Mode
Text Size
Log in / Sign up
N/A N=30 Randomized Single-blind Supportive Care

EMR Outcomes: Anxiety and Depression in Epilepsy

Quality of Life · Anxiety · Depression · Epilepsy

Enrolled (actual)
30
Serious AEs
6.7%
Results posted
Jan 2022
Primary outcome: Primary: Percentage of Participants Retained in the Study in the EMR Arm — 67 percentage of participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
EMR-based-interventional method (Other); Telephone-based-standard method (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Wake Forest University Health Sciences
Primary completion
Nov 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants Retained in the Study in the EMR Arm
67
SECONDARY
Percentage of Participants Retained in the Study in the Phone Arm
100
SECONDARY
Quality of Life in Epilepsy-10 (QOLIE-10)
57.6; 62.6
SECONDARY
Quality of Life in Epilepsy-10 (QOLIE-10)
57.6; 62.6
SECONDARY
Quality of Life in Epilepsy-10 (QOLIE-10)
57.6; 62.6
SECONDARY
Generalized Anxiety Disorder 7-item (GAD-7) Scale
7.7; 8.5
SECONDARY
Generalized Anxiety Disorder 7-item (GAD-7) Scale
7.7; 8.5
SECONDARY
Generalized Anxiety Disorder 7-item (GAD-7) Scale
7.7; 8.5
SECONDARY
Neurological Disorders Depression Inventory (NDDI-E)
14.7; 13.8
SECONDARY
Neurological Disorders Depression Inventory (NDDI-E)
14.7; 13.8
SECONDARY
Neurological Disorders Depression Inventory (NDDI-E)
14.7; 13.8

Summary

The purpose of this research is to find out how people with epilepsy and possible symptoms of anxiety or depression are doing for 6 months after a regular epilepsy clinic visit. Participants in this study will complete questionnaires either by phone or via the patient portal.

Eligibility Criteria

Inclusion Criteria

  • Age 18 or older
  • Completed electronic questionnaires independently in clinic
  • Epilepsy diagnosis (clinician impression or EEG-based)
  • Borderline or high anxiety or depression symptoms at baseline
  • GAD-7 score > 7 (anxiety)
  • NDDI-E score > 13 (depression)

Exclusion Criteria

  • Passive suicidal ideation (NDDI-E item 4 score of 3 or 4)
  • Age <18 years
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03879525). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search