CClinicalTrials.gg
CompletedNCT03894670PRESETUpdated Jun 18, 2019

Evaluation of Methods for Measuring Gastrointestinal Transit and Food Reward in Healthy Individuals - The PRESET Study

An interventional study of Standard mixed breakfast meal and SmartBar™ in Healthy Participants, sponsored by Kristine Færch. Completed at 1 site in Denmark. Open to participants aged 30 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-06-18.

Sponsored by Kristine Færch · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Oct 2018, registered Mar 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Randomized
Ages
30 Years to 70 Years
Sex
All
01

Study summary

The wireless motility capsule technology, SmartPill™, can be used to assess gastric emptying and gastrointestinal (GI) transit time. The SmartPill is usually ingested together with a SmartBar™ which is a snack bar with a nutrient composition that differs substantially from a normal western diet. The primary aim of the present study is to compare effects of a SmartBar™ and a standard mixed meal on gastric emptying and GI motility.

Read the detailed description

Background: The wireless motility capsule technology, SmartPill™, can be used to assess GI transit time including gastric emptying and small and large bowel transit time based on measurements of pH, pressure and temperature. The SmartPill™ allows for GI motility measurements under free-living conditions without radiation. The SmartPill is usually ingested together with a SmartBar™ which is a snack bar with a nutrient composition that differs substantially from a normal western diet. GI motility in response to meals plays an important role in regulation of e.g. appetite and glucose metabolism. Changes in appetite and metabolism in response to interventions are often assessed using a meal test and GI motility is assessed at the research facilities. The use of SmartPill™ in combination with a meal test would allow for assessment of GI motility under subsequent free-living conditions and improve our understanding of the effects of interventions on the integrative relationship between food intake, GI motility and metabolism. Most of our daily decisions and actions affecting energy intake are driven by the non-conscious processes; however, appetite is often assessed from participants' self-report which is associated with limitations such as desire to report socially desirable answers. Little is known about the complex interrelationship between biological markers of appetite e.g. GI hormones and subjective and objective measures of food related behavior under fasting and fed conditions.

The PRESET study has the following objectives:

  1. To compare effects of a SmartBar™ and a standard mixed breakfast meal on gastric emptying and GI transit time measured using the SmartPill™ in normal-weight individuals.
  2. To compare effects of a SmartBar™ and a standard mixed breakfast meal on concentrations of metabolites and pancreatic and GI hormones, and subjective and objective measures of appetite, food reward and food related behavior assessed from biometric responses (facial expression, galvanic skin response and eye tracking) to visual food stimuli varying in fat content and taste during the computerized Leeds Food Preference Questionnaire (LFPQ) in normal-weight individuals.
  3. To assess potential associations between gastric emptying and GI motility, biological markers of appetite and subjective appetite and objective measures of food related behavior from biometric responses to visual food stimuli during the LFPQ in the fasting state and in response to meals in normal-weight individuals.

Testing includes assessments in the fasting state and in response to consumption of the SmartBar™ and a standard mixed meal (4-hour meal tests and subsequent 6-days free-living assessment period) on two separate test days.

02

Conditions studied

  • Healthy Participants

Keywords

  • Gastric emptying
  • Gastrointestinal transit
  • Food reward
  • Food preferences
03

In context

Lead sponsor

Kristine Færch is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Body mass index: 18.5 to 24.9 kg/m2

Exclusion criteria

Exclusion Criteria:

