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Study of Eating Patterns With a Smartphone App and the Effects of Time Restricted Feeding in the Metabolic Syndrome

Primary Purpose

Eating Behavior, Metabolic Syndrome, Obesity

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Time restricted feeding
Regular dietary advices
Eating patterns
Sponsored by
University of Lausanne Hospitals
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Eating Behavior focused on measuring Time Restricted Feeding, Eating patterns

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Key inclusion criteria for both observation and intervention phases (Part 1+2):

  • Age ≥ 12 years
  • Body mass index ≥ 20 kg/m2 and stable weight (previous 3 months) in adults; BMI ≥ 25th percentile in teenagers
  • Smartphone compatible with the app (iOS or Android systems)

Additional inclusion criteria for the intervention phase (Part 2):

  • Any component of the metabolic syndrome following the International Diabetes Federation consensus definition
  • Eating duration >14h during the observation phase

Additional inclusion criteria for the mechanistic study (Part 3):

  • Age 18-40 years, men and pre-menopausal women
  • BMI 30-40 kg/m2
  • In the fasting state (at least 8 hours)

Key exclusion criteria for both observation and intervention phases (Part 1+2):

  • Pregnant and breastfeeding women, plans for maternity during the study
  • Major illness/fever over the previous month, active cancer
  • Eating disorder, on a diet / weight management, prior bariatric surgery
  • Major mental illness, unable to give informed consent
  • Current shift work or travel abroad planned in the next month

Additional exclusion criteria for the intervention phase (Part 2):

  • Prior cardiovascular event
  • Major liver, gastrointestinal, renal or endocrine disorder, diabetes mellitus with hypoglycemic drug(s)
  • Major sleep disorder, centrally acting medication
  • Lipid lowering drug, hypoglycemic drug, medication affecting the gut

Additional exclusion criteria for the mechanistic study (Part 3):

  • Impaired glucose tolerance (pre-diabetes) or diabetes mellitus
  • Positive pregnancy test

Sites / Locations

  • Inselspital, Klinik für Allgemeine Innere Medizin
  • University Hospital of Lausanne (CHUV)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Time restricted feeding

Regular dietary advices

Arm Description

For those in the intervention phase (Part 2)

For those in the intervention phase (Part 2)

Outcomes

Primary Outcome Measures

Eating duration
Duration from the first to last caloric intake over 24-hour cycle, collected via the smartphone app. Note: Key inclusion criterion for the intervention phase (Part 2).
Change of metabolic syndrome components
Number of participants with changes in weight and/or lipid profile and/or glucose metabolism in the intervention phase (Part 2). Note: Changes of the different components will be analyzed separately as secondary outcomes.

Secondary Outcome Measures

Adherence to TRF intervention
After allocation to the TRF arm, assessment of the adherence to the intervention, as measured by eating duration from the first to last caloric intake over 24-hour cycle.
Weight change
Part of the composite primary outcome in the intervention phase (Part 2)
Change in lipid profile
Part of the composite primary outcome in the intervention phase (Part 2)
Change in glucose metabolism
Part of the composite primary outcome in the intervention phase (Part 2)
Change in blood pressure
Systolic and diastolic blood pressure
Change in hepatic steatosis / fibrosis score
As measured by the Fibroscan device
Change in number of meals per day
Temporal analysis of caloric intake events collected by the smartphone app
Change in meal intervals
Temporal analysis of caloric intake events collected by the smartphone app
Change in fraction of calories consumed after noon
Estimation of caloric content from food pictures collected by the smartphone app
Change in fraction of calories consumed after 6pm
Estimation of caloric content from food pictures collected by the smartphone app
Change in eating pattern difference between weekdays and weekends
Indirect assessment of different lifestyle habits during weekdays and weekends

Full Information

First Posted
April 2, 2017
Last Updated
October 20, 2022
Sponsor
University of Lausanne Hospitals
Collaborators
Salk Institute for Biological Studies
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1. Study Identification

Unique Protocol Identification Number
NCT03241121
Brief Title
Study of Eating Patterns With a Smartphone App and the Effects of Time Restricted Feeding in the Metabolic Syndrome
Official Title
Study of Eating Patterns With a Smartphone App and the Metabolic Effects of Time Restricted Feeding (TRF) in the Metabolic Syndrome - An Open-label Randomized Controlled Trial of TRF vs Regular Dietary Advices
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
September 29, 2017 (Actual)
Primary Completion Date
March 31, 2021 (Actual)
Study Completion Date
March 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Lausanne Hospitals
Collaborators
Salk Institute for Biological Studies

