- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04178486
Changing Eating Behaviors of Healthy Adults Through Hypnosis
November 25, 2019 updated by: Comsa Loana, Babes-Bolyai University
Eating Behavior - Choice or Reconstruction of Past Experience? Changing Eating Behaviors of Healthy Adults Through Hypnotic Suggestions
There is a lot of research on weight loss.
In spite of the research on the subject, obesity is a growing disease all through the world.
The results of recent reviews and meta-analyzes show that psychological interventions had small effect on weight loss.
The investigators propose a different approach to changing eating behaviors with relevance to weight management and hypothesize that participants in the active interventions will significantly improve their eating behaviors than the ones in the control group.
The results will improve the psychological interventions for weight loss.
Study Overview
Status
Completed
Conditions
Detailed Description
This is a randomized clinical trial consisting of four groups.
According to the concept of Free Will, the decision of action is taken before being acknowledged and is made following the reconstruction of previous experiences.
It can be inhibited immediately (max 100ms) after awareness.
The investigators want to intervene based on this model using hypnotic suggestions to change eating behaviors.
Participants were found through social media announcements.
Three groups receive one session of hypnosis with induction and different suggestions and the control group receives only induction.
The eating behavior is measured through computer tasks in which participants have the option to choose pictures of food.
The task is performed before, during and after hypnosis and the measurements of eating behavior are taken at all three times.
Study Type
Interventional
Enrollment (Actual)
89
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
-
-
Cluj
-
Cluj-Napoca, Cluj, Romania, 400015
- Department of Clinical Psychology and Psychotherapy
-
-
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
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
Both gender Healthy Adults who want to change their eating behavior
Exclusion Criteria:
Severe mental illness <18 years A diagnosed eating disorder
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: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Amnesia
Hypnosis formed from hypnotic induction (an adapted version from Barber Suggestibility Scale) together with hypnotic suggestions to experience amnesia for the food pictures they had just seen.
|
Participants received hypnotic induction with hypnotic suggestions for their eating behaviors.
|
|
EXPERIMENTAL: Cognitive Rehearsal
Hypnosis formed from hypnotic induction (an adapted version from Barber Suggestibility Scale) together with hypnotic suggestions about a future where they will control their eating behaviors.
|
Participants received hypnotic induction with hypnotic suggestions for their eating behaviors.
|
|
EXPERIMENTAL: Memory Substitution
Hypnosis formed from hypnotic induction (an adapted version from Barber Suggestibility Scale) together with hypnotic suggestions about a past where they have always controlled their eating behaviors.
|
Participants received hypnotic induction with hypnotic suggestions for their eating behaviors.
|
|
PLACEBO_COMPARATOR: Control
Hypnosis formed from only hypnotic induction (an adapted version from Barber Suggestibility Scale).
|
Participants received only hypnotic induction.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Eating Behavior
Time Frame: The intervention is delivered in one session. The outcome is measured: immediately pre intervention (0-2 min), during intervention and immediately post intervention (0-2 min).
|
The number of food pictures chosen by the participant in this single session intervention.
The outcome is a measure assessing a change between three time points.
|
The intervention is delivered in one session. The outcome is measured: immediately pre intervention (0-2 min), during intervention and immediately post intervention (0-2 min).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Loana T Comsa, Phd Student, Babes Bolyay University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Haggard P, Cartledge P, Dafydd M, Oakley DA. Anomalous control: when 'free-will' is not conscious. Conscious Cogn. 2004 Sep;13(3):646-54. doi: 10.1016/j.concog.2004.06.001.
- Jamieson GA, Kittenis MD, Tivadar RI, Evans ID. Inhibition of retrieval in hypnotic amnesia: dissociation by upper-alpha gating. Neurosci Conscious. 2017 Apr 19;2017(1):nix005. doi: 10.1093/nc/nix005. eCollection 2017.
- Gravitz, Melvin A.
- Oakley DA, Halligan PW. Hypnotic suggestion and cognitive neuroscience. Trends Cogn Sci. 2009 Jun;13(6):264-70. doi: 10.1016/j.tics.2009.03.004. Epub 2009 May 8.
- Obhi, Sukhvinder S., and Patrick Haggard.
- Kuhn S, Haggard P, Brass M. Intentional inhibition: how the "veto-area" exerts control. Hum Brain Mapp. 2009 Sep;30(9):2834-43. doi: 10.1002/hbm.20711.
- Wolpert DM, Ghahramani Z, Jordan MI. An internal model for sensorimotor integration. Science. 1995 Sep 29;269(5232):1880-2. doi: 10.1126/science.7569931.
- Haggard P. Human volition: towards a neuroscience of will. Nat Rev Neurosci. 2008 Dec;9(12):934-46. doi: 10.1038/nrn2497.
- Libet, Benjamin.
- Terhune DB, Brugger P. Doing better by getting worse: posthypnotic amnesia improves random number generation. PLoS One. 2011;6(12):e29206. doi: 10.1371/journal.pone.0029206. Epub 2011 Dec 15.
- Mendelsohn A, Chalamish Y, Solomonovich A, Dudai Y. Mesmerizing memories: brain substrates of episodic memory suppression in posthypnotic amnesia. Neuron. 2008 Jan 10;57(1):159-70. doi: 10.1016/j.neuron.2007.11.022.
- Oakley DA, Halligan PW. Hypnotic suggestion: opportunities for cognitive neuroscience. Nat Rev Neurosci. 2013 Aug;14(8):565-76. doi: 10.1038/nrn3538. Epub 2013 Jul 17.
- Stoeckel LE, Weller RE, Cook EW 3rd, Twieg DB, Knowlton RC, Cox JE. Widespread reward-system activation in obese women in response to pictures of high-calorie foods. Neuroimage. 2008 Jun;41(2):636-47. doi: 10.1016/j.neuroimage.2008.02.031. Epub 2008 Mar 4.
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 20, 2019
Primary Completion (ACTUAL)
September 17, 2019
Study Completion (ACTUAL)
September 17, 2019
Study Registration Dates
First Submitted
October 27, 2019
First Submitted That Met QC Criteria
November 25, 2019
First Posted (ACTUAL)
November 26, 2019
Study Record Updates
Last Update Posted (ACTUAL)
November 26, 2019
Last Update Submitted That Met QC Criteria
November 25, 2019
Last Verified
November 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Phd Study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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