Effects of Intermittent Versus Continuous Energy Restriction on Metabolic Adaptation in Women With Obesity (BREAK)
Primary Purpose
Obesity, Weight Loss
Status
Active
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Intermittent energy restriction (IER)
Continuous energy restriction (CER)
Sponsored by
About this trial
This is an interventional treatment trial for Obesity focused on measuring Adaptive Thermogenesis, Metabolic Slowing
Eligibility Criteria
Inclusion Criteria:
- Women
- BMI ranging between 30 and 39.9 kg/m2
- Age between 20-45 years
- Weight stable in the last 6 months (less than 5% weigh variation)
- Inactive (less then 150 min/week of moderate physical activity or 75 min/week of vigorous physical activity
- Living in Lisbon Metropolitan Area and being able to drive to Faculty of Human Kinetics and Germano de Sousa Laboratory (Algés)
- Available to be randomized to any of the trial groups (CER or IER)
- Willing to commit with the assigned group protocol, including the nutritional intervention and lifestyle recommendations, as well as being available for participation in all evaluation moments.
Exclusion Criteria:
- Previous or present health disorders: cancer, autoimmune, cardiac, psychiatric, kidney and liver disease (except liver steatosis), diabetes, chronic intestinal inflammatory disease, or other medical conditions known to affect energy balance homeostasis
- Menopause
- Hormonal or thyroid disorder
- Medications that promote weight gain or alter energy balance, including corticosteroids, antidepressants, anxiolytics, mood-stabilizing, and antipsychotics
- Medications or dietary supplements for weight-loss in the past 3 months
- Pregnant for the past 6 months or breastfeeding
- Planning to get pregnant in the next 2 years or getting pregnant during the study
- Current consumption of more than 14 alcoholic drinks per week or other substance abuse, and/or current acute treatment or rehabilitation program for alcohol/substance abuse
- Surgery or in hospital admission for the last month
- Positive for Covid-19 in the past 3 months or testing positive during the intervention phase of the study
Sites / Locations
- Faculdade de Motricidade Humana da Universidade de Lisboa
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Intermittent energy restriction (IER)
Continuous energy restriction (CER)
Arm Description
Initially participants will undergo 2-weeks of neutral energy balance (EB). After this, the IER will consist of: 2-weeks of energy restriction interspersed with 1-week in neutral EB (total of 23-week period). At the end, 8-weeks in neutral EB will be required.
Similarly to IER, CER participants will undergo 2-weeks of neutral EB. After this, the CER will consist of: 16-weeks of continuous energy restriction. At the end, 8-weeks in neutral EB will be required.
Outcomes
Primary Outcome Measures
Fat mass
To estimate total fat mass (FM), dual energy X-ray absorptiometry (Hologic Explorer-W, Waltham, USA) will be used. A whole-body scan will be performed and the attenuation of X-rays pulsed between 70 and 140 kV synchronously with the line frequency for each pixel of the scanned image will be measured.
Adaptive thermogenesis (AT)
AT will be assessed as: AT (kcal/d) = (pREE at the end of the intervention - mREE at the end of the intervention) - (pREE baseline - mREE baseline)
Secondary Outcome Measures
Weight
Weight will be determined using a digital scale, with 0,1 kg interval (Seca, Hamburg, Germany).
Height
Height will be determined using a stadiometer Seca 704 s, with 0,1 cm intervals (Seca, Hamburg, Germany)
Body mass index (BMI)
BMI will be calculated using the formula [weight (kg)/height2(m2)]
Fat-free mass (FFM)
To estimate fat-free mass (FFM), dual energy X-ray absorptiometry (Hologic Explorer-W, Waltham, USA) will be used. A whole-body scan will be performed and the attenuation of X-rays pulsed between 70 and 140 kV synchronously with the line frequency for each pixel of the scanned image will be measured.
Resting energy expenditure (REE)
REE will be determined using indirect calorimetry COSMED Fitmate device (Cosmed, Rome, Italy) will be used to measure breath-by-breath oxygen consumption (V̇O2 ) and carbon dioxide production (V̇CO2) using a facial mask.
Energy balance (EB)
The EB will be calculated as: EB (kcal/d) = 1.0 * (ΔFMM/Δt) + 9.5 * (ΔFM/Δt). ΔFM and ΔFFM represent the change in grams of FM and FFM from the beginning to end of the intervention and Δt is the time length of the intervention in days.
