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Yoga and Aerobic Exercise in Epilepsy

Investigation of the Effects of Yoga and Aerobic Exercise Training on Physical and Mental Health in People With Epilepsy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05066880
Enrollment
60
Registered
2021-10-04
Start date
2021-10-07
Completion date
2024-05-01
Last updated
2024-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epilepsy, Epilepsy Idiopathic, Epilepsy; Seizure

Keywords

epilepsy, yoga, aerobic, exercise

Brief summary

In recent years, there is growing interest in illustrating the health benefits of exercise among epilepsy. Although exercise is recommended for patients with epilepsy, there is uncertainty concerning the effects of yoga and aerobic exercise on multiple health outcomes in epilepsy. The aim of this trial is to examine the effects of yoga and aerobic exercise training on physical activity, health-related physical fitness, mental, emotional, and psychological health status, seizure frequency and quality of life.

Interventions

OTHERExercise training

Exercise training for 8 weeks

Sponsors

Dokuz Eylul University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients with epilepsy diagnosed by a neurologist using the International League Against Epilepsy (ILAE) criteria, * Having access to the internet at least three per week.

Exclusion criteria

* Any history of neurological disorders other than epilepsy, * Significant physical and cognitive impairments, * Musculoskeletal comorbid conditions, * Contraindications for an exercise intervention including diagnosed cardiovascular, pulmonary, or endocrine diseases, * Pregnancy, * Mental deficiency or low education level to understand the questionnaires, * Currently participating in an exercise program, * Volunteers who miss 3 consecutive intervention sessions, and do not participate in 10% of sessions.

Design outcomes

Primary

MeasureTime frameDescription
Physical activity in daily lifechange from baseline to 8 weeksPhysical activity will be objectively monitored with an accelerometer.
Seizurechange from baseline to 8 weeksParticipants will be given a seizure diary and requested to record the number of their seizure.

Secondary

MeasureTime frameDescription
30-second Chair Stand testchange from baseline to 8 weeksLower body strength will be determined using the 30-second Chair Stand test.
Bioelectrical impedance analyzerchange from baseline to 8 weeksBody composition measurements will be performed with bioelectrical impedance analyzer.
Waist and hip circumferencechange from baseline to 8 weeksFor the anthropometric measurements, waist and hip circumference will be taken.
Trail Making test and Digit Span testchange from baseline to 8 weeksThe Trail Making test and Digit Span test will be used to evaluate for attention.
Stroop test and Verbal Fluencychange from baseline to 8 weeksThe Stroop test and Verbal Fluency will be used to evaluate for executive functions.
Weschler Memory Scale-Revised Visual Reproduction subtestchange from baseline to 8 weeksThe Weschler Memory Scale-Revised Visual Reproduction subtest will be used to evaluate for visual memory.
Clock Drawing testchange from baseline to 8 weeksThe Clock Drawing test will be used to evaluate for visual perception and visual-spatial functions.
Biodex Balance Systemchange from baseline to 8 weeksBalance evaluation will be performed with Biodex Balance System.
Neurological Disorders Depression Inventory for Epilepsychange from baseline to 8 weeksThe Neurological Disorders Depression Inventory for Epilepsy will be used to evaluate for depression.
Generalized Anxiety Disorder-7change from baseline to 8 weeksAnxiety will be determined by the Generalized Anxiety Disorder-7.
10-item Perceived Stress Scalechange from baseline to 8 weeksThe 10-item Perceived Stress Scale will be used to assess subjective stress.
Fatigue Impact Scalechange from baseline to 8 weeksFatigue will be assessed with the Fatigue Impact Scale.
Pittsburg Sleep Quality Indexchange from baseline to 8 weeksSleep quality will be measured using the Pittsburg Sleep Quality Index.
Quality of Life in Epilepsy Inventory-31change from baseline to 8 weeksIt will be used to determine health-related quality of life for epilepsy.
Oktem Verbal Memory Processes testchange from baseline to 8 weeksThe Oktem Verbal Memory Processes test will be used to evaluate for verbal memory performance.
Six-Minute Walk testchange from baseline to 8 weeksThe Six-Minute Walk test will be used to determine functional capacity.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026