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NCT Number: NCT07628764

Within-Individual Variability of Resting Metabolic Rate Over 12 Weeks

This prospective observational study aims to characterize within-individual variability in resting metabolic rate (RMR) over a 12-week period using high-frequency repeated measurements under standardized conditions. Participants will undergo RMR assessments three times per week using whole-room indirect calorimetry.

The study will quantify the magnitude of physiological variability in RMR, distinguish true biological variation from measurement error, and estimate the minimal detectable change required to identify meaningful metabolic adaptations.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

About this study

Resting metabolic rate (RMR) is a major component of total daily energy expenditure and is widely used in metabolic research. However, most studies rely on single or infrequent measurements, assuming RMR is stable within individuals.

Emerging evidence suggests that RMR exhibits measurable within-individual variability, but the temporal structure and magnitude of this variability remain poorly characterized.

This study will implement a high-frequency repeated-measures design, with RMR measured three times per week over 12 weeks using whole-room indirect calorimetry under standardized conditions. This approach will allow detailed characterization of short-term variability and provide estimates for within-subject variability, measurement error, and minimal detectable change.

The findings will inform interpretation of longitudinal metabolic studies and improve study design in future research.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Adults aged 18-65 years
  • Clinically healthy individuals
  • Stable body weight (±2 kg) over the past 3 months
  • Ability and willingness to attend morning measurements three times per week for 12 weeks
  • Ability to provide informed consent

Exclusion criteria

  • Known uncontrolled endocrine or metabolic disease
  • Use of medications known to significantly affect resting metabolic rate (e.g., systemic corticosteroids, unstable thyroid hormone therapy)
  • Acute illness within 14 days prior to enrollment
  • Pregnancy or lactation
  • Any medical condition that, in the opinion of the investigators, may interfere with safe participation

Treatment and study plan

Repeated Measurement of Resting Metabolic Rate

Other

Repeated assessment of resting metabolic rate under standardized conditions; no intervention is administered.

Primary outcomes

  1. Within-Individual Variability in Resting Metabolic Rate (RMR)

    Time frame: 12 weeks

    Within-individual variability in resting metabolic rate (RMR) assessed using repeated measurements under standardized conditions. Variability will be quantified using mean, standard deviation (SD), and coefficient of variation (CV%) across repeated measurements.

Secondary outcomes

  1. Minimal Detectable Change (MDC) in RMR

    Time frame: 12 weeks

    The minimal detectable change in resting metabolic rate required to distinguish true physiological change from measurement variability.

  2. Between-Individual Variability in RMR

    Time frame: 12 weeks

    Assessment of variability in resting metabolic rate between participants based on repeated measurements.

  3. Temporal Trends in RMR

    Time frame: 12 weeks

    Assessment of systematic changes in resting metabolic rate over time using repeated measurements across the study period.

Study contacts

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

Lien Bruck

CONTACT

+972 587487431

Yftach Prof. Gepner

CONTACT

[email protected]

+972 50-682-8501

Sponsors and collaborators

Lead sponsor

Tel Aviv University

Other

Registry information

Official study title

Within-Individual Variability of Resting Metabolic Rate Assessed Repeatedly Over 12 Weeks Using Whole-Room Calorimetry

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jun 5, 2026
Registry last updated
Jun 5, 2026

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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