Free-living physical activity
The amount of activity assessed by the Actigraph accelerometer will be expressed as minutes per day spent in different intensities. The cutoff values used to define the intensity of PA and therefore to quantify the mean time in each intensity (sedentary, light, moderate or vigorous) will be: sedentary: < 100 counts·min-1; light: 100-2019 counts·min-1; moderate: 2020-5998 counts·min-1 (corresponding to 3-5.9 METs); vigorous: ≥ 5999 counts·min-1 (corresponding to ≥6 METs). A valid day will be defined as having 600 or more minutes (≥10h) of monitor wear during waking hours.
Total daily energy expenditure (TDEE)
TDEE will be assessed by the Actigraph accelerometer using the Crouter et al equations.
Physical activity energy expenditure (PAEE)
PAEE will be calculated as total energy expenditure (TEE) minus (0.1*TEE + REE), assuming the thermic effect of food represents 10% of TEE, and REE represents Resting energy expenditure.
Blood thyroid levels
Free T3 and free T4 will be run by immunoassay with chemiluminescent detection (Advia Centaur, Siemens).
Blood insulin levels
Blood insulin levels assessment will be performed in an automated analyser with chemiluminescent detection [Advia Centaur, Siemens].
Blood leptin levels
Serum levels of leptin will be measured by enzyme immunoassay [ELISA].
Blood cortisol levels
Blood levels of cortisol will be determined by immunoassay with chemiluminescence detection [Advia Centaur, Siemens].
Full Information
NCT ID
NCT05184361
First Posted
December 17, 2021
Last Updated
November 8, 2022
Sponsor
Universidade do Porto
Collaborators
University of Lisbon
1. Study Identification
Unique Protocol Identification Number
NCT05184361
Brief Title
Effects of Intermittent Versus Continuous Energy Restriction on Metabolic Adaptation in Women With Obesity
Acronym
BREAK
Official Title
Effects of Intermittent Versus Continuous Energy Restriction on Metabolic Adaptation in Women With Obesity
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 13, 2022 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
January 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universidade do Porto
Collaborators
University of Lisbon
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
One of the major challenges for treating obesity is to maintain a weight reduced state on the long term due to the high rate of weight regain. Therefore, the aim of this study is to evaluate the effects of an intermittent versus a continuous energy restriction in body composition (body weight, fat mass and fat-free mass) and metabolic adaptation, in women with obesity.
Detailed Description
Literature is full of lifestyle interventions aimed for weight loss (WL) in several populations. However, one of the major challenges for treating obesity is WL maintenance on the long term due to the high rate of weight regain.
The reduction of the resting metabolic rate (RMR) is one of the identified aspects regarding compensatory metabolic alterations. After a WL intervention, decreases in RMR are mainly explained by the loss of fat-mass (FM) and fat-free mass (FFM). However, some authors showed that these reductions tend to be higher than predicted (explained by FM and FFM loss), a phenomenon called "metabolic adaptation" (MA). MA has been studied as a possible barrier to WL, WL maintenance and may contribute to weight regain. However, its relevance on long-term WM has been recently questioned. It is known that in order to lose weight, a negative energy balance (EB) must be achieved, meaning when EE surpasses the energy intake (EI). However, this negative EB may be achieved through several strategies, by changing the EI (energy restriction (ER)) and/or EE (increasing physical activity).
Regarding EI strategies, continuous energy restriction (CER) is the most common nutritional strategy for WL, consisting in a daily energy restriction according to one's specific needs. However, some concern has been pointed out regarding this widely used strategy, once it evolves several behavioural, metabolic and endocrine responses that may contribute to therapeutic adherence, undermining WL and its maintenance. On the other hand, intermittent energy restriction (IER) has been recently suggested as an alternative to CER. IER consists in interspersing periods of ER with periods of neutral EB, called "refeed" or "diet breaks" during the WL phase. Energy restriction is followed by several adaptive responses, namely endocrine, including thyroid, appetite regulation and steroid hormones, influencing the energy expenditure (EE), body composition and satiety. Therefore, understanding how hormones may influence RMR and as a consequence, AT, it´s crucial to a better understanding.
