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Integrated Weight Loss Program in Community-Dwelling Adults

Integrated Weight Loss Program in Community-Dwelling Adults: A Dual Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104420
Enrollment
Unknown
Registered
2025-06-17
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

overweight or obesity

Interventions

Routine Group:For family physicians (FPs): Standardized training in essential weight management competencies. For Participants: Provision of core health education covering obesity-related risks, healt
individualized lifestyle recommendations delivered by FPs
and three standardized biometric assessments.
Standard Group:For FPs (building upon Routine Group): Supplemental advanced training in weight management strategy formulation and personalized coaching. For Participants (building upon Routine Group)
digital self-monitoring of weight/diet/activity/sleep via study-provided platform with adherence-based incentive points
access to obesity risk/healthy behavior digital knowledge modules
and adaptive goal adjustment guided by regular biometric/lifestyle analytics reports.
Intensive Group:For FPs (building upon Standard Group): Digital upskilling through the study platform and remote collaborative management including data review with virtual feedback provision. For Par

Sponsors

School of Population Medicine and Public Health, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: (1) Aged >=18 years and =1 year with no plans for extended absence (>4 weeks) during the study period (4) Neither pregnant nor lactating (5) No plans for anti-obesity medication or bariatric surgery within 2 years (6) Willing to provide written informed consent

Exclusion criteria

Exclusion criteria: (1) History of malignancy (except locally cured basal cell carcinoma) (2) Clinically diagnosed psychiatric disorders (e.g., major depressive disorder requiring pharmacotherapy) (3) Severe comorbidities or functional impairments preventing completion of study procedures (4) Current participation in weight management clinical trials

Design outcomes

Primary

MeasureTime frame
Body Weight;

Secondary

MeasureTime frame
Body mass index;Obesity rate;Body fat percentage;Body composition;Blood pressure;Blood routine;liver function;Renal function;Inflammatory factor;Blood glucose (fasting blood glucose, glycated hemoglobin);Pancreas islet function;Hormone;Metabolome;Intestinal flora;Urine routine;Urinary chemistry (urinary creatinine, urinary microalbumin);Lifestyle (diet, physical activity, smoking, alcohol, sleep);Mental and psychological states (depression, anxiety, stress);Appetite;Self-efficacy;Health economics indicators;Implemental indicators (fidelity, adoption, other implemental indicators);blood lipid;

Countries

China

Contacts

Public ContactRuitai Shao

School of Population Medicine and Public Health, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

shaoruitai@cams.cn+86 139 1164 4595

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026