Clinical trial Recruiting at 1 site Observational Ages 18 and up

Meningioma: How social factors and personal risks relate to health outcomes

Official title: An Investigation of Tumor Genomics, Individual Risk Factors, and External Drivers of Health to Improve Health Outcomes for Patients With Meningioma

Run by University of California, San Francisco · NCT07418775 · Data updated 2026-11-12

This study tests whether social and personal risk factors help explain differences in health outcomes for adults with meningioma.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment3000 (estimated)
SponsorUniversity of California, San Francisco
Academic / other
Locations1 site (San Francisco, California)
StatusRecruiting
StartedJanuary 16, 2026
Main results expectedJanuary 1, 2031
Study endsJanuary 1, 2032
Registry record updatedMay 19, 2026
Trial IDNCT07418775 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 and older with a diagnosed meningioma who can read and speak English and can provide consent.

Probably not a fit

Patients who do not identify with the studied social determinants of health factors or whose conditions do not relate to the topics surveyed may see no direct benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study collects survey data from adults with meningioma and reviews their medical records to explore how social determinants of health and individual risk factors are distributed and may relate to outcomes. Researchers will examine disparities across racial groups and how factors such as access to care, environment, and personal health history correlate with disease experience. The study does not involve an intervention and uses surveys alongside medical record reviews to identify patterns and potential inequities. Participants are adults 18 years or older who can read English and have a meningioma. The lead sponsor is UCSF, with collaboration from the NCI, and the study is conducted at UCSF in San Francisco.

Why it matters

Potential benefit: Findings could illuminate inequities and inform strategies to improve care for diverse meningioma patients.

How similar studies have gone: Previous observational work on health disparities has demonstrated useful insights, though this exact combination of SSDH and meningioma is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults ≥18 years of age
* Able to speak and read English
* Diagnosed with a meningioma

Exclusion Criteria:

* Active psychiatric issues (suicidality, active psychosis, grave disability, etc.)
* Inability to consent secondary to severe neurologic deficit or psychiatric distress
* Inability to complete survey secondary to severe neurologic deficit or psychiatric distress

Where it's running

  • University of California San Francisco
    San Francisco, California, United States
    Recruiting

Study contacts

  • Principal investigator: David Raleigh, MD, PhD — University of California, San Francisco, San Francisco, California 94143
  • Study coordinator: Zora Arum
  • Email: zora.arum2@ucsf.edu
  • Phone: 877-827-3222

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.