  • Unable to understand the informed consent and the study procedures;
  • Self-reported history of an eating disorder in the past three years
  • Self-reported weight change (>5 kg) within three months prior to inclusion
  • HbA1c: ≥5.7 % (≥39 mmol/mol)
  • Uncontrolled medical issues including but not limited to cardiovascular pulmonary, rheumatologic, hematologic, oncologic, infectious, GI or psychiatric disease; diabetes or other endocrine disease; immunosuppression
  • Current treatment with medication or medical devices which affect GI motility and transit time (prokinetics, antidiarrheals, laxatives)
  • Current treatment with medication which affect glucose metabolism or appetite
  • Current treatment with beta blockers or peroral steroids
  • Current treatment with non-steroidal anti-inflammatory drugs, tricyclic antidepressants, selective serotonin re-uptake inhibitors or opioids
  • Bariatric surgery
  • GI symptoms or diseases such as regular (weekly) abdominal pain, dysphagia, gastric bezoars, strictures, fistulas, bowel obstructions, diverticulitis, celiac disease, Crohn's disease, ulcerative colitis or proctitis
  • Alcohol/drug abuse or in treatment with disulfiram (Antabus) at time of inclusion
  • Pregnant or lactating women
  • Fertile women not using birth control agents including oral contraceptives, gestagen injection, subdermal implants, hormonal vaginal ring, transdermal application, or intra-uterine devices
  • Concomitant participation in other research studies
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
15 participants (actual)

Study arms

  • Active comparator
    SmartBar™

    The wireless capsule technology, SmartPill™, is usually ingested together with a SmartBar™ which is a snack bar with a nutrient composition that differs substantially from a normal western diet.

    Other: SmartBar™

  • Experimental
    Standard mixed breakfast meal

    The SmartPill™ is ingested together with a standard mixed breakfast meal and the outcomes of interest will be compared with the SmartBar™ condition (reference).

    Other: Standard mixed breakfast meal

Interventions

  • OtherStandard mixed breakfast meal

    The standard mixed breakfast meal consists of: 150 g yoghurt, 20 g muesli; 50 g wheat bun; 22 g rye bread; 25 g cheese; 25 g marmalade; 8 g butter; Total energy content: 500 kcal Macronutrient composition: 34 E% fat, 17 E% protein, 49 E% carbohydrate

  • OtherSmartBar™

    SmarBar™ (Medtronic, North Haven, MA, USA). Weight: 72 g; Total energy content: 260 kcal Macronutrient composition: 7 E% fat, 19 E% protein, 74 E% carbohydrate.

06

What researchers measure

Primary outcomes

  1. Gastric emptying time (minutes)

    Measured by the SmartPill™ technique. The SmartPill™ is ingested at both visits in combination with the standard breakfast meal and SmartBar™, respectively. The time frame depends on the individual gastric emptying time.

    Time frame: Within 24 hours from ingestion of the SmartPill™ at both visits (standard breakfast meal and SmartBar™, respectively)

Secondary outcomes

  1. Small bowel transit time (minutes)

    Measured by the SmartPill™ technique. The SmartPill™ is ingested at both visits in combination with the standard breakfast meal and SmartBar™, respectively. The time frame depends on the individual transit time.

    Time frame: Within 5 days after both visits (standard breakfast meal and SmartBar™, respectively)

  2. Large bowel transit time (minutes)

    Measured by the SmartPill™ technique. The SmartPill™ is ingested at both visits in combination with the standard breakfast meal and SmartBar™, respectively. The time frame depends on the individual transit time.

    Time frame: Within 5 days after both visits (standard breakfast meal and SmartBar™, respectively)

  3. Total gastrointestinal transit time (minutes)

    Measured by the SmartPill™ technique. The SmartPill™ is ingested at both visits in combination with the standard breakfast meal and SmartBar™, respectively. The time frame depends on the individual transit time.

    Time frame: Within 5 days after both visits (standard breakfast meal and SmartBar™, respectively)

  4. Motility index (arbitrary unit)

    Calculated based on amplitudes and number of contractions measured using the SmartPill™ technique. The greater the motility index the greater the gastrointestinal motility (i.e. more frequent and stronger contractions). A higher motility index has been observed among healthy participants compared to patients with diabetic gastroparesis indicating that a higher index is favorable.

    Time frame: Within 5 days after both visits (standard breakfast meal and SmartBar™, respectively)

  5. Metabolites

    Concentrations of metabolites (including but not limited to: glucose, lipids, cholesterol, free-fatty acids, and amino acids. Measured at both visits in the fasting state and for 4 hours after consumption of the standard breakfast meal and the SmartBar™, respectively.

