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THRIVE-Belize: A School-Based Life-Skills Program to Support Teen Health in Toledo District, Belize (Feasibility)

THRIVE-Belize: A Single-School Mixed-Methods Feasibility Trial of a Multi-Component Life-Skills Curriculum for Adolescent Health Promotion at Toledo Community College, Belize

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07687199
Acronym
THRIVE-Belize
Enrollment
280
Registered
2026-07-07
Start date
2026-07-01
Completion date
2026-09-01
Last updated
2026-07-07

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

Conditions

Adolescence, Feasibility Studies, Health Behavior

Keywords

feasibility study, school-based intervention, life skills, adolescents, Belize, implementation science, acceptability

Brief summary

THRIVE-Belize is a school-based program being developed to support the health and well-being of adolescents in the Toledo District of southern Belize. The program covers seven topics: communication and emotional regulation, healthy expressions of masculinity, sexual and reproductive health, healthy relationships, mental and physical health, substance use prevention, and environmental health. Before testing whether the program works, the research team needs to learn whether students, teachers, parents, school staff, and community members find it acceptable, appropriate, and practical to deliver at Toledo Community College. This study (Phase I) does not deliver the program to anyone. Instead, it gathers feedback through surveys, focus groups, and interviews with about 280 participants across these five groups. The information collected will be used to refine the program and decide whether to move forward to a future pilot study. No medical or educational intervention is given to participants in this phase.

Interventions

None listed

Sponsors

University of Arizona
Lead SponsorOTHER
Hillside Health Care
CollaboratorUNKNOWN
Toledo Community College
CollaboratorUNKNOWN

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* Students: enrolled at Toledo Community College in Forms 1-4; ages 12-18 years; able to read and comprehend English at grade level; provides written assent; has active written parental/guardian consent * Teachers: currently employed at TCC; teaches students in Forms 1-4; provides written informed consent * Parents/Guardians: parent or legal guardian of an eligible TCC student; age 18 years or older; able to communicate in English, Spanish, or Q'eqchi'-Mopan Maya; provides written informed consent * School Principal and Administrative Staff: currently serving as principal or administrative staff at TCC; provides written informed consent * Community Stakeholders: recognized expertise in adolescent health, education, or youth services (e.g., healthcare providers, religious leaders, village council members, youth organization leaders); resident of Toledo District, Belize; provides written informed consent

Exclusion criteria

* Cognitive or developmental limitations preventing informed assent or participation (students) * Declines to participate (students or parents/guardians)

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of the proposed intervention (AIM)Single timepoint at post-assessment data collection (study months 1-2)Mean score on the adapted 4-item Acceptability of Intervention Measure (AIM), 5-point Likert scale (1=Strongly Disagree to 5=Strongly Agree). A mean score of 4.0 or higher indicates acceptability.
Appropriateness of the proposed intervention (IAM)Single timepoint at post-assessment data collection (study months 1-2)Mean score on the adapted 4-item Intervention Appropriateness Measure (IAM), 5-point Likert scale. A mean score of 4.0 or higher indicates appropriateness.
Feasibility of the proposed intervention (FIM)Single timepoint at post-assessment data collection (study months 1-2)Mean score on the adapted 4-item Feasibility of Intervention Measure (FIM), 5-point Likert scale. A mean score of 4.0 or higher indicates feasibility.
Adoption and organizational readinessSingle timepoint at post-assessment data collection (study months 1-2)Proportion of stakeholders expressing intent to support or participate in the proposed intervention, supplemented by qualitative themes related to readiness and barriers from focus groups and interviews.

Secondary

MeasureTime frameDescription
Recruitment and consent feasibilityThroughout the recruitment period (study months 1-2)Consent/assent rates (target: at least 60%), retention rates, and reasons for non-participation.
Measurement feasibility and respondent burdenSingle timepoint at post-assessment data collection (study months 1-2)Survey completion rates (target: at least 90%), item-level missingness, and participant-reported comprehension of instruments.
Facilitator and delivery feasibilitySingle timepoint at post-assessment data collection (study months 1-2)Qualitative assessment of teacher capacity, willingness to deliver the curriculum (target: at least 60% willing), training needs, and scheduling constraints.

Countries

Belize

Contacts

CONTACTMario Morales, PhD
mariomorales@arizona.edu520-645-5878
CONTACTGabriela Valdez, PhD
gvaldez@arizona.edu520-626-6530

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 8, 2026