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
SwissChronoFood - Study of eating patterns with a smartphone app and the metabolic effects of time restricted feeding in metabolic syndrome The purpose of this study is to assess eating patterns among teenagers and adults with a new method, going beyond the pen-and-paper food diaries, and to investigate whether time restricted feeding leads to weight loss, improvement in lipid and glucose metabolism in individuals with components of the metabolic syndrome
Detailed Description
The prevalence of the metabolic syndrome (MS) is increasing worldwide, due to the progression of its different components (central obesity, elevated blood pressure, impaired glucose tolerance and dyslipidemia), as well as the often associated liver steatosis. One way to tackle the obesity epidemic is to intervene early at the onset in childhood and teenage years - before cardio-metabolic complications have occurred. However, lifestyle programs targeting this age group had limited success in the current obesogenic environment. In particular, weight loss is a key factor in controlling all MS components, yet it is difficult to maintain over time. Time restricted feeding (TRF) is an approach that emphasizes energy intake limited to certain windows of time within the 24-hour cycle without restrictions on calories or macronutrients. This has emerged as an appealing approach to reduce body weight while improving lipid profile and glucose metabolism. However, TRF has been mostly studied in animals and long-term prospective data on its efficacy and mechanisms in humans is lacking. Prior to the intervention, the investigators will assess the eating patterns of participants with an innovative smartphone application ('app') which is less intrusive and more reliable than food diaries/questionnaires to assess eating behavior and patterns. In this project, the investigators will assess eating patterns among teenagers and adults, and investigate whether a controlled TRF intervention leads to beneficial changes in MS components. Study Part 1 uses an epidemiological approach to establish baseline daily eating behavior, physical activity patterns and sleeping habits over 2 weeks (teenagers) and 4 weeks (adults) using the smartphone app. Those individuals meeting criteria for at least one component of MS and who have eaten for >14 hours per 24-hour cycle will be recruited for Study Part 2. In Part 2, participants will be assigned to TRF or active control groups, and followed in this pragmatic randomized controlled trial for 6 weeks (teenagers) and 6 months (adults) to assess the change in their weight and MS components, as well as liver fat deposits. Study Part 3 will investigate the underlying mechanisms of improved metabolic profile with TRF.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eating Behavior, Metabolic Syndrome, Obesity, Dyslipidemias, Glucose Intolerance, Steatosis of Liver
Keywords
Time Restricted Feeding, Eating patterns

