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Hematopoietic and Lymphatic System NeoplasmNCT07215039

Improving Prison Health Equity Through Cancer Literacy and Screening Awareness in Florida

An observational study of Hematopoietic and Lymphatic System Neoplasm and Malignant Solid Neoplasm, run by Mayo Clinic at 1 site in United States.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

This study evaluates cancer screening awareness, personal and family cancer history, and barriers to screening among incarcerated women at Gadsden Correctional Facility. The information will be used to inform the content of a tailored digital educational module on screenable types of cancer, their risk factors, and… Read more about this study

Who is it for?
Ages 18 years and older, women onlyHealthy volunteers can take part
What is being tested?
Survey
How many people
1,200 participants
Where
1 siteUnited States
Study dates
10 Nov 2025to 30 Oct 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Women currently incarcerated at Gadsden Correctional Facility

Who may be able to join

  • Women aged 18+ currently incarcerated at Gadsden Correctional Facility
  • Pregnant participants are allowed

Who cannot join

  • Women under 18 or not incarcerated

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United States1 site
  • Mayo Clinic in Florida

    Jacksonville, Florida, 32224-9980

Other trials in United States

About this study

This study evaluates cancer screening awareness, personal and family cancer history, and barriers to screening among incarcerated women at Gadsden Correctional Facility. The information will be used to inform the content of a tailored digital educational module on screenable types of cancer, their risk factors, and current screening guidelines that will be disseminated to US prisons and incorporated into release programs and general health literacy programs.

Being tested
Survey

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • SurveyOther

    Non-interventional study

Study groups in NCT07215039
Study groupRoleWhat they receive
ObservationalParticipants complete a survey on study.
Receives: Other: Survey

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Self-reported cancer screening history

    Assessed as the proportion of incarcerated women who meet national cancer screening guidelines based on self-reported screening history. Participants will complete a 4-page, paper-based, anonymous survey that should take approximately 15 minutes to complete. The survey consists of mainly yes/no questions with a few multiple choice and open-ended questions. This is a qualitative survey used to record basic demographic information, cancer knowledge, risk factors, screening history, and adherence to preventive cancer care. Survey results will be used to inform the content of a tailored digital educational module on screenable types of cancer, their risk factors, and current screening guidelines.

    Measured: Baseline (completion of survey)

Secondary outcomes (4)
  1. Awareness of cancer risk factors

    Participants will complete a 4-page, paper-based, anonymous survey that should take approximately 15 minutes to complete. The survey consists of mainly yes/no questions with a few multiple choice and open-ended questions. This is a qualitative survey used to record basic demographic information, cancer knowledge, risk factors, screening history, and adherence to preventive cancer care. Survey results will be used to inform the content of a tailored digital educational module on screenable types of cancer, their risk factors, and current screening guidelines.

    Measured: Baseline (completion of survey)

  2. Awareness of cancer screening guidelines

    Participants will complete a 4-page, paper-based, anonymous survey that should take approximately 15 minutes to complete. The survey consists of mainly yes/no questions with a few multiple choice and open-ended questions. This is a qualitative survey used to record basic demographic information, cancer knowledge, risk factors, screening history, and adherence to preventive cancer care. Survey results will be used to inform the content of a tailored digital educational module on screenable types of cancer, their risk factors, and current screening guidelines.

    Measured: Baseline (completion of survey)

  3. Barriers to cancer screening within correctional settings

    Participants will complete a 4-page, paper-based, anonymous survey that should take approximately 15 minutes to complete. The survey consists of mainly yes/no questions with a few multiple choice and open-ended questions. This is a qualitative survey used to record basic demographic information, cancer knowledge, risk factors, screening history, and adherence to preventive cancer care. Survey results will be used to inform the content of a tailored digital educational module on screenable types of cancer, their risk factors, and current screening guidelines.

    Measured: Baseline (completion of survey)

  4. Barriers to cancer screening follow-up within correctional settings

    Participants will complete a 4-page, paper-based, anonymous survey that should take approximately 15 minutes to complete. The survey consists of mainly yes/no questions with a few multiple choice and open-ended questions. This is a qualitative survey used to record basic demographic information, cancer knowledge, risk factors, screening history, and adherence to preventive cancer care. Survey results will be used to inform the content of a tailored digital educational module on screenable types of cancer, their risk factors, and current screening guidelines.

    Measured: Baseline (completion of survey)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Oct 2025
  2. Study start10 Nov 2025
  3. Primary completion30 Oct 2027 (estimated)
  4. Study completion30 Oct 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Cross-sectional
Enrolment
1,200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07215039
Sponsor's protocol ID
MC250903
Other IDs
NCI-2025-05529, 25-003194
Status last verified
Apr 2026
First submitted
8 Oct 2025
Last updated
17 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Hematopoietic and Lymphatic System Neoplasm and Malignant Solid Neoplasm, run by Mayo Clinic at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 17 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Self-reported cancer screening history (time frame: Baseline (completion of survey)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Apr 2026; AzTrials last refreshed its copy on 8 Nov 2026.

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