    Time frame: 0 minutes (fasting) and 15, 30, 45, 60, 90, 120, 180, 240 minutes (after consumption of the standard breakfast meal and SmartBar™, respectively)

  6. Hormones

    Concentrations of hormones related to regulation of appetite, glucose and lipid metabolism (including but not limited to: insulin, glucagon, ghrelin, glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP) and peptide YY (PYY), leptin, fibroblast growth factor 19 (FGF-19), fibroblast growth factor 21 (FGF-21), growth differentiation factor 15 (GDF-15)).

    Time frame: 0 minutes (fasting) and 15, 30, 45, 60, 90, 120, 180, 240 minutes (after consumption of the standard breakfast meal and SmartBar™, respectively)

  7. Attention measured using eye tracking

    Eye tracking metrics including gaze duration bias, gaze direction bias, fixations, saccades, pupil size/dilation, distance to screen, ocular vergence and blinks to measure attention in response to looking at food pictures during the computerized Leeds Food Preference Questionnaire

    Time frame: 0 minutes (fasting) at 60 minutes (after consumption of the standard breakfast meal and SmartBar™, respectively)

  8. Arousal measured using galvanic skin response

    Changes in conductivity of skin (galvanic skin response) in response to looking at food pictures during the computerized Leeds Food Preference Questionnaire

    Time frame: 0 minutes (fasting) and after 60 minutes (after consumption of the standard breakfast meal and SmartBar™, respectively)

  9. Emotions measured using facial expression analysis

    Facial expression analyses using computer-vision algorithms (AFFDEX) to measure emotions in response to looking at food pictures during the computerized Leeds Food Preference Questionnaire

    Time frame: 0 minutes (fasting) and after 60 minutes (after consumption of the standard breakfast meal and SmartBar™, respectively)

  10. Food choice

    Food choice of food items from four combined food categories (high-fat savoury, high-fat sweet, low-fat savoury and low-fat sweet foods) examined from the computerized Leeds Food Preference Questionnaire. Food choice is determined based on frequency of selection made within each food category. The scores range from 0-48 i.e. 0 = foods within a specific food category have not been selected at all to 48 = foods within a specific food category have been selected 48 times.

    Time frame: 0 minutes (fasting) and after 60 minutes (after consumption of the standard breakfast meal and SmartBar™, respectively)

  11. Implicit wanting

    Implicit wanting of food items from four combined food categories (high-fat savoury, high-fat sweet, low-fat savoury and low-fat sweet foods) examined from the computerized Leeds Food Preference Questionnaire. Implicit wanting is assessed based on food choice and response time for selected and non-selected food items as well as mean response time.

    Time frame: 0 minutes (fasting) and after 60 minutes (after consumption of the standard breakfast meal and SmartBar™, respectively)

  12. Explicit liking

    Explicit liking of 16 food items from four combined food categories (high-fat savoury, high-fat sweet, low-fat savoury and low-fat sweet foods) examined from the computerized Leeds Food Preference Questionnaire. Explicit liking is rated using visual analogue scales and the range is 0-100. Each end represents the extremes e.g. Question: "how pleasant would it be to taste this food right now?" Answer: "not at all" (rated 0 on the 0-100 scale) to "extremely" (rated 100 on the 0-100 scale).

    Time frame: 0 minutes (fasting) and after 60 minutes (after consumption of the standard breakfast meal and SmartBar™, respectively)

  13. Explicit wanting

    Explicit wanting of 16 food items from four combined food categories (high-fat savoury, high-fat sweet, low-fat savoury and low-fat sweet foods) examined from the computerized Leeds Food Preference Questionnaire. Explicit wanting is rated using visual analogue scales and the range is 0-100. Each end represents the extremes e.g. Question: "how much do you want some of this food now?" Answer: "not at all" (rated 0 on the 0-100 scale) to "extremely" (rated 100 on the 0-100 scale).

