Contraception Perspectives in Adolescents in Haiti

Sponsor
Children's Mercy Hospital Kansas City (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05252052
Collaborator
(none)
165
1
23.3
7.1

Study Details

Study Description

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:

Condition or Disease Intervention/Treatment Phase
  • Other: Interviews/Surveys

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
165 participants
Observational Model:
Ecologic or Community
Time Perspective:
Cross-Sectional
Official Title:
Barriers and Facilitators to Long-Acting Reversible Contraception: Perspectives of Adolescents and Healthcare Providers in Rural Haiti
Actual Study Start Date :
Mar 22, 2021
Anticipated Primary Completion Date :
Mar 1, 2023
Anticipated Study Completion Date :
Mar 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Adolescents 14-24 years old

Adolescents 14-24 years old

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

Health care providers in rural Haiti

Health care providers in rural Haiti

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

Outcome Measures

Primary Outcome Measures

  1. Identification of facilitators and barriers to contraception use [Data collection will occur over one day for individual participants. Study data collection will occur over 18 months]

    The 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years to 24 Years
Sexes Eligible for Study:
Female
Accepts 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).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Children's Mercy Hospital Kansas City Missouri United States 64108

Sponsors and Collaborators

  • Children's Mercy Hospital Kansas City

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Abbey Masonbrink, Pediatric Hospitalist, Children's Mercy Hospital Kansas City
ClinicalTrials.gov Identifier:
NCT05252052
Other Study ID Numbers:
  • STUDY00001626
First Posted:
Feb 23, 2022
Last Update Posted:
Feb 23, 2022
Last Verified:
Jan 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Feb 23, 2022