Behavioral and Educational Tools to Improve Epilepsy Care
NCT02646631 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32
Last updated 2018-12-24
Summary
The long-term goal of this research is to improve seizure control among patients with epilepsy, which has the potential to improve quality of life for thousands of people living with epilepsy and reduce health care utilization, social and economic costs, and epilepsy-related mortalities. Participants who are suffering from epilepsy will be randomized to receive usual care (UC), a smartphone-based self-management intervention called Management of Risks in Epilepsy (MORE), or MORE + telephone-based motivational interviewing (MI). Participants will be followed for 3 months.
Conditions
Interventions
- OTHER
-
Usual Care
Participants assigned to this treatment will receive the usual care as determined by their physician
- BEHAVIORAL
-
Management of Risks in Epilepsy (MORE)
MORE is a smartphone application which participants use to record information on a daily basis about seizures (severity, type), medications, and mood and stress levels. It also includes a camera-based application which uses a pill scanner and photo to record the identity and quantity (dose) of medications just prior to them being taken. Also included in the app are medication reminders, educational video clips, and self-management tips.
- BEHAVIORAL
-
Telephone-based motivational interviewing (MORE+MI)
Participants will receive a total of 4 motivational interviewing sessions over the phone. These sessions last approximately 20 minutes each and build on the educational materials already provided within the MORE app.
- OTHER
-
Educational Materials
Printed educational materials on the management of epilepsy
Sponsors & Collaborators
-
UCB Pharma
collaborator INDUSTRY - lead OTHER
Principal Investigators
-
Tanya Spruill · New York University Medical School
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-09-30
- Primary Completion
- 2017-11-20
- Completion
- 2017-11-20
Countries
- United States
Study Locations
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