Menu
Recruiting NCT05621278

Children to Adults Mental and Psychosomatic Health Study (CAMPS)

Observational Mental Health Wellness Cognitive Function Physical Symptoms

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Mental Health Wellness, Cognitive Function, Physical Symptoms. Basic parameters: 9 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Children to Adults Mental and Psychosomatic Health Study (CAMPS): A Longitudinal Cohort Study

Overview

This study titled the Children to Adults Mental and Psychosomatic Health Study (CAMPS), aims to explore the interplay between mental health, psychosomatic factors, and adverse childhood experiences (ACE) across a broad age range, from school-age children to adults in China. The study will involve participants from various educational settings, including teachers, students, and parents, who will be recruited through schools. The assessment methodology will combine validated psychometric scales and behavioral experiments to comprehensively evaluate mental and physical health aspects and the impact of ACEs. This integrative approach is designed to illuminate the complex relationships between psychological well-being, somatic symptoms, and early life stressors across different life stages.

Primary outcome measures

  • Irritability [Time frame: 1 month]
  • Alexithymia [Time frame: 1 month]
  • Depression for adults [Time frame: 2 weeks]
  • Depression [Time frame: 2 weeks]
  • Generalized anxiety disorder [Time frame: 2 weeks]
  • Anxiety and depression for adolescents and children [Time frame: 2 weeks]
  • PTSD for adults [Time frame: 1 month]
  • PTSD for adolescents and children [Time frame: 1 month]
  • NSSI [Time frame: 1 year]
  • Suicide [Time frame: 1 year]

Eligibility criteria

Inclusion criteria

  • Students from 5 grade to 12 grade, their parents and teachers
  • able to read, answer questionnaires and complete experiments.

Exclusion criteria

a. Students who suspend schooling.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Peking University — Beijing

Identifiers

NCT: NCT05621278 · CAMPS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