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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02925663
Other study ID # R21HD083335
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date October 10, 2016
Est. completion date June 28, 2018

Study information

Verified date July 2018
Source Children's Hospital Medical Center, Cincinnati
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to establish the feasibility, accessibility, acceptability, and preliminary efficacy of an individually-tailored intervention to improve EF in adolescents with epilepsy (EFI-E).


Description:

Epilepsy is a common childhood condition affecting approximately 326,000 youth in the United States. Adolescents with epilepsy are at significant risk for poor social and academic outcomes, neurobehavioral comorbidities (i.e., internalizing and externalizing symptoms), and poor treatment adherence. Studies have shown that one potential reason for these poor outcomes are deficits in executive functioning (EF), defined as the skills necessary for goal-directed and complex activities, including problem-solving, initiation, monitoring, organization, planning, self-regulation and working memory. EF deficits have been documented in 1/3 of youth with epilepsy, which is 3 times the prevalence in healthy youth. Evidence-based interventions to improve EF could play a critical role in preventing adverse outcomes (e.g., psychological comorbidities, non-adherence to the treatment regimen) and promoting optimal functioning in adolescents with epilepsy; however none exists for this vulnerable population. The aim of the current study is to establish the feasibility, accessibility, acceptability, and preliminary effects of an individually-tailored intervention to improve EF in adolescents with epilepsy (Executive Functioning Intervention-Epilepsy; EFI-E). Thirty participants will be recruited who have at least one clinically-elevated EF subscale or at least two at-risk subscale scores (> 1 standard deviation above the mean) on the parent Behavior Rating Inventory of Executive Function (BRIEF®)) to qualify for the EFI-E. EFI-E will consist of 10 web-based modules addressing foundational EF skills. Each online module will be accompanied by a videoconference with a therapist to review the skills and problem solve around adolescent-identified goals. Baseline and post-treatment questionnaires will be completed by adolescents and primary caregivers and electronically-monitored adherence will be obtained throughout the open trial. Participants will be in the trial for 9 months.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date June 28, 2018
Est. primary completion date January 4, 2018
Accepts healthy volunteers No
Gender All
Age group 13 Years to 17 Years
Eligibility Inclusion criteria

- Age 13-17 years

- Diagnosis of epilepsy

- Have at least two subclinical (>1 SD; T score between 60-65) or one clinically-elevated BRIEF subscale (T score > 65)

- Primary caregiver consent and adolescent assent to participate in study

Exclusion criteria

- Diagnosis of non-epilepsy medical disorders requiring daily medications with the exception of asthma and/or allergies

- Diagnosis of significant developmental disorders (e.g. Autism)

- Inability to read and speak English due to the questionnaires and intervention only been developed in English

- Family lives greater than 100 miles away from CCHMC

- If patient is planning to wean from their antiepileptic medication within the next 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
EFI-E
This is 10 web-based modules addressing foundational EF skills. Each online module will be accompanied by a videoconference with a therapist to review the skills and problem solve around adolescent-identified goals.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Children's Hospital Medical Center, Cincinnati

Outcome

Type Measure Description Time frame Safety issue
Other Child behavioral and emotional functioning: Behavior Assessment Schedule for Children-2 3-months
Other Treatment Feasibility Treatment Feasibility and Acceptability Questionnaire 3-months
Other Executive functioning-BRIEF 5-months
Other Executive functioning-BRIEF 8-months
Other Adherence-SImple Med Pillbox or MEMS TrackCaps 8-months
Primary Executive functioning: Behavior Rating Inventory of Executive Function (BRIEF) 3-months
Secondary Adherence: SimpleMed Pillboxes or MEMS TrackCaps 3-months
Secondary Quality of life: PedsQL Epilepsy Module 3-months
Secondary Seizures A combination of chart review and parent-report will be used to create a composite seizure presence/absence variable. 3-months
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