    Time frame: 0 minutes (fasting) and after 60 minutes (after consumption of the standard breakfast meal and SmartBar™, respectively)

  14. Subjective appetite

    Rated using visual analogue scales and includes sensations of: Hunger, fullness, satiety, prospective food consumption, wellbeing, nausea, thirst, desire to eat meat, salty, and sweet. The scale range is 0-100 and each end represent the extremes e.g. hunger rating: "I am not hungry at all" to "I have never been this hungry before".

    Time frame: 0 minutes (fasting) and 15, 30, 45, 60, 90, 120, 180, 240 minutes (after consumption of the standard breakfast meal and SmartBar™, respectively)

  15. Self-reported gastrointestinal symptoms (part 1)

    Assessed from the questionnaire the Gastrointestinal Symptom Rating Scale (GSRS). Rated on 7-point likert scales. Range: 1 = absence of symptoms to 7 = very severe symptoms.

    Time frame: Answered during test days (0-240 minutes)

  16. Self-reported gastrointestinal symptoms (part 2)

    Assessed from the Gastrointestinal Symptom Score (PAGI-SYM). Rated on 6-point likert scales. Range: 1 = absence of symptoms to 6 = very severe symptoms.

    Time frame: Answered during test days (0-240 minutes)

  17. Self-reported gastrointestinal symptoms (part 3)

    Number of symptoms. Assessed from logs.

    Time frame: Registered 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  18. Self-reported autonomic symptoms

    Assessed from the questionnaire COMPASS31

    Time frame: Answered during test days (0-240 minutes)

  19. Body weight (kg)

    Body weight is measured on a digital scale

    Time frame: At 0 minutes (fasting) at both visits

  20. Body mass index (kg/m^2)

    Calculated from body weight (kg) and height (m)

    Time frame: At 0 minutes (fasting) at both visits

  21. Fat mass (kg)

    Measured by Dual-energy X-ray Absorptiometry

    Time frame: At 0 minutes (fasting) at both visits

  22. Fat percentage (%)

    Measured by Dual-energy X-ray Absorptiometry

    Time frame: At 0 minutes (fasting) at both visits

  23. Fat free mass (kg)

    Measured by Dual-energy X-ray Absorptiometry

    Time frame: At 0 minutes (fasting) at both visits

  24. Waist circumference (cm)

    Measured using tape measure

    Time frame: At 0 minutes (fasting) at both visits

  25. Hip circumference (cm)

    Measured using tape measure

    Time frame: At 0 minutes (fasting) at both visits

  26. Mean amplitude of glycaemic excursions (MAGE)

    Measured using continous glucose monitoring

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  27. Continuous overall net glycaemic action (CONGA)

    Measured using continous glucose monitoring

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  28. Daily time spent above different glucose concentrations (e.g. >6.1 mmol/L, >7.0 mmol/L, >7.8 mmol/L, and >11.1 mmol/L)

    Measured using continous glucose monitoring

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  29. Mean glucose concentrations

    Measured using continous glucose monitoring

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  30. Standard deviation of glucose concentrations

    Measured using continous glucose monitoring

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  31. Variation coefficients of glucose concentrations

    Measured using continous glucose monitoring

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  32. Resting energy expenditure (kcal/day)

    Measured by indirect calorimetry under resting and fasting conditions

    Time frame: At 0 minutes (fasting) at both visits

  33. Substrate oxidation (respiratory exchange ratio)

    Measured by indirect calorimetry under resting and fasting conditions

    Time frame: At 0 minutes (fasting) at both visits

  34. Systolic blood pressure (mmHg)

    Measured under resting and fasting conditions

    Time frame: At 0 minutes (fasting) at both visits

  35. Diastolic blood pressure (mmHg)

    Measured under resting and fasting conditions

    Time frame: At 0 minutes (fasting) at both visits

  36. Heart rate (bpm)

    Measured under resting and fasting conditions during measurements of blood pressure and in the supine position by a handheld ECG measuring device (Vagus™).

    Time frame: At 0 minutes (fasting) at both visits

  37. Heart rate response to standing up from the supine position

    Measured by a handheld ECG measuring device (Vagus™).

    Time frame: At 0 minutes (fasting) at both visits

  38. Heart rate response to inhalation and exhalation

    Measured by a handheld ECG measuring device (Vagus™).

    Time frame: At 0 minutes (fasting) at both visits

  39. Heart rate response to forced exhalation during rest (valsalva maneuver)

    Measured by a handheld ECG measuring device (Vagus™).

    Time frame: At 0 minutes (fasting) at both visits

  40. Microbiome content and diversity

    Determined from stool samples. Bacterial DNA and RNA will be purified from the stool samples and changes in the microbiome composition and function will be estimated based on sequencing of the microbiomes' DNA and RNA. Includes but is not limited to the Firmicutes/Bacteroidetes ratio.

    Time frame: One sample during 6 days after both visits

  41. Physical activity (time spent at different intensities)

    Sedentary time, light, moderate and vigorous intensity physical activity. Assessed from 24 h/day accelerometry

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  42. Physical activity (counts/min)

    Assessed from 24 h/day accelerometry

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  43. Physical activity energy expenditure (kcal/day)

    Assessed from 24 h/day accelerometry

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  44. Physical activity (MET hours)

    Assessed from 24 h/day accelerometry

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  45. Timing of physical activity (hh:mm)

    Assessed from activity logs and 24 h/day accelerometry

    Time frame: Measured for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  46. Energy intake (kcal/day)

    Assessed from diet records

    Time frame: Assessed for 3 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  47. Macronutrient intake (energy percentage)

    Assessed from diet records

    Time frame: Assessed for 3 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  48. Timing of dietary intake (hh:mm)

    Assessed from diet records

    Time frame: Assessed for 3 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  49. Sleep timing (hh:mm)

    Including bedtime, sleep onset, wake-up, time out of bed, sleep midpoint. Assessed from sleep logs and 24 h/day accelerometry

    Time frame: Assessed for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  50. Sleep duration (minutes)

    Assessed from sleep logs and 24 h/day accelerometry

    Time frame: Assessed for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  51. Sleep variability (minutes)

    Variability in bedtime, wake-up, sleep duration and sleep midpoint. Assessed from sleep logs and 24 h/day accelerometry

    Time frame: Assessed for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  52. Sleep onset latency (minutes)

    Assessed from sleep logs and 24 h/day accelerometry

    Time frame: Assessed for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  53. Sleep efficiency (%)

    Assessed from 24 h/day accelerometry

    Time frame: Assessed for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  54. Wakefulness (minutes)

    Assessed from 24 h/day accelerometry

    Time frame: Assessed for 6 days after both visits (standard breakfast meal and the SmartBar™ conditions)

  55. HbA1c (mmol/mol and %)

    Hemoglobin A1c

    Time frame: At 0 minutes at both visits

  56. Insulin sensitivity (indices)

    Including but not limited to the Matsuda index

    Time frame: At 0 minutes (fasting) and 4 hours after consumption of the standard breakfast meal and the SmartBar™, respectively

  57. Insulin resistance (indices)

    Including but not limited to Homeostatic Model Assessment for Insulin Resistance (HOMA-IR)

    Time frame: At 0 minutes (fasting) and 4 hours after consumption of the standard breakfast meal and the SmartBar™, respectively

07

Study locations

1 site
  • Steno Diabetes Center Copenhagen
    Gentofte, DK-2810, Denmark
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03894670
Lead sponsor
Kristine Færch
Collaborators
University of Copenhagen, IMotions A/S, University of Leeds, Aalborg University Hospital
Responsible party
Kristine Færch (Senior Researcher and Team Leader, PhD, Steno Diabetes Center Copenhagen) — Sponsor-investigator
First posted
Mar 28, 2019
Start date
Oct 16, 2018
Primary completion
May 24, 2019
Completion
May 24, 2019
Last update
Jun 18, 2019

Study contacts

Kristine Færch, PhD
principal investigator · Steno Diabetes Center Copenhagen

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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