Latino Teen Pregnancy Prevention K23

Part of paid clinical trials in Kansas City, Missouri.

Sponsor
Children's Mercy Hospital Kansas City
Study ID
NCT06105905
Status
Enrolling By Invitation

Conditions

  • Hispanic or Latino
  • Pregnancy in Adolescence
  • Rural Health

Eligibility Criteria

Sex
ALL
Age
14 Years - 18 Years
Healthy Volunteers
Accepted

Interventions

  • Healthy futures ("Futuros Saludables") — BEHAVIORAL
    The developed intervention will be delivered in a workshop format by facilitators, over 8 sessions for teens and parent/guardian(s). Feedback on delivery mode (virtual, in-person, or hybrid) during the co-development sessions. If in-person/hybrid is suggested, feedback will be elicited about preferred location (e.g., a local community center, sports club, etc.). Participants will complete sessions, in either Spanish or English depending on participants' preference, using video conference tools. After the delivery of the intervention, facilitators will take field notes and complete a debriefing questionnaire to assess practicality and fidelity. Teens and parent/guardian(s) will complete a 20-minute survey pre-intervention, immediately post-intervention, three-month, six-month, and twelve-month post-intervention. Surveys will assess acceptability and risk behaviors.

Study Details

The study will utilize an exploratory study design, applying formative research methods to inform the development and pilot testing of an unintended teen pregnancy prevention intervention.

Key Dates

Start date
Sep 23, 2022
Status verified
Oct 2025
Primary completion
Jul 31, 2026
Completion
Sep 30, 2027

Study Design

Enrollment
200 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION

Arms

  • Experimental: One arm pilot trial
    The developed intervention will be delivered in a workshop format by facilitators, over 8 sessions for teens and parent/guardian(s). Feedback will be elicited on delivery mode (virtual, in-person, or hybrid) during the co-development sessions. If in-person/hybrid is suggested, feedback will be elicited about preferred location (e.g., a local community center, sports club, etc.). Sessions will be hosted in either Spanish or English depending on participants' preference, using video conference tools. Teens and parent/guardian(s) will complete a 20-minute survey pre-intervention, immediately after the 8 session intervention, three-month post-intervention, six-month post-intervention, and twelve-month post-intervention. Surveys will assess acceptability and risk behaviors. As in the published Cuidate trials, previously used measures will be used to document validity and comparability.

Primary Outcome Measure

A survey analysis of participant degree of acceptance of conducted intervention using a Likert Scale. [ Time Frame: Immediately after intervention ]

Locations (1)

FacilityCityStateZIPSite coordinators
Childrens Mercy Hospital and ClinicsKansas CityMissouri64108-

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By research site
Childrens Mercy Hospital and Clinics· Kansas City, MO

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