Can a virtual coaching program help teens with epilepsy master laundry and cooking?
NCT ID NCT07676539
First seen Jun 30, 2026 · Last updated Jul 09, 2026 · Updated 3 times
Summary
This pilot trial tests a 15-week telehealth program called Surviving and Thriving in the Real World (STRW) for teens aged 14–18 with epilepsy who struggle with daily living skills. The program includes weekly caregiver-teen sessions and separate caregiver group meetings, all delivered online. Researchers want to see if the program is acceptable and helpful for improving skills like cooking, laundry, and money management.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Surviving and Thriving in the Real World (STRW) behavioral program
- What this could lead to
- If successful, this program could offer a practical way to help teens with epilepsy gain independence in daily tasks.
- What could go wrong
- This is a very small pilot study with only 8 participants, so results may not apply to everyone. The program requires a significant time commitment from families.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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8 people
The number who actually took part.
- Started
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Dec 2025
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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14 to 19 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. diagnosed with epilepsy at least 1 year ago, 2. enrolled in 9th-12th grade (i.e., 14-18 years old at time of enrollment) 3. deficits in adaptive functioning per caregiver report (i.e., standard score below 90 on either the ABAS-3 Practical Domain or General Adaptive Composite \[GAC\]), 4. not planning to wean off anti-seizure medication (ASM) within the intervention timeframe, 5. and family's primary language is English. Exclusion Criteria: 1. Parent- or clinician-reported history in the adolescent/young adult of: 1. history of developmental delay (e.g., autism spectrum disorder, pervasive development disorder, history of services for developmental delay or intellectual impairment in the past 5 years, known IQ\<70), 2. severe mental illness (e.g., schizophrenia, bipolar disorder, eating disorder within the past 12 months), 3. currently on the ketogenic diet, 4. and history of epilepsy surgery in the past year. 2. Clinician-reported diagnosis in the adolescent/young adult of: 1. one or more episodes of status epilepticus within the 24 weeks prior to enrollment 2. treatable causes of seizures (for example, identified etiologies including metabolic, neoplastic or active infectious origin), 3. a confirmed or suspected epileptic encephalopathy (e.g., electrical status epilepticus in sleep, Landau Kleffner syndrome, West syndrome), 4. a confirmed or suspected progressive and degenerative disorder (e.g., mitochondrial disorders, metabolic disorders, autoimmune disorders), 5. non-epileptic events/seizures.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229, United States
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Other studies related to the condition(s) this trial covers.
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