- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03255304
Influence of Priming on Goal-directed and Cue-dependent Behavior
November 26, 2019 updated by: Sabine Frank, University Hospital Tuebingen
The current proposal aims to investigate implicit and explicit priming paradigms for changing cue-dependent and goal-directed nutritional behavior.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Food choice and intake is a daily and throughout normal subject.
However, for more and more people eating habits and the question of food choice are of increasing interest and in several cases even a problem.
The prevalence of obesity has tripled in the last decades and it is even spoken of an obesity epidemic.
Life style interventions to lose weight often fail on the long run, also because people fall back into former unhealthy eating habits.
Various factors influence our daily food choice, not all of which are apparent to ourselves.
Thus, food choice might be goal-directed and therefore conscious and reflective, yet in other circumstances the choice to eat something specific might be based on cue dependent processes which are automatic and thus difficult to control.
Since a change in eating-behavior and long-lasting weight loss is most problematic to achieve, the current proposal aims to investigate implicit and explicit priming paradigms for changing cue-dependent and goal-directed nutritional behavior.
Study Type
Interventional
Enrollment (Actual)
222
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Tübingen, Germany
- University of Tübingen
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 50 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- healthy volunteers
Exclusion Criteria:
- currently dieting
- intolerance to provided food
- cognitive impairment
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: health prime
|
groups be confronted with health aspects of food items
|
|
Experimental: palatability prime
|
groups be confronted with palatability aspects of food items
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
behavior
Time Frame: pre and post priming (directly before and directly after a 5 minutes priming paradigm)
|
change in food choice within a Pavlovian-to-instrumental transfer task (duration of complete protocol about 45 minutes, including priming (5 minutes) and pre and post measurements)
|
pre and post priming (directly before and directly after a 5 minutes priming paradigm)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2018
Primary Completion (Actual)
June 1, 2019
Study Completion (Actual)
June 1, 2019
Study Registration Dates
First Submitted
August 14, 2017
First Submitted That Met QC Criteria
August 18, 2017
First Posted (Actual)
August 21, 2017
Study Record Updates
Last Update Posted (Actual)
November 27, 2019
Last Update Submitted That Met QC Criteria
November 26, 2019
Last Verified
November 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- PIT_prime
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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