跳至主要内容
临床试验/NCT06608966
NCT06608966招募中不适用

Epilepsy Journey 2.0: An Intervention to Improve Executive Functioning in Adolescents With Epilepsy

Children's Hospital Medical Center, Cincinnati6 个研究点 分布在 1 个国家目标入组 310 人开始时间: 2024年11月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
310
试验地点
6
主要终点
Behavior Rating Inventory of Executive Function (2nd edition) Global Executive Composite T-score (parent)

研究概览

简要总结

The goal of this multi-site clinical trial is to determine the effectiveness of two components of a web-based intervention (Epilepsy Journey) to improve executive functioning in adolescents with epilepsy. The two components include web-based modules and problem-solving telehealth sessions with a therapist focused on executive functioning. This trial aims to answer the following questions:

  1. Which components of Epilepsy Journey (web-based modules or telehealth sessions with a therapist) are essential for improving executive functioning in adolescents with epilepsy?
  2. Which components of Epilepsy Journey (web-based modules or telehealth sessions with a therapist) are essential for improving quality of life in adolescents with epilepsy?

Participants will be randomly assigned to one of four groups: 1) Epilepsy Journey web-based modules and telehealth sessions, 2) Epilepsy Journey web-based modules only, 3) telehealth sessions with a therapist only, or 4) treatment as usual.

Participants will:

  • Independently review Epilepsy Journey web-based modules focused on executive functioning skills (~15-30 minutes) and/or have weekly telehealth sessions (~30-45 minutes) with a therapist for 14 weeks.
  • Complete measures of executive functioning (parent and teen-report) and quality of life (teen-report) at the start of the study, 14-, 26-, and 66- weeks after randomization. The NIH toolbox will be completed at the start of the study and 26-weeks after randomization. Additional measures will also be collected.

详细描述

Epilepsy is a common pediatric neurological condition affecting ~470,000 youth in the United States. Adolescents with epilepsy are at significant risk for neurobehavioral comorbidities (i.e., depressive/behavioral symptoms) and suboptimal social, academic, and quality of life outcomes. Research suggests that 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, contribute to suboptimal functioning. EF deficits have been documented in up to 50% 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 and promoting optimal functioning in adolescents with epilepsy; however none exists for this vulnerable population. To fill this gap, the investigators successfully developed and tested Epilepsy Journey (EJ), a comprehensive e-health behavioral multi-component problem-solving intervention that combines 10 self-guided learning modules with 10 telehealth sessions. The promising proof-of-concept trial (n=39) showed high feasibility, acceptability, patient satisfaction, and significant improvements in parent-reported EF behaviors, neurobehavioral functioning, and quality of life. The next logical phase of this research is to conduct a definitive randomized clinical trial to examine: whether the two components of treatment (EJ modules and telehealth) are 1) both essential and 2) have a durable impact on improving parent-reported and performance-based EF behaviors and quality of life. Thus, the aim of the current proposal is to conduct a multi-site Phase 3 randomized controlled clinical trial (RCT) using a 2x2 factorial design to examine the efficacy of separate (EJ modules and EJ telehealth) and combined components of EJ on EF. Participants positive for EF deficits (n=232) will be randomized to one of four arms: 1) EJ modules with telehealth sessions, 2) EJ modules alone, 3) EJ telehealth sessions alone, or 4) Usual Care (no EJ modules or telehealth sessions). Treatment participants will either independently review EJ modules focused on EF skills (~15-30 min.) and/or have weekly telehealth sessions (~30-45 min.) with a therapist for 14-weeks. The groups will learn and apply problem-solving strategies to their individual EF difficulties. Participants will complete measures at baseline, 14-, 26-, and 66- weeks after randomization to examine maintenance of effects. There is a critical need for evidence-based interventions to improve executive functioning behaviors in youth with epilepsy. If the aims of this study are achieved, we will have definitive evidence for addressing EF deficits. The investigators expect that EJ modules and EJ telehealth will demonstrate efficacy alone and in combination, which will allow patients to select the approach best suited to their specific situation. Consequently, we can improve long-term outcomes (e.g., neurobehavioral comorbidities, academic success, social relationships, and quality of life) in adolescents with epilepsy, a high-risk population.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

盲法说明

The PI of the study is masked to treatment condition. Outcome assessors for the NIH toolbox measure will also be masked.

