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Effect of the 3C Model in Students and Teachers From Vaupés, Boyacá and Amazonas

Efecto Del Modelo Conmigo, Contigo y Con Todos (3Cs) en Niños, Niñas y Adolescentes y Sus Profesores en Vaupés, Boyacá y Amazonas

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05378412
Enrollment
6000
Registered
2022-05-18
Start date
2023-01-31
Completion date
2025-12-31
Last updated
2022-05-18

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

Conditions

Resilience, Compassion

Brief summary

This study will evaluate the effectiveness of the 3Cs - Conmigo, Contigo y Con todo strategy in strengthening resilience and compassion in students and teachers from three regions from Colombia: Vaupés, Amazonas and Boyacá. It will also evaluate its relevance in the design of programs aimed at mental health in educational settings.

Detailed description

Colombia has experienced a long-lasting internal armed conflict that has impacted society at all levels and on people of all ages. This has led to changes in behavior and the way people cope with psychosocial distress. Focusing on children and adolescents, this study aims to assess the effectiveness of the 3Cs - Conmigo, Contigo y Con todo strategy in strengthening resilience and compassion. The changes in the scores of the CD-RISC and ECOM instruments will be evaluated through a mixed methods analysis that will evaluate the pre and post intervention results and the perception of all the actors involved in the development and implementation of the 3Cs program.

Interventions

BEHAVIORAL3Cs

The 3Cs program is an educational strategy aimed at fostering resilience and compassion in people. It is based on improving the mental well-being of the participants by transforming their attitudes and behaviors through increased consciousness.

Sponsors

Pontificia Universidad Javeriana
CollaboratorOTHER
Ministerio de Ciencia, Tecnología e Innovación
CollaboratorUNKNOWN
Fundación Saldarriaga Concha
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

This study is based on a mixed-methods experimental design and concurrent triangulation

Eligibility

Sex/Gender
ALL
Age
5 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Students and teachers from public institutions

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
CD-RISC36 monthsCD-RISC score
ECOM36 monthsECOM score

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026