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Study Part 1: Prospective longitudinal observational study. Study Part 2/3: Open-label randomized controlled trial.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
235 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Time restricted feeding
Arm Type
Experimental
Arm Description
For those in the intervention phase (Part 2)
Arm Title
Regular dietary advices
Arm Type
Active Comparator
Arm Description
For those in the intervention phase (Part 2)
Intervention Type
Behavioral
Intervention Name(s)
Time restricted feeding
Intervention Description
To eat only during a self-selected window of 12 hours, with no advice on nutrition quality, quantity or caloric intake
Intervention Type
Behavioral
Intervention Name(s)
Regular dietary advices
Intervention Description
Regular dietary advices by a trained dietitian or research nurse according to current nutrition guidelines
Intervention Type
Device
Intervention Name(s)
Eating patterns
Intervention Description
Data collection on eating patterns via the smartphone app
Primary Outcome Measure Information:
Title
Eating duration
Description
Duration from the first to last caloric intake over 24-hour cycle, collected via the smartphone app. Note: Key inclusion criterion for the intervention phase (Part 2).
Time Frame
From baseline visit to end of observation phase (Part 1: 4 weeks for adults, 2 weeks for teenagers)
Title
Change of metabolic syndrome components
Description
Number of participants with changes in weight and/or lipid profile and/or glucose metabolism in the intervention phase (Part 2). Note: Changes of the different components will be analyzed separately as secondary outcomes.
Time Frame
From baseline visit to close-out visit (Part 1: 4 weeks for adults, 2 weeks for teenagers; followed by Part 2: 6 months for adults, 6 weeks for teenagers)
Secondary Outcome Measure Information:
Title
Adherence to TRF intervention
Description
After allocation to the TRF arm, assessment of the adherence to the intervention, as measured by eating duration from the first to last caloric intake over 24-hour cycle.
Time Frame
From randomization visit to close-out visit (Part 2: 6 months for adults, 6 weeks for teenagers)
Title
Weight change
Description
Part of the composite primary outcome in the intervention phase (Part 2)
Time Frame
From baseline visit to close-out visit (Part 1: 4 weeks for adults, 2 weeks for teenagers; followed by Part 2: 6 months for adults, 6 weeks for teenagers)
Title
Change in lipid profile
Description
Part of the composite primary outcome in the intervention phase (Part 2)
Time Frame
From baseline visit to close-out visit (Part 1: 4 weeks for adults, 2 weeks for teenagers; followed by Part 2: 6 months for adults, 6 weeks for teenagers)
Title
Change in glucose metabolism
Description
Part of the composite primary outcome in the intervention phase (Part 2)
Time Frame
From baseline visit to close-out visit (Part 1: 4 weeks for adults, 2 weeks for teenagers; followed by Part 2: 6 months for adults, 6 weeks for teenagers)
Title
Change in blood pressure
Description
Systolic and diastolic blood pressure
Time Frame
From baseline visit to close-out visit (Part 1: 4 weeks for adults, 2 weeks for teenagers; followed by Part 2: 6 months for adults, 6 weeks for teenagers)
Title
Change in hepatic steatosis / fibrosis score
Description
As measured by the Fibroscan device
Time Frame
From randomization visit to close-out visit (Part 2: 6 months for adults, 6 weeks for teenagers)
Title
Change in number of meals per day
Description
Temporal analysis of caloric intake events collected by the smartphone app
Time Frame
From baseline visit to close-out visit (Part 1: 4 weeks for adults, 2 weeks for teenagers; followed by Part 2: 6 months for adults, 6 weeks for teenagers)
Title
Change in meal intervals
Description
Temporal analysis of caloric intake events collected by the smartphone app
Time Frame
From baseline visit to close-out visit (Part 1: 4 weeks for adults, 2 weeks for teenagers; followed by Part 2: 6 months for adults, 6 weeks for teenagers)
Title
Change in fraction of calories consumed after noon
Description
Estimation of caloric content from food pictures collected by the smartphone app
Time Frame
From baseline visit to close-out visit (Part 1: 4 weeks for adults, 2 weeks for teenagers; followed by Part 2: 6 months for adults, 6 weeks for teenagers)
Title
Change in fraction of calories consumed after 6pm
Description
Estimation of caloric content from food pictures collected by the smartphone app
Time Frame
From baseline visit to close-out visit (Part 1: 4 weeks for adults, 2 weeks for teenagers; followed by Part 2: 6 months for adults, 6 weeks for teenagers)
Title
Change in eating pattern difference between weekdays and weekends
Description
Indirect assessment of different lifestyle habits during weekdays and weekends
Time Frame
From baseline visit to close-out visit (Part 1: 4 weeks for adults, 2 weeks for teenagers; followed by Part 2: 6 months for adults, 6 weeks for teenagers)
Other Pre-specified Outcome Measures:
Title
Change in fat mass
Description
Body composition as measured by dual energy X-ray absorptiometry (DEXA)
Time Frame
From randomization visit to close-out visit (Part 3: 6 months, only adults)
Title
Change in fat free mass
