- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07239167
A Prospective Cohort Study on Patient With Obesity Undergoing Weight Change
This prospective cohort study collected baseline data and followed up obese patients at their first visit to a weight loss clinic. The study examined the impact of various predictors and biomarkers on weight loss outcomes, aiming to establish an evidence-based foundation for personalized weight loss treatment.
Participants underwent a battery of measurements and questionnaires, including height, weight, waist circumference, blood pressure, blood tests, and questionnaires addressing diet, exercise, stress, sleep, measure handgrip strength ,and psychological well-being.
Study Overview
Status
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Zhongzheng Dist
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Taipei, Zhongzheng Dist, Taiwan, 100
- No.7, Chung Shan S. Rd.(Zhongshan S. Rd.)
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults aged 18 years or older, regardless of gender.
- Body mass index (BMI) ≥ 27 kg/m², or ≥ 24 kg/m² with one or more obesity-related comorbidities.
- Willing to undergo any form of weight loss intervention.
- Able to read and understand Chinese, willing to complete questionnaires, blood tests, and follow-up follow-up.
- Voluntarily consent to participate and be willing to complete the subject consent form.
Exclusion Criteria:
- Pregnant or breastfeeding women.
- Individuals with significant mental illness (e.g., schizophrenia, severe depression) or cognitive impairment that may affect their ability to consent or cooperate with the study.
- Individuals with severe organ dysfunction (e.g., end-stage renal disease, cirrhosis, congestive heart failure, etc.).
- Individuals taking medications that significantly affect their weight (e.g., long-term steroids or antipsychotics) and cannot be discontinued.
- Individuals deemed unsuitable for participation in this study by the study leader (e.g., individuals who are expected to be unable to complete follow-up).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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A prospective cohort study on patients with obesity undergoing weight change
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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Baseline data were collected and followed up during the subjects' initial visit to the weight loss clinic to establish an evidence-based basis for personalized weight reduction treatment.
Time Frame: Weight changes of subjects after 24 weeks, 48 weeks, 72 weeks, and 96 weeks.
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Weight changes of subjects after 24 weeks, 48 weeks, 72 weeks, and 96 weeks.
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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 (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202504134RINA
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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