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Recruiting NCT07087821

NCT07087821 NYU Epilepsy Self-Management Study

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Clinical Trial Summary
NCT ID NCT07087821
Status Recruiting
Phase
Sponsor NYU Langone Health
Condition Epilepsy
Study Type INTERVENTIONAL
Enrollment 108 participants
Start Date 2025-09-16
Primary Completion 2027-09-29

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
UPLIFTPACESEnhanced Usual Care

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 108 participants in total. It began in 2025-09-16 with a primary completion date of 2027-09-29.

⚠ 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 investigators will conduct two-arm randomized controlled trials (RCTs) comparing effects of UPLIFT vs. enhanced usual care and PACES vs. enhanced usual care, respectively, on quality of life, depressive symptoms and seizures over 12 months in NYU patients with epilepsy.

Eligibility Criteria

Inclusion Criteria: * Adults (≥18 years) * English-speaking (UPLIFT and PACES) or Spanish-speaking (UPLIFT only). * Diagnosed with epilepsy for at least one year * Able to understand the informed consent and provide consent * Elevated depressive symptoms - Patient Health Questionnaire-9 (PHQ-9) score ≥10; applies to UPLIFT only Exclusion Criteria: * Severe depressive symptoms (score of ≥20 on PHQ-9) * Active suicidal ideation (score of ≥1 on PHQ-9 item #9 or otherwise reported during screening) * Active psychotic disorder (psychiatric diagnosis and/or antipsychotic medications in the electronic health records (EHR) * Significant cognitive impairment (indicated in the EHR or evident during screening)

Contact & Investigator

Central Contact

Tanya Spruill, PhD

✉ Tanya.Spruill@nyulangone.org

📞 646-501-3429

Principal Investigator

Tanya Spruill, PhD

PRINCIPAL INVESTIGATOR

NYU Langone Health

Frequently Asked Questions

Who can join the NCT07087821 clinical trial?

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

Is NCT07087821 currently recruiting?

Yes, NCT07087821 is actively recruiting participants. Contact the research team at Tanya.Spruill@nyulangone.org for enrollment information.

Where is the NCT07087821 trial being conducted?

This trial is being conducted at Brooklyn, United States, New York, United States.

Who is sponsoring the NCT07087821 clinical trial?

NCT07087821 is sponsored by NYU Langone Health. The principal investigator is Tanya Spruill, PhD at NYU Langone Health. The trial plans to enroll 108 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: July 2026  ·  Data Methodology