A Prospective Cohort Study on Patient With Obesity Undergoing Weight Change (NCT07239167) | Clinical Trial Compass
By InvitationNot Applicable
A Prospective Cohort Study on Patient With Obesity Undergoing Weight Change
Taiwan500 participantsStarted 2025-06-05
Plain-language summary
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.
Who can participate
Age range18 Years
SexALL
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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.
What they're measuring
1
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.
Timeframe: Weight changes of subjects after 24 weeks, 48 weeks, 72 weeks, and 96 weeks.
✕. 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).