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Contraception Perspectives in Adolescents in Haiti

Barriers and Facilitators to Long-Acting Reversible Contraception: Perspectives of Adolescents and Healthcare Providers in Rural Haiti

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05252052
Enrollment
200
Registered
2022-02-23
Start date
2021-03-22
Completion date
2023-07-31
Last updated
2023-08-02

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

Conditions

Contraception

Brief summary

The overall goal of this study is to assess facilitators and barriers to contraception with a focus on long-acting reversible contraception (LARC) among adolescents and health care providers (HCPs) in rural Haiti. The investigator plans to accomplish the following objectives:

Detailed description

Objective 1: Develop locally-informed surveys and in-depth interview guides, based on the ecologically-expanded Theory of Planned Behavior, to assess attitudes, social norms, perceived behavioral control, and intentions regarding contraception, with a focus on LARC, among adolescents and HCPs in rural Haiti. Objective 2: Conduct a formative mixed methods study of attitudes, social norms, perceived behavioral control, and intentions regarding contraception, with a focus on LARC, among female adolescents (N=150 survey, 25-50 in-depth interviews) and HCPs (N=15; survey and in-depth interviews) in rural Haiti.

Interventions

OTHERInterviews/Surveys

This is a cross sectional survey and interviews of adolescents 14- 18 years old and HCPs living in rural Haiti

Sponsors

Children's Mercy Hospital Kansas City
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
14 Years to 24 Years
Healthy volunteers
Yes

Inclusion criteria

• * Adolescents who are biologically female and have reproductive potential (14-24 years old) * Adolescents who reside in the birthing clinic catchment area * Health care providers, including nurse midwives, who work at the local birthing clinic and providers at the local hospital

Exclusion criteria

-Subjects who are determined to have severe psychiatric illness or cognitive impairment (based on research team assessment).

Design outcomes

Primary

MeasureTime frameDescription
Identification of facilitators and barriers to contraception useData collection will occur over one day for individual participants. Study data collection will occur over 18 monthsThe primary outcome is identification of facilitators and barriers to contraception use among adolescent participants based on responses to the eTPB domains described in Table 1. The investigator will also explore facilitators and barriers to contraception use among HCP participants.

Countries

United States

Outcome results

None listed

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