Exercise Education for Adults With Seizure Disorders
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|ClinicalTrials.gov Identifier: NCT01856335|
Recruitment Status : Completed
First Posted : May 17, 2013
Last Update Posted : October 8, 2018
-People with seizures benefit from regular exercise. Exercise may help decrease the number of seizures they have. It also improves overall health and quality of life. However, people with seizure disorders often have been prevented from doing sports or other regular physical activity. They may also feel that exercise or injury can increase their risk of seizures. Researchers want to try an exercise program for people who have seizures to see if they can increase motivation to exercise which will improve overall health and may decrease the frequency of seizures.
- To see how exercise education improves motivation to exercise in people who have a history of seizures.
- Individuals at least 18 years of age who have a history of seizures.
- This study involves three outpatient visits and weekly telephone calls for about 12 weeks. There will be followup calls at about 6 and 12 months after the outpatient visits.
- Participants will be screened with a physical exam and medical history. They will answer questions about their current level of physical activity, mood, quality of life, and ideas about exercise.
- At the first visit, participants will learn how to keep a physical activity log and seizure calendar. They will also use an activity monitor and take their pulse regularly. They will complete questionnaires about their mood and thoughts about exercise and seizures.
- At the second visit, participants will set personal activity goals and learn about physical activity and seizures. They will review the physical activity log, seizure log, and activity monitor and pulse readings for the previous 4 weeks.
- After the second visit, participants will receive weekly telephone calls. Each call will last about 5 minutes. These calls will ask about physical activities for the week and participants' progress toward meeting their goals. These calls will also review the seizure log.
- At the third visit (12 weeks), the same tests from the first visit will be repeated.
- The followup phone calls will continue to monitor participants' activity levels.
|Condition or disease||Intervention/treatment||Phase|
|Seizures Epilepsy||Other: Patient Education Other: exercise: increase physical activity/goal setting||Early Phase 1|
To see what keeps people with seizures from exercising and see how they can increase their belief that they can exercise and that exercise will help them.
50 adults with seizures
In this protocol, we will pilot the use of an educational intervention to provide people with seizure disorders an opportunity to learn about the benefits of exercise and learn specifically what types of exercise to incorporate into their daily lives.
To assess the effectiveness of the educational intervention, we will use pre and post intervention measures including seizure specific measures of self-efficacy (belief that they can exercise) and outcome expectations (belief that exercise will help them) for exercise. To assess changes in physical activity, seizure frequency, and mood, we will monitor physical activity and seizure calendars, activity monitor recordings, and mood rating scales.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||30 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Increasing Self-Efficacy and Outcome Expectations For Exercise in Adults With Epilepsy: An Educational Motivation Intervention - E-MOVE|
|Study Start Date :||May 10, 2013|
|Actual Primary Completion Date :||January 25, 2017|
|Actual Study Completion Date :||January 25, 2017|
- Change in Self-efficacy for exercise score following the E-MOVE intervention. [ Time Frame: 0 and 12 weeks post intervention ]
- Change in Outocme Expectations for exercise score following the E-MOVE intervention. [ Time Frame: 0 and 12 weeks post intervention ]
- The effect of the E-MOVE intervention on seizure frequency based on seizure calendar self-report, quality of life scores, symptoms of depression and BMI measures. [ Time Frame: 0 and 12 weeks post intervention ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01856335
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike|
|Bethesda, Maryland, United States, 20892|
|Principal Investigator:||Irene H Dustin, C.R.N.P.||National Institute of Neurological Disorders and Stroke (NINDS)|