According to the literature, compensatory metabolic responses following ER and WL can be reversed following a 7-to-14-day period of energy balance post-weight loss. Therefore, considering that the length of the nutritional intervention for WL may benefit a reduction, we consider relevant to study other ER designs/patterns, namely 2 weeks in ER interspersed with 1 week in EB, comparing to a CER. Taking into account this therapeutic as a potential opportunity for the obesity's treatment, this paper describes the protocol for a randomized controlled trial (RCT), which targets to evaluate the effects of an IER (alternating 2 weeks of ER with 1 in neutral EB), comparing to a CER. This trial aims: a) to compare the effects of a IER vs CER strategy on body composition variables (body weight, fat mass and fat-free mass) and in metabolic adaptation and, b) to understand if participants will be able to maintain a reduced weight state after 12 months (successful weight-loss maintenance), in both groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Weight Loss
Keywords
Adaptive Thermogenesis, Metabolic Slowing
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
74 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intermittent energy restriction (IER)
Arm Type
Experimental
Arm Description
Initially participants will undergo 2-weeks of neutral energy balance (EB). After this, the IER will consist of: 2-weeks of energy restriction interspersed with 1-week in neutral EB (total of 23-week period).
At the end, 8-weeks in neutral EB will be required.
Arm Title
Continuous energy restriction (CER)
Arm Type
Active Comparator
Arm Description
Similarly to IER, CER participants will undergo 2-weeks of neutral EB. After this, the CER will consist of: 16-weeks of continuous energy restriction. At the end, 8-weeks in neutral EB will be required.
Intervention Type
Behavioral
Intervention Name(s)
Intermittent energy restriction (IER)
Intervention Description
Both groups will be accompanied by a registered dietitian in order to provide an individual and personalized diet plan that will suppress the respective daily requirements for each phase. Macronutrient distribution will be the following: 35% protein, 35% carbohydrate and 30% fat.
Daily energy requirements (DER) will be calculated by multiplying measured RMR (through indirect calorimetry) by physical activity level (PAL), assessed by accelerometry.
In order to achieve a neutral EB, 100% of their daily energy requirements (DER) will be prescribed for each participant. For both groups, an energy restriction of 33% of one's DER will be created. The IER group will alternate between 2-weeks in energy restriction (67% DER) and 1-week in neutral EB (100% DER), in a total of 23-weeks.
The IER group will alternate between 2-weeks in energy restriction (67% DER) and 1-week in neutral EB (100% DER), in a total of 23-weeks.
Intervention Type
Behavioral
Intervention Name(s)
Continuous energy restriction (CER)
Intervention Description
A dietary plan comprising 67% of DER will be prescribed to the CER group. Participants will be asked to follow this plan in a total of 16-weeks, without interruptions.
Primary Outcome Measure Information:
Title
Fat mass
Description
To estimate total fat mass (FM), dual energy X-ray absorptiometry (Hologic Explorer-W, Waltham, USA) will be used. A whole-body scan will be performed and the attenuation of X-rays pulsed between 70 and 140 kV synchronously with the line frequency for each pixel of the scanned image will be measured.
Time Frame
24 months
Title
Adaptive thermogenesis (AT)
Description
AT will be assessed as: AT (kcal/d) = (pREE at the end of the intervention - mREE at the end of the intervention) - (pREE baseline - mREE baseline)
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Weight
Description
Weight will be determined using a digital scale, with 0,1 kg interval (Seca, Hamburg, Germany).
Time Frame
24 months
Title
Height
Description
Height will be determined using a stadiometer Seca 704 s, with 0,1 cm intervals (Seca, Hamburg, Germany)
Time Frame
Baseline
Title
Body mass index (BMI)
Description
BMI will be calculated using the formula [weight (kg)/height2(m2)]
Time Frame
24 months
Title
Fat-free mass (FFM)
Description
To estimate fat-free mass (FFM), dual energy X-ray absorptiometry (Hologic Explorer-W, Waltham, USA) will be used. A whole-body scan will be performed and the attenuation of X-rays pulsed between 70 and 140 kV synchronously with the line frequency for each pixel of the scanned image will be measured.
Time Frame
24 months
Title
Resting energy expenditure (REE)
Description
REE will be determined using indirect calorimetry COSMED Fitmate device (Cosmed, Rome, Italy) will be used to measure breath-by-breath oxygen consumption (V̇O2 ) and carbon dioxide production (V̇CO2) using a facial mask.
