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Recruiting NCT06989086

NCT06989086 FearLess in NeuroOncology

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Clinical Trial Summary
NCT ID NCT06989086
Status Recruiting
Phase
Sponsor Virginia Commonwealth University
Condition Primary Malignant Brain Tumor
Study Type INTERVENTIONAL
Enrollment 112 participants
Start Date 2025-06-24
Primary Completion 2028-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Fearless in Neuro-Oncology

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 112 participants in total. It began in 2025-06-24 with a primary completion date of 2028-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The overarching goal of this project is to assess the feasibility, acceptability, and appropriateness of recruitment methods, target population, and a waitlist design to finalize the protocol of FearLess in primary malignant brain tumor patients and caregivers

Eligibility Criteria

Inclusion Criteria: Patients: * Self-report a diagnosis of a primary malignant brain tumor (grade II-IV) * \>2 weeks post-cranial resection or biopsy * Elevated Fear of Recurrence Distress Rating * Primarily English speaking * \>/= 18 years of age at the time of enrollment Caregivers: * nonprofessional caregiver to a patient with a primary malignant brain tumor (grade II-IV) * Elevated Fear of Recurrence Distress Rating * Primarily English speaking * \>/= 18 years of age at the time of enrollment Exclusion Criteria: Patient / Caregiver Exclusion: * Cognitive impairment that might prohibit active intervention engagement * Inability to understand and provide informed consent * Inability to attend virtual sessions due to unstable or no internet connection

Contact & Investigator

Central Contact

Mary Bridgman

✉ LiveNOW@vcu.edu

📞 804-628-6799

Principal Investigator

Ashlee R Loughan, Ph.D

PRINCIPAL INVESTIGATOR

Virginia Commonwealth University

Frequently Asked Questions

Who can join the NCT06989086 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Primary Malignant Brain Tumor. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06989086 currently recruiting?

Yes, NCT06989086 is actively recruiting participants. Contact the research team at LiveNOW@vcu.edu for enrollment information.

Where is the NCT06989086 trial being conducted?

This trial is being conducted at Richmond, United States.

Who is sponsoring the NCT06989086 clinical trial?

NCT06989086 is sponsored by Virginia Commonwealth University. The principal investigator is Ashlee R Loughan, Ph.D at Virginia Commonwealth University. The trial plans to enroll 112 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology