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Investigation of the Effects of Bariatric Surgery on Taste Reward in Humans

Investigation of the Effects of Bariatric Surgery on Taste Reward in Humans

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01531738
Enrollment
22
Registered
2012-02-13
Start date
2010-07-31
Completion date
2012-01-01
Last updated
2020-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Taste, bariatric surgery, food preferences, reward, progressive ratio task

Brief summary

The investigators hypothesize that some of these changes in the reduced appetite after surgery may be due to alterations in taste. The aim is to compare obese patients before and after bariatric surgery (gastric bypass and banding) to define the reward value of sweet, fatty and vegetable/fruit taste in obese individuals, and how this changes after surgery.

Detailed description

Severe obesity is associated with excessive food eating and appetite. Bariatric surgery (also known as 'obesity surgery' or 'weight loss surgery') is a well known treatment for severely obese individuals. The way in which these operations achieve weight loss is not fully understood. The investigators hypothesize that some of these changes in the reduced appetite after surgery may be due to alterations in taste. The aim is to compare obese patients before and after bariatric surgery (gastric bypass and banding) to define the reward value of sweet, fatty and vegetable/fruit taste in obese individuals, and how this changes after surgery.

Interventions

None listed

Sponsors

Medical Research Council
CollaboratorOTHER_GOV
Imperial College London
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* BMI of 18-25 for normal weight volunteers * BMI of \>30 for obese patients

Exclusion criteria

* Pregnancy * breast feeding * substance abuse * consumption of more than 3 alcoholic units per day * severe psychiatric illness * lack of understanding of test instructions * diabetes mellitus * chronic medical conditions making a general anaesthetic unsafe * allergy to stimulus ingredients * active smoking

Design outcomes

Primary

MeasureTime frameDescription
Breakpoints as Assessed by Change in the Number of Mouse Clicks in the Last Completed Ratio2 weeks pre and 8-12 weeks post operatively for surgical patients or on two occasions 10-14 weeks apart for normal weight control groupPatients were placed in front of a computer screen and a plate of 20 chocolate candies. The following prompt appeared on the screen: You can earn food by clicking on the mouse button. Click as much or as little as you like. When you no longer want to continue, press the spacebar to stop the session.Upon completion of each ratio a message box appeared on the screen: You have earned food. Enjoy your reward and after you have swallowed it completely you may click on OK to continue with the programme.After ingesting the reward, the patients pressed the OK button in the message box only if they wished to progress to the next ratio to obtain another chocolate candy. The starting ratio was 10 clicks with a geometric increment of 2 (i.e., 10, 20, 40, 80, and so on). When the effort of pressing the mouse button was greater than the rewarding value of the chocolate candy, patients pressed on the space bar to terminate the session. This indicated that the breakpoint was reached.

Secondary

MeasureTime frameDescription
Hunger2 weeks pre and 8-12 weeks post operatively for surgical patients or on two occasions 10-14 weeks apart for normal weight control groupVisual Analogue Scale ratings of hunger. The scale is 100mm line with two anchors at each end. Scores are recorded by making a handwritten mark that represents a continuum between not hungry at all and Extremely hungry. The score of 0 represents least hunger. The score of 100 represents extreme hunger. change in hunger levels quantified by a 100mm visual analogue scale
Body Mass Index2 weeks pre and 8-12 weeks post operatively for surgical patients or on two occasions 10-14 weeks apart for normal weight control groupchange in BMI will be quantified based on the participants weight in kilograms and height in meters

Countries

United Kingdom

Participant flow

Participants by arm

ArmCount
Control
Normal weight healthy volunteers
11
Bariatric Surgery
obese patients due to undergo gastric bypass or gastric banding
11
Total22

Baseline characteristics

CharacteristicControlBariatric SurgeryTotal
Age, Customized
Age
39 years
STANDARD_DEVIATION 5
49 years
STANDARD_DEVIATION 3
44 years
STANDARD_DEVIATION 4
BMI (kg/m^2)23 kg/m^2
STANDARD_DEVIATION 1
48 kg/m^2
STANDARD_DEVIATION 2
35.5 kg/m^2
STANDARD_DEVIATION 1.5
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
11 Participants11 Participants22 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Sex: Female, Male
Female
7 Participants7 Participants14 Participants
Sex: Female, Male
Male
4 Participants4 Participants8 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 110 / 11
other
Total, other adverse events
0 / 110 / 11
serious
Total, serious adverse events
0 / 110 / 11

Outcome results

Primary

Breakpoints as Assessed by Change in the Number of Mouse Clicks in the Last Completed Ratio

Patients were placed in front of a computer screen and a plate of 20 chocolate candies. The following prompt appeared on the screen: You can earn food by clicking on the mouse button. Click as much or as little as you like. When you no longer want to continue, press the spacebar to stop the session.Upon completion of each ratio a message box appeared on the screen: You have earned food. Enjoy your reward and after you have swallowed it completely you may click on OK to continue with the programme.After ingesting the reward, the patients pressed the OK button in the message box only if they wished to progress to the next ratio to obtain another chocolate candy. The starting ratio was 10 clicks with a geometric increment of 2 (i.e., 10, 20, 40, 80, and so on). When the effort of pressing the mouse button was greater than the rewarding value of the chocolate candy, patients pressed on the space bar to terminate the session. This indicated that the breakpoint was reached.

Time frame: 2 weeks pre and 8-12 weeks post operatively for surgical patients or on two occasions 10-14 weeks apart for normal weight control group

ArmMeasureValue (MEAN)Dispersion
ControlBreakpoints as Assessed by Change in the Number of Mouse Clicks in the Last Completed Ratio0 ClicksStandard Deviation 40
Bariatric SurgeryBreakpoints as Assessed by Change in the Number of Mouse Clicks in the Last Completed Ratio320 ClicksStandard Deviation 30
Secondary

Body Mass Index

change in BMI will be quantified based on the participants weight in kilograms and height in meters

Time frame: 2 weeks pre and 8-12 weeks post operatively for surgical patients or on two occasions 10-14 weeks apart for normal weight control group

ArmMeasureValue (MEAN)Dispersion
ControlBody Mass Index-0.2 kg/m^2Standard Deviation 1.2
Bariatric SurgeryBody Mass Index-6.2 kg/m^2Standard Deviation 1.6
Secondary

Hunger

Visual Analogue Scale ratings of hunger. The scale is 100mm line with two anchors at each end. Scores are recorded by making a handwritten mark that represents a continuum between not hungry at all and Extremely hungry. The score of 0 represents least hunger. The score of 100 represents extreme hunger. change in hunger levels quantified by a 100mm visual analogue scale

Time frame: 2 weeks pre and 8-12 weeks post operatively for surgical patients or on two occasions 10-14 weeks apart for normal weight control group

ArmMeasureValue (MEAN)Dispersion
ControlHunger20 mmStandard Deviation 30
Bariatric SurgeryHunger-60 mmStandard Deviation 30

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026