. To this end, the study aims to conduct a clinical trial where the investigators would implement state-of-the-art physiological phenotyping of metabolic flexibility at the whole-body level and at the level of the gut in persons with obesity before and after exercise and diet + exercise intervention to identify predictive signatures of successful weight loss

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Key information

Age range

25 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Sports Science, Prague, Czechia

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About this study

Among the influential determinants impacting the efficacy and health outcomes of an intervention is an individual's level of metabolic flexibility (MetFlex). MetFlex denotes the body's capacity to adapt in response to alterations in metabolic demands and nutrient availability. Impaired MetFlex is evident in conditions such as obesity and diabetes, yet it may be ameliorated through lifestyle interventions such as exercise training or caloric restriction similar to improvements in insulin sensitivity. However, MetFlex has not been studied as a potential mechanism associated with successful weight loss. The decline in MetFlex, i.e. the limited cellular/tissue ability to manage excess or deficiency in energy substrates leads to compromised mitochondrial function and excessive lipid accumulation in ectopic tissues, resulting in metabolic disorders such as T2D or metabolic syndrome.

Another potential player predicting an individual's capacity to respond to lifestyle interventions is the gut microbiota (gut microbiome and metabolome, MIME). It was repeatedly shown to be among the most important sources of inter-individual variability when it comes to the development of obesity and responsiveness to dietary intervention The microbiome does not only influence host physiology directly, e.g. through contact with immune cells, but also through the vast array of metabolites produced, i.e. the microbiota-derived metabolome. The composition of the gut microbiota and the microbiota-derived metabolome is largely shaped by the host's diet, as this represents the main source of substances and energy for the microbiota. It is therefore striking that published studies to date have yielded rather inconsistent results regarding dietary interventions to alter gut microbiota composition. The discrepancy can be explained by the large variability of individual microbiomes at the beginning of the intervention, and similarly the baseline MIME signature significantly determines weight loss success.

Here the investigators present a complex project to investigate whether whole body and gut MetFlex can be further explored and used as ex-ante predictors of successful weight loss following exercise and dietary interventions, thus providing proof of concept and paving the way to personalized lifestyle interventions.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BMI>30
  • age 25-45 years

Exclusion criteria

  • active cancer
  • diabetes (medical history, fasting glycemia >7.6 and/or 2hOGTT glycemia >11.1)
  • uncontrolled endocrine diseases
  • corticosteroid therapy
  • immune-suppressive therapy
  • pregnancy
  • breastfeeding

Treatment and study plan

Exercise

Other

12 weeks, 3 times a week of progressive endurance aerobic exercise (150 to 400kcal AEE per session)

Combined Exercise + Diet

Other

12 weeks, 25% caloric reduction, based on PMID: 37069434

Primary outcomes

  1. Change in metabolic flexibility (MetFlex (ΔRQ 200-0))

    Time frame: 18 months

    change in metabolic flexibility measured as ΔRQ (respiratory quotient) during glucose clamp

  2. Change in insulin sensitivity

    Time frame: 18 months

    change in insulin sensitivity measured as glucose infusion rate (GIR) during glucose clamp

Secondary outcomes

  1. Glucose tolerance relate to primary outcomes changes

    Time frame: 18 months

    fasting/2h oral glucose tolerance test glycemia positively relate to weight loss.

  2. HbA1c relate to primary outcomes changes

    Time frame: 18 months

    HbA1c positively relate to weight loss.

  3. Insulin sensitivity relate to primary outcomes changes

    Time frame: 18 months

    GIR positively relate to weight loss.

Other outcomes

  1. Microbiome composition relate to weight loss: exploratory outcome

    Time frame: 18 months

    Change in microbiome composition in fecal samples upon the intervention is a component of successful weight loss and/or metabolic adaptation

  2. Metabolomic signatures relate to weight loss: exploratory outcome

    Time frame: 18 months

    Change in metabolomic signatures in fecal samples upon the intervention is a component of successful weight loss and/or metabolic adaptation

Study contacts

Contact information is provided by the study sponsor or research team.

Jan Gojda, PhD

CONTACT

[email protected]

+420267163031

Jana Potočková

CONTACT

[email protected]

+420267163031

Sponsors and collaborators

Lead sponsor

Charles University, Czech Republic

Other

Collaborators

  • EXCELES LX22NPO5104, CarDia
  • Ministry of Health, Czech Republic

Registry information

Official study title

Whole Body and Gut Microbiome Metabolic Flexibility to Predict Lifestyle Intervention Outcomes

Acronym: MEPHISTO

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Mar 25, 2024
Registry last updated
Aug 28, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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