Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03329703 · ClinicalTrials.gov registry record · NA

Project UPLIFT for Psychogenic Non-Epileptic Seizures

A NA study, sponsored by Dartmouth-Hitchcock Medical Center.

Completed
Registry status
NA
Development phase
8
Enrollment target

NCT03329703: Completed NA study, sponsored by Dartmouth-Hitchcock Medical Center.

NCT03329703 is a NA study that has completed, run by Dartmouth-Hitchcock Medical Center. The registered enrollment target is 8 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03329703, a NA study, has completed, sponsored by Dartmouth-Hitchcock Medical Center.

COMPLETED
Registry status
NA
Development phase
8 participants
Enrollment target

Study Summary

Developed by researchers from the Centers for Disease Control and Prevention (CDC), Project UPLIFT (Using Practice and Learning to Increase Favorable Thoughts) is a group telephone program designed to improve depression for people with epilepsy. Project UPLIFT uses evidence-based approaches of cognitive-behavioral therapy (CBT) and mindfulness-based cognitive therapy to help people manage and prevent symptoms of depression. For people with psychogenic non-epileptic seizures, there are few treatment options for depression that address the relationship between mood and seizures. There is evidence that mindfulness-based therapy and cognitive therapy are both effective for people with non-epileptic seizures, both in treating depression and reducing seizure frequency. In this study, Project UPLIFT will be offered to patients with psychogenic non-epileptic seizures. Project UPLIFT is facilitated by a trained clinician to groups of 4-8 patients over the telephone. The group will meet at a regular time, once a week, for 8 consecutive weeks. Participants will be assigned to one of two groups: an immediate-treatment or a waitlist control group which will begin Project UPLIFT 3 months after enrolling in the study.

Primary Outcome

To test the feasibility of giving Project UPLIFT to patients with PNES

Interventions

  • BEHAVIORAL Project UPLIFT

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2018-07-23
Est. Completion 2020-12-31
Phase NA
Dartmouth-Hitchcock Medical Center

427 total trials

What the finished NCT03329703 record still lists

NCT03329703 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which Project UPLIFT is the first listed.

NCT03329703 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03329703 about?

NCT03329703 is a clinical study titled "Project UPLIFT for Psychogenic Non-Epileptic Seizures". Developed by researchers from the Centers for Disease Control and Prevention (CDC), Project UPLIFT (Using Practice and Learning to Increase Favorable Thoughts) is a group telephone program designed to improve depression for people with epilepsy. Project UPLIFT uses evidence-based approaches of cogni...

What is the current status of trial NCT03329703?

This trial is currently completed. It is a NA study. The enrollment target is 8 participants. The study started on 2018-07-23. Estimated completion is 2020-12-31.

What interventions are being tested in trial NCT03329703?

The interventions under investigation include: Project UPLIFT (BEHAVIORAL).

Who is sponsoring clinical trial NCT03329703?

This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 427 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03329703's enrollment target sits among peer trials

8 1976th of 2000 higher than 19 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03329703, the US trial registry maintained by the National Library of Medicine. NCT03329703 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.