Description
Body composition as measured by dual energy X-ray absorptiometry (DEXA)
Time Frame
From randomization visit to close-out visit (Part 3: 6 months, only adults)
Title
Change in diurnal rhythms of cortisol secretion
Description
Repeated measurements of cortisol over a 24-hour cycle
Time Frame
From randomization visit to close-out visit (Part 3: 6 months, only adults)
Title
Change in diurnal rhythms of melatonin secretion
Description
Repeated measurements of melatonin over a 24-hour cycle
Time Frame
From randomization visit to close-out visit (Part 3: 6 months, only adults)
Title
Change in physical activity
Description
As measured by actigraphy
Time Frame
From randomization visit to close-out visit (Part 3: 6 months, only adults)
Title
Change in sleep/wake cycles
Description
As measured by actigraphy
Time Frame
From randomization visit to close-out visit (Part 3: 6 months, only adults)
Title
Eating duration - alternative definition of the primary outcome
Description
Alternative definition of eating duration accounting for 2.5-97.5th percentiles of caloric intake over 24 hours, presumably less sensitive to the occasionally forgotten food picture event
Time Frame
From baseline visit to end of observation phase (Part 1: 4 weeks for adults, 2 weeks for teenagers)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Key inclusion criteria for both observation and intervention phases (Part 1+2): Age ≥ 12 years Body mass index ≥ 20 kg/m2 and stable weight (previous 3 months) in adults; BMI ≥ 25th percentile in teenagers Smartphone compatible with the app (iOS or Android systems) Additional inclusion criteria for the intervention phase (Part 2): Any component of the metabolic syndrome following the International Diabetes Federation consensus definition Eating duration >14h during the observation phase Additional inclusion criteria for the mechanistic study (Part 3): Age 18-40 years, men and pre-menopausal women BMI 30-40 kg/m2 In the fasting state (at least 8 hours) Key exclusion criteria for both observation and intervention phases (Part 1+2): Pregnant and breastfeeding women, plans for maternity during the study Major illness/fever over the previous month, active cancer Eating disorder, on a diet / weight management, prior bariatric surgery Major mental illness, unable to give informed consent Current shift work or travel abroad planned in the next month Additional exclusion criteria for the intervention phase (Part 2): Prior cardiovascular event Major liver, gastrointestinal, renal or endocrine disorder, diabetes mellitus with hypoglycemic drug(s) Major sleep disorder, centrally acting medication Lipid lowering drug, hypoglycemic drug, medication affecting the gut Additional exclusion criteria for the mechanistic study (Part 3): Impaired glucose tolerance (pre-diabetes) or diabetes mellitus Positive pregnancy test
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tinh-Hai Collet, MD
Organizational Affiliation
University of Lausanne Hospitals
Official's Role
Principal Investigator
Facility Information:
Facility Name
Inselspital, Klinik für Allgemeine Innere Medizin
City
Bern
State/Province
BE
ZIP/Postal Code
3010
Country
Switzerland
Facility Name
University Hospital of Lausanne (CHUV)
City
Lausanne
ZIP/Postal Code
1011
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Anonymized dataset of selected variables that underlie results in a publication. Some data may not be amenable to complete anonymization and will not be shared to ensure appropriate confidentiality of participant's data.
IPD Sharing Time Frame
Starting 6 months after publication
IPD Sharing Access Criteria
Upon appropriate data request by other scientists
Citations:
PubMed Identifier
33807102
Citation
Phillips NE, Mareschal J, Schwab N, Manoogian ENC, Borloz S, Ostinelli G, Gauthier-Jaques A, Umwali S, Gonzalez Rodriguez E, Aeberli D, Hans D, Panda S, Rodondi N, Naef F, Collet TH. The Effects of Time-Restricted Eating versus Standard Dietary Advice on Weight, Metabolic Health and the Consumption of Processed Food: A Pragmatic Randomised Controlled Trial in Community-Based Adults. Nutrients. 2021 Mar 23;13(3):1042. doi: 10.3390/nu13031042.
Results Reference
result
PubMed Identifier
34779776
Citation
Borloz S, Bucher Della Torre S, Collet TH, Jotterand Chaparro C. Consumption of Ultraprocessed Foods in a Sample of Adolescents With Obesity and Its Association With the Food Educational Style of Their Parent: Observational Study. JMIR Pediatr Parent. 2021 Nov 15;4(4):e28608. doi: 10.2196/28608.
Results Reference
result
PubMed Identifier
36239695
Citation
Papageorgiou M, Biver E, Mareschal J, Phillips NE, Hemmer A, Biolley E, Schwab N, Manoogian ENC, Gonzalez Rodriguez E, Aeberli D, Hans D, Pot C, Panda S, Rodondi N, Ferrari SL, Collet TH. The effects of time-restricted eating and weight loss on bone metabolism and health: a 6-month randomized controlled trial. Obesity (Silver Spring). 2023 Feb;31 Suppl 1(Suppl 1):85-95. doi: 10.1002/oby.23577. Epub 2022 Oct 14.
Results Reference
result
Links:
URL
http://www.swisschronofood.ch
Description
Study website

Learn more about this trial

Study of Eating Patterns With a Smartphone App and the Effects of Time Restricted Feeding in the Metabolic Syndrome

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