Time Frame
24 months
Title
Energy balance (EB)
Description
The EB will be calculated as: EB (kcal/d) = 1.0 * (ΔFMM/Δt) + 9.5 * (ΔFM/Δt). ΔFM and ΔFFM represent the change in grams of FM and FFM from the beginning to end of the intervention and Δt is the time length of the intervention in days.
Time Frame
24 months
Title
Free-living physical activity
Description
The amount of activity assessed by the Actigraph accelerometer will be expressed as minutes per day spent in different intensities. The cutoff values used to define the intensity of PA and therefore to quantify the mean time in each intensity (sedentary, light, moderate or vigorous) will be: sedentary: < 100 counts·min-1; light: 100-2019 counts·min-1; moderate: 2020-5998 counts·min-1 (corresponding to 3-5.9 METs); vigorous: ≥ 5999 counts·min-1 (corresponding to ≥6 METs). A valid day will be defined as having 600 or more minutes (≥10h) of monitor wear during waking hours.
Time Frame
24 months
Title
Total daily energy expenditure (TDEE)
Description
TDEE will be assessed by the Actigraph accelerometer using the Crouter et al equations.
Time Frame
24 months
Title
Physical activity energy expenditure (PAEE)
Description
PAEE will be calculated as total energy expenditure (TEE) minus (0.1*TEE + REE), assuming the thermic effect of food represents 10% of TEE, and REE represents Resting energy expenditure.
Time Frame
24 months
Title
Blood thyroid levels
Description
Free T3 and free T4 will be run by immunoassay with chemiluminescent detection (Advia Centaur, Siemens).
Time Frame
24 months
Title
Blood insulin levels
Description
Blood insulin levels assessment will be performed in an automated analyser with chemiluminescent detection [Advia Centaur, Siemens].
Time Frame
24 months
Title
Blood leptin levels
Description
Serum levels of leptin will be measured by enzyme immunoassay [ELISA].
Time Frame
24 months
Title
Blood cortisol levels
Description
Blood levels of cortisol will be determined by immunoassay with chemiluminescence detection [Advia Centaur, Siemens].
Time Frame
24 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Women
BMI ranging between 30 and 39.9 kg/m2
Age between 20-45 years
Weight stable in the last 6 months (less than 5% weigh variation)
Inactive (less then 150 min/week of moderate physical activity or 75 min/week of vigorous physical activity
Living in Lisbon Metropolitan Area and being able to drive to Faculty of Human Kinetics and Germano de Sousa Laboratory (Algés)
Available to be randomized to any of the trial groups (CER or IER)
Willing to commit with the assigned group protocol, including the nutritional intervention and lifestyle recommendations, as well as being available for participation in all evaluation moments.
Exclusion Criteria:
Previous or present health disorders: cancer, autoimmune, cardiac, psychiatric, kidney and liver disease (except liver steatosis), diabetes, chronic intestinal inflammatory disease, or other medical conditions known to affect energy balance homeostasis
Menopause
Hormonal or thyroid disorder
Medications that promote weight gain or alter energy balance, including corticosteroids, antidepressants, anxiolytics, mood-stabilizing, and antipsychotics
Medications or dietary supplements for weight-loss in the past 3 months
Pregnant for the past 6 months or breastfeeding
Planning to get pregnant in the next 2 years or getting pregnant during the study
Current consumption of more than 14 alcoholic drinks per week or other substance abuse, and/or current acute treatment or rehabilitation program for alcohol/substance abuse
Surgery or in hospital admission for the last month
Positive for Covid-19 in the past 3 months or testing positive during the intervention phase of the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vítor H Teixeira, PhD
Organizational Affiliation
Faculty of Nutrition and Food Sciences, University of Porto
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Analiza M Silva, PhD
Organizational Affiliation
Faculty of Human Kinetics, University of Lisbon
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculdade de Motricidade Humana da Universidade de Lisboa
City
Cruz Quebrada
State/Province
Lisbon
ZIP/Postal Code
1495-751
Country
Portugal
12. IPD Sharing Statement
Plan to Share IPD
No
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Effects of Intermittent Versus Continuous Energy Restriction on Metabolic Adaptation in Women With Obesity
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