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Evaluating the Impact of CHOICE-AYA on Contraceptive Use, Continuation and Satisfaction

A Prospective, Quasi-experimental Study to Evaluate the Feasibility of CHOICE-AYA for Unintended Pregnancy Prevention in Adolescents and Young Adults (AYA) Experiencing Homelessness.

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05022134
Acronym
CHOICE-AYA
Enrollment
200
Registered
2021-08-26
Start date
2022-03-29
Completion date
2027-08-30
Last updated
2026-02-17

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

Conditions

Contraception Behavior, Reproductive Behavior, Sexual Behavior

Keywords

Adolescent, Contraception

Brief summary

This is a prospective study involving two phases: 1) adaptation and 2) intervention, in adolescents aged 14-21 experiencing homelessness. The overarching goal is to develop and evaluate the effectiveness and feasibility of a counselling intervention to improve access to contraception among AYA experiencing homelessness. During the first phase, referred to as the adaption phase, we will rely on collective input from formative groups of AYA experiencing homelessness to adapt the CHOICE counselling intervention for this underserved and under-resourced population. In the second phase, referred to as the intervention phase, we will evaluate the effectiveness and feasibility of the adapted intervention (CHOICE-AYA).

Detailed description

This study will adapt an evidence-based contraceptive counseling intervention (CHOICE) using input from the formative groups of AYA experiencing homelessness and study the impact of the adapted counseling (CHOICE-AYA) on contraceptive use, continuation, and satisfaction in a specialized community care setting. After informed consent is obtained, participants will receive the CHOICE-AYA counseling intervention by trained clinic staff. Provision of contraception based on participant choice will occur through the clinic provider same day. Participants will be sent links to complete the follow-up surveys at 1, 3, 6, and 12 months. In addition, Clinic staff (e.g., prescribers and nurses) will be sent electronic surveys following randomly selected study visits. Findings will inform best practices for this vulnerable population and provide foundational evidence for future studies focused on expanding care to other sites that serve this group.

Interventions

BEHAVIORALCHOICE-AYA

Adapted contraceptive counseling specific to AYA experiencing homelessness

Sponsors

Children's Mercy Hospital Kansas City
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
14 Years to 21 Years
Healthy volunteers
Yes

Inclusion criteria

* Adolescents and young adults experiencing homelessness and housing instability (defined as those seeking care at our community-based clinic on the campus of a youth shelter) aged 14-21 who have female reproductive organs (In Missouri, youth aged ≤13 are not legally able to consent to sex) * English speaking * Prior sexual activity or anticipated future sexual activity that creates the risk of pregnancy * Either not currently on hormonal contraception OR interested in switching methods

Exclusion criteria

* AYA currently seeking pregnancy in the next 3 months * AYA with a severe developmental or cognitive delay that interferes with the ability to engage in consensual reproductive sex (determined by the investigator)

Design outcomes

Primary

MeasureTime frameDescription
Contraceptive uptakeStudy Day 1Rates of reliable contraceptive use

Secondary

MeasureTime frameDescription
Contraceptive satisfaction1, 3, 6, and 12 months post interventionbrief likert-style survey assessing whether they are still on the method, how satisfied they are with this method
Contraceptive continuation1, 3, 6, and 12 months post interventionbrief survey
Feasibility of intervention (perceived by clinic staff and participants)Post-visitBrief survey based on Bowen's constructs of feasibility

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026