In-depth Survey for the Reasons of Weight Control Difficulties (Weight Control)
Study Overview
Detailed Description
The aim of this study was to investigate the causes of weight control difficulties in overweight or obese patients of all ages by in-depth interview, in order to explore more causes of weight control difficulties, to make early exploration for targeted large-scale cross-sectional survey studies on the causes of weight control difficulties in the future, and to find the causes of weight control difficulties, which will help to study measures to solve weight control difficulties.
Study design: Overweight or obese Chinese patients were enrolled. According to their age, 3 males and 3 females (24 in total) aged 14-20 years, 21-40 years, 41-60 years and 61-80 years were included for interview for about 1 hour. The interview included demographic basic information and other characteristics, time and results of weight control, and causes of weight control difficulties. After collecting the information, classification and summary analysis were performed.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Beijing, China
- Peking Union Medical College Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Fully understand the purpose, nature and method of the study, voluntarily participate in the study, agree to record the interview content through a tape recorder during the interview, and sign the informed consent form (ICF) before the interview;
- Chinese aged 14-80 years (including boundary value, subject to the time of signing the informed consent form), male or female;
- Patients with body mass index (BMI) greater than 24 kg/m 2 , who have taken any weight control measures;
- Willing and able to comply with study requirements. -
Exclusion Criteria:
1. Inability to communicate in speech; 2. Known mental or psychological disorder of any kind; 3. Other conditions that, in the opinion of the investigator, would make participation in this study inappropriate.
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Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Obesity
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It is a qualitatative research.
Only a survey.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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Reasons of weight control difficulty
Time Frame: Before the time of interview
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Before the time of interview
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- O-BW-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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