- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05553574
Inhibitory Capabilities Among Women With Eating Disorders
March 1, 2023 updated by: Shir Berebbi, Hebrew University of Jerusalem
The goal of the study is to increase the flexible behavior toward food via inhibition training among restrained eaters.
The expectation is that the train will increase food consumption, decrease food-related anxiety and affect implicit attitudes towards palatable foods
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
90
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
-
-
-
Jerusalem, Israel
- Hebrew University of Jerusalem
-
-
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 to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Diagnosis of restrained eaters
- Adults ages 18-40
Exclusion Criteria:
- Current history or diagnosis of the following according to the criteria of the DSM-5:
Schizophrenia, schizoaffective disorder, hallucinations, unspecified psychotic disorder (NOS), a mental disorder due to acquired head injury, bipolar disorder, mental disorder as a result of organic development.
- Abuse or addiction to drugs and alcohol.
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: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Food response
|
The participants need to classify pictures of food and not food.
They were asked to hold their response if they see a white frame around the picture.
|
Experimental: Food stop
|
The participants need to classify pictures of food and not food.
They were asked to hold their response if they see a white frame around the picture.
|
Experimental: Food response-inhibition
|
The participants need to classify pictures of food and not food.
They were asked to hold their response if they see a white frame around the picture.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Main outcome
Time Frame: one hour
|
The participants will increase food consumption,decrease food-related anxiety and affect implicit attitudes towards palatable foods
|
one hour
|
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)
March 8, 2021
Primary Completion (Anticipated)
December 30, 2023
Study Completion (Anticipated)
December 30, 2023
Study Registration Dates
First Submitted
May 26, 2021
First Submitted That Met QC Criteria
September 21, 2022
First Posted (Actual)
September 23, 2022
Study Record Updates
Last Update Posted (Actual)
March 2, 2023
Last Update Submitted That Met QC Criteria
March 1, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SB1
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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