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Clinical Trials/NCT01531738
NCT01531738
Completed
Not Applicable

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

Imperial College London1 site in 1 country22 target enrollmentJuly 2010
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Imperial College London
Enrollment
22
Locations
1
Primary Endpoint
Breakpoints as Assessed by Change in the Number of Mouse Clicks in the Last Completed Ratio
Status
Completed
Last Updated
5 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
July 2010
End Date
January 1, 2012
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Carel Le Roux

Principal Investigator

Imperial College London

Eligibility Criteria

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

Outcomes

Primary Outcomes

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

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

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.

Secondary Outcomes

  • Hunger(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)
  • Body Mass Index(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)

Study Sites (1)

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