- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04833803
Development of the Eating Behaviour Lapse Inventory Survey Singapore (eBLISS):An Exploratory Mixed-method Study
April 5, 2021 updated by: Jocelyn Chew, National University Health System, Singapore
An exploratory mixed-method study will be conducted to develop an instrument for early detection and prevention of overconsumption.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
530
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jocelyn Chew, PhD
- Phone Number: +6565168687
- Email: jocelyn.chew.hs@nus.edu.sg
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
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients who are overweight or obese and are following up at the Centre for Obesity Management and Surgery (COMS) at the National University Hospital (NUH).
Description
Inclusion Criteria:
- Above the legal age of 21 years old
- Have a BMI ≥ 23kg/m2
- Able to understand and read English language
- Uses a smart phone that can download apps
- Able to provide informed consent
Exclusion Criteria:
- Diagnosed with a pre-existing psychological disorder such as anxiety and depression except binge eating disorder
- Participating in a concurrent weight management intervention that is beside the usual care
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Self-regulation of Eating Behaviour Questionnaire (SREBQ)
Time Frame: 2021-2023
|
2021-2023
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
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 (Anticipated)
April 12, 2021
Primary Completion (Anticipated)
March 22, 2023
Study Completion (Anticipated)
March 22, 2023
Study Registration Dates
First Submitted
April 5, 2021
First Submitted That Met QC Criteria
April 5, 2021
First Posted (Actual)
April 6, 2021
Study Record Updates
Last Update Posted (Actual)
April 6, 2021
Last Update Submitted That Met QC Criteria
April 5, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 2020/01439
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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