Baltimore, MDNCT07064837Now EnrollingIRB Ready

Contraceptive Use Clinical Trial in Baltimore, MD

Access cutting-edge contraceptive use treatment through this clinical trial at a research site in Baltimore. Study-provided care at no cost to qualified participants.

Sponsored by Johns Hopkins University

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Expert Care in Baltimore

Access contraceptive use specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related contraceptive use treatment provided free

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Check if you qualify for this contraceptive use clinical trial in Baltimore, MD

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Baltimore

    Convenient for MD residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Baltimore site if eligible
  4. 4Begin participation

About This Contraceptive Use Study in Baltimore

The purpose of this study is to understand in what ways the pediatrician's office can support women's family planning by screening for contraceptive needs at each well child visit over the first 12 months of the child's life. Part one of the study will be working with families and clinic-based social needs navigators around where and how the screening process will be integrated into an existing pediatric workflow. Part two of the study will include (a) surveying mothers of 12-15 month olds about contraceptive use experience to get a baseline followed by (b) implementing the screening process into pediatrics and measuring how well the screener is able to identify unmet contraceptive needs and how people are or are not using the screening process. This will occur over approximately 12 months. Part (b) includes enrolling families who have a contraceptive need case and following the case in the child's medical record. At the end of the 12 month intervention the investigators will (c) invite some families to participant in an interview about the experience with the contraceptive need screener. Part three will be focus group feedback from clinicians and staff about the contraceptive need screening process. Part four will be key informant interviews with community stakeholders on the expansion of this screener.

Sponsor: Johns Hopkins University

Who Can Participate

Inclusion Criteria

individuals who identify as Latina AND foreign-born, AND
communication preference is Spanish AND
22 years or older (any parent 21 years or younger is almost always also one of the investigator's patients) AND
are the biological parent of a 12 month old child who is a BMS patient. Intervention cohort inclusion criteria are:
individuals who identify as Latina AND foreign-born, AND
communication preference is Spanish AND
22 years or older AND
are the biological parent of a \< 1 month old who is a BMS patient. Participant inclusion criteria for Both:
BMS staff OR Hopkins Community Connection Advocate staff AND
age 18 years or older. Participant inclusion criteria for semi-structured interviews:
Member of intervention cohort group AND child
has completed 12 months of life AND
has completed contraceptive need survey. Participant inclusion criteria for key informant interviews:
staff member from one of 5 local health care clinics including Baltimore City Department of Health, Planned Parenthood, Women, Infants, and Children, and two federally qualified health centers AND
direct interaction with Spanish speaking individuals AND
age 18 years or older.

Exclusion Criteria

Individuals with bilateral tubal ligation (permanent contraception) at time of recruitment

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Baltimore?

Yes, this clinical trial (NCT07064837) has an active research site in Baltimore, MD that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Contraceptive Use Treatment Options in Baltimore, MD

If you're searching for contraceptive use treatment options in Baltimore, MD, this clinical trial (NCT07064837) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Baltimore research site is actively enrolling participants for this clinical trial. You'll receive care from experienced contraceptive use specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all contraceptive use clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Baltimore, MD