NCT00726076

Brief Summary

The purpose of this study is to test a computer program for people with epilepsy. The program was developed to help people with epilepsy improve their self-management skills for taking medications, reducing stress, and sleeping well.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
194

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jul 2008

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2008

Completed
28 days until next milestone

First Submitted

Initial submission to the registry

July 29, 2008

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 31, 2008

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2010

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2010

Completed
Last Updated

December 11, 2013

Status Verified

December 1, 2013

Enrollment Period

2.3 years

First QC Date

July 29, 2008

Last Update Submit

December 10, 2013

Conditions

Keywords

EpilepsyMedicationStressSleepLifestyle Management

Outcome Measures

Primary Outcomes (1)

  • Epilepsy self-management: medication adherence, stress level, and sleep quality

    Baseline- 6 weeks- 12 weeks

Secondary Outcomes (1)

  • Seizure frequency

    Baseline- 6 weeks- 12 weeks

Study Arms (2)

Treatment

EXPERIMENTAL

The Treatment Group received the WebEase Intervention immediately after completing the Baseline Assessment.

Behavioral: WebEase

Control

EXPERIMENTAL

Control Group also received the WebEase Intervention. However, Control Group participants began the Intervention 6 weeks after completing the Baseline Assessment.

Behavioral: WebEase

Interventions

WebEaseBEHAVIORAL

Computer-based epilepsy self-management program The Treatment Group received the WebEase Intervention immediately after completing the Baseline Assessment

Treatment

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Be 18 years of age or older
  • Understand and speak English
  • Have been diagnosed with epilepsy
  • Have been on an antiepileptic medication (AED) for at least 3 months
  • Have access to the internet
  • Be willing to participate
  • Have not participated in WebEase in the past

You may not qualify if:

  • Under age 18
  • Unable to understand and speak English
  • Have NOT been diagnosed with epilepsy
  • Have NOT been on an AED for at least 3 months
  • Not willing to participate
  • Have participated in WebEase in the past

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rollins School of Public Health, Emory University

Atlanta, Georgia, 30322, United States

Location

Related Publications (2)

  • Walker ER, Bamps Y, Burdett A, Rothkopf J, Diiorio C. Social support for self-management behaviors among people with epilepsy: a content analysis of the WebEase program. Epilepsy Behav. 2012 Mar;23(3):285-90. doi: 10.1016/j.yebeh.2012.01.006. Epub 2012 Feb 23.

    PMID: 22364762BACKGROUND
  • DiIorio C, Bamps Y, Walker ER, Escoffery C. Results of a research study evaluating WebEase, an online epilepsy self-management program. Epilepsy Behav. 2011 Nov;22(3):469-74. doi: 10.1016/j.yebeh.2011.07.030. Epub 2011 Sep 1.

MeSH Terms

Conditions

Epilepsy

Condition Hierarchy (Ancestors)

Brain DiseasesCentral Nervous System DiseasesNervous System Diseases

Study Officials

  • Colleen DiIorio, PhD, RN

    Rollins School of Public Health, Emory University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor Emerita

Study Record Dates

First Submitted

July 29, 2008

First Posted

July 31, 2008

Study Start

July 1, 2008

Primary Completion

October 1, 2010

Study Completion

November 1, 2010

Last Updated

December 11, 2013

Record last verified: 2013-12

Locations