Houston, TXNCT06843720Now EnrollingIRB Ready

HR-HPV Testing Clinical Trial in Houston, TX

Access cutting-edge hr-hpv testing treatment through this clinical trial at a research site in Houston. Study-provided care at no cost to qualified participants.

Sponsored by M.D. Anderson Cancer Center

Quick Self-Assessment

See if you qualify for this Houston location

Preparing your pre-screening questions…

Expert Care in Houston

Access hr-hpv testing specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related hr-hpv testing treatment provided free

Apply for This Houston Location

Check if you qualify for this hr-hpv testing clinical trial in Houston, TX

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Houston

    Convenient for TX 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 Houston site if eligible
  4. 4Begin participation

About This HR-HPV Testing Study in Houston

To learn about the attitudes toward implementing self-collection among healthcare providers and staff, participants, and other stakeholders; and to inform the development of patient education and provider training materials to aid in the implementation of self-collection in clinical settings.

Sponsor: M.D. Anderson Cancer Center

Who Can Participate

Inclusion Criteria

Populations involved in the research are:
stakeholder advisory board members;
patients eligible for cervical cancer screening participating in the cluster randomized stepped-wedge trial;
patients and community members participating in formative research activities;
providers, clinic staff, and other health system stakeholders from partnering health systems;
Project ECHO Participants (providers, clinic staff, and other health system stakeholders from partner and non-partner institutions);
Other Clinical Networks (providers, clinic staff and other health system stakeholders from partner and non-partner institutions) The eligibility criteria for each are: Patients eligible for cervical cancer screening:
Currently a resident in the state of Texas
Attend for care at a partner clinic enrolled in the study
Women and persons with a cervix
Due or past due for cervical cancer screening Patients and community members participating in formative research activities: • Purposively identified as a stakeholder for formative research by research staff Providers, clinic staff, and other health system stakeholders from partnering health systems:
Employed at least part-time by a partnering health system
Age 18+ Project ECHO Participants:
Participate in at least one Project ECHO session
Age 18+ Other Clinical Networks:
Participate in at least one clinical network session

Exclusion Criteria

Patients eligible for cervical cancer screening:
Report being currently pregnant
History of total hysterectomy
History of cervical cancer Other study populations: • Unable to communicate in English or Spanish Vulnerable Populations Participants/samples belonging to vulnerable populations (children, pregnant women, cognitively impaired adults, or prisoners) will be prohibited from participation.

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 Houston?

Yes, this clinical trial (NCT06843720) has an active research site in Houston, TX 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.

HR-HPV Testing Treatment Options in Houston, TX

If you're searching for hr-hpv testing treatment options in Houston, TX, this clinical trial (NCT06843720) 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 Houston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced hr-hpv testing 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.

Ready to Join in Houston?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Houston, TX