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Peer-Supported E-Health Intervention for College Student Weight Management and Mental Health

J

Jinan University Guangzhou

Status

Completed

Conditions

Obesity Prevention
Psychological Well Being
Depression - Major Depressive Disorder

Treatments

Behavioral: Peer Support Intervention
Behavioral: Peer Support and eHealth Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06966661
2025LCLL-057

Details and patient eligibility

About

This study will test whether adding peer support and online education can help college students manage their weight and improve their mood: we plan to enroll 300 full-time university students and randomly assign them to one of three six-month groups (monthly in-person health talks and weekly emailed tips alone; those activities plus biweekly peer-mentor meetings and an online chat group; or those activities plus a custom app delivering weekly lessons, monthly expert live Q&A, and self-tracking tools). We will measure weight, body mass index (BMI), and scores on standard questionnaires for depression (PHQ-9), anxiety (GAD-7) and life satisfaction (SWLS) at baseline, three months and six months to compare the effectiveness of each approach. By identifying which combination of face-to-face support and digital tools produces the greatest improvements, we aim to inform low-cost, scalable programs to help students maintain a healthy weight and emotional well-being.

Enrollment

216 patients

Sex

All

Ages

18 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Full-time undergraduate students aged 18-25 years
  • Baseline BMI ≥ 24.0 kg/m²
  • Able to provide informed consent
  • Owns a smartphone or computer with internet access
  • Willing to attend monthly lectures and complete online modules

Exclusion criteria

  • Current participation in another weight-management or psychological intervention program
  • Diagnosis of an eating disorder, severe psychiatric illness, or medical condition affecting weight (e.g., hyperthyroidism)
  • Pregnant or planning pregnancy during the study period
  • Any physical limitation precluding participation in light-to-moderate physical activity
  • Inability to communicate in the language of intervention materials

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

216 participants in 3 patient groups

Control Arm
No Intervention group
Peer Support Arm
Experimental group
Treatment:
Behavioral: Peer Support Intervention
Peer Support eHealth Arm
Experimental group
Treatment:
Behavioral: Peer Support and eHealth Intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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