入排标准

年龄范围
13 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Age between 13-17 years at the time of enrollment
  • Child lives at home with primary caregiver and is enrolled in school (excluding summer breaks).
  • Confirmed diagnosis of epilepsy with seizures that are categorized as either generalized or focal in onset. Epilepsy is defined as: 1) At least two unprovoked seizures occurring more than 24-hours apart; or 2) One unprovoked seizure and a probability of further seizures similar to the general recurrence risk after two unprovoked seizures.
  • Primary language of English
  • Screening Inclusion: On the parent-reported Behavior Rating Inventory of Executive Function-2nd edition (BRIEF-2), have executive functioning deficits defined as at least 2 subclinical (60<T<65) or one clinical BRIEF-2 subscale T scores (T≥65).
  • Parent/legal guardian(s) willing to sign an IRB approved informed consent
  • Participant willing to sign an Institutional Review Board approved assent

排除标准

  • Parent or clinician-reported history in the adolescent 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)
  • severe mental illness (e.g., schizophrenia, bipolar disorder, eating disorder within the past 12 months, depression with active suicidal ideation or suicidal ideation/intent in the past 3 months)
  • prior (3-months) or current history of trauma and/or stressor-related disorders (e.g. PTSD)
  • recent or current significant medical disease (i.e., cardiovascular, hepatic, renal, gynecologic, musculoskeletal, metabolic or endocrine)
  • brain injury or brain tumor; and/or
  • epilepsy surgery
  • any other medical and/or psychological condition that takes treatment precedence over the study intervention
  • Clinician-reported diagnosis in the adolescent of
  • epilepsy whose seizures are categorized only as either unknown onset or unclassified onset (defined as insufficient information to determine onset)
  • epilepsy currently being treated at the time of enrollment by 3 or more antiseizure medications (ASMs) (excluding rescue medication use)
  • epilepsy with a history of failure to achieve seizure freedom despite adequate use of 4 different anti-seizure medications
  • a confirmed or suspected epileptic encephalopathy (e.g., electrical status epilepticus in sleep, Landau Kleffner syndrome, West syndrome)
  • a confirmed or suspected progressive and degenerative disorder (e.g., mitochondrial disorders, metabolic disorders, autoimmune disorders)
  • one or more episodes of status epilepticus within the 24 weeks prior to enrollment; and/or
  • treatable causes of seizures, for example identified etiologies including metabolic, neoplastic, or active infectious origin.
  • non-epileptic event/seizures
  • Adolescents currently on the ketogenic diet
  • Participation in a trial of an investigational drug or device within 30 days prior to screening

研究组 & 干预措施

Epilepsy Journey web-based modules alone

Experimental

Participants assigned to Epilepsy Journey modules will independently review web-based EJ modules. Participants will be targeted to complete 10 EJ modules (~15-30 minutes each session) within 14 weeks.

干预措施: Epilepsy Journey web-based modules (Behavioral)

Epilepsy Journey web-based modules + telehealth with a therapist

Experimental

Participants will receive both the Epilepsy Journey web-based modules and telehealth sessions with a therapist weekly. Participants will review 10 modules independently (~15-30 minutes) and complete 10 telehealth sessions (~30-45 minutes each session) within a 14-week time frame.

干预措施: Epilepsy Journey web-based modules (Behavioral)

Epilepsy Journey web-based modules + telehealth with a therapist

Experimental

Participants will receive both the Epilepsy Journey web-based modules and telehealth sessions with a therapist weekly. Participants will review 10 modules independently (~15-30 minutes) and complete 10 telehealth sessions (~30-45 minutes each session) within a 14-week time frame.

干预措施: Telehealth with a therapist (Behavioral)

Telehealth with a therapist alone

Experimental

Participants will meet with a therapist for 10 telehealth sessions (30-45 minutes each session) within a 14-week time frame.

干预措施: Telehealth with a therapist (Behavioral)

Treatment as Usual

No Intervention

Participants will receive no active behavioral health treatment components and will be followed in usual epilepsy care for 14 weeks.

结局指标

主要结局

Behavior Rating Inventory of Executive Function (2nd edition) Global Executive Composite T-score (parent)

时间窗: 26-weeks post-randomization

The parent-reported BRIEF-2 Global Executive Composite T-score will be used as the primary outcome measure. T-scores are linear transformations of raw scores, where 50 points represent the mean, and 10 points represent the standard deviation. T-scores provide information about an individual's score relative to a normal standardization sample, based on age and sex. T-scores ≥ 65 are considered clinically significant.

次要结局

  • PedsQL™ Epilepsy Module - Impact Subscale (Adolescent report)(26-weeks post-randomization)
  • PedsQL™ Epilepsy Module - Cognitive Functioning Subscale (Adolescent report)(26-weeks post-randomization)
  • PedsQL™ Epilepsy Module - Executive Functioning Subscale (Adolescent report)(26-weeks post-randomization)
  • PedsQL™ Epilepsy Module -Sleep Subscale (Adolescent report)(26-weeks post-randomization)
  • PedsQL™ Epilepsy Module -Mood/Behavior Subscale (Adolescent report)(26-weeks post-randomization)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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