跳至主要内容
临床试验/NCT06125093
NCT06125093已完成不适用

Early Treatment for Children With Mental Health Problems and Genetic Abnormalities Through a Parenting Intervention (The GAP): A Pragmatic Randomized Controlled Trial

Fundació Sant Joan de Déu4 个研究点 分布在 1 个国家目标入组 53 人开始时间: 2023年3月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
53
试验地点
4
主要终点
Parents' acceptability and satisfaction with the program (evaluated with the Autism Program Parent Final Satisfaction Questionnaire)

研究概览

简要总结

The GAP study is a randomized controlled trial that aims to determine the feasibility and efficacy of the "Incredible Years Autism Spectrum and Language Delays" (IY-ASLD®) intervention for families of children with developmental problems from a genetic basis. It is a multicentric trial where families will randomly be assigned to the intervention group or to a control group (they will follow their usual treatment). The intervention will be carried out in an online format, and it will involve 22 weekly group sessions. The results of The GAP study will help clinicians and policy makers in guiding towards evidence-based treatment options for these particularly vulnerable group of infants.

详细描述

Children born with genetic abnormalities have higher risk of presenting developmental and mental health problems. Their parents tend to express higher anxiety levels, as parenting children with developmental problems can be a stressful challenge for many families. These infants can present important behaviour, emotion regulation and social interaction problems. These problems usually have a complex clinical presentation determined by their genetic abnormality. Despite many of their impairing symptoms can overlap with the characteristics of the Autism Spectrum Disorder (ASD), in many cases they do not meet criteria for a full-blown ASD diagnosis. These patients are placed in a double disadvantaged situation, as on top of suffering a genetic disease, they do not usually enter the ASD care-pathways and do not have access to effective therapies for their impairing symptoms. This problem should be addressed, as there is wide scientific evidence on early parenting programs that improve infants' developmental problems and parents' mental health. These parenting programs are structured interventions that provide parenting skills to improve the acquisition of children's social and emotion regulation abilities. Such interventions have been widely implemented internationally, but unfortunately, most families treated within our mental health system still do not have access to them. A good example is the parenting program "Incredible Years Autism Spectrum and Language Delays (IY-ASLD®)", focused on improving young children's development and parental stress levels. Recently, the feasibility and acceptability of implementing this program in different areas of the national territory has been studied, with high satisfaction levels expressed by participant families (parents of children with language delays or ASD). However, the scientific evidence is very limited for children with developmental problems from a genetic basis, particularly for those with dysfunctional symptoms' that do not meet diagnostic threshold for an ASD diagnosis.

The GAP study aims to determine, for the first time, the feasibility and efficacy of the IY-ASLD® intervention for families of children with developmental problems from a genetic basis. It is a multicentric randomized controlled trial where families will randomly be assigned to the intervention group or to a control group (they will follow their usual treatment). As genetic abnormalities are rare, clinicians will carry out the intervention in an online format (22 weekly sessions), reaching out all affected families that live scattered throughout the national territory. The results of The GAP study will help clinicians and policy makers in guiding towards evidence-based treatment options for these particularly vulnerable group of infants.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
3 Years 至 7 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children aged 3.0 - 7.11 years at recruitment
  • Children with a diagnosis or in diagnostic process for high suspicion of a genetic abnormality
  • For children up to 5.11 years with withdrawn (defined as CBCL/1.5-5 scores above the borderline clinical range, T-score> 65) AND/OR pervasive developmental problems (defined as CBCL/1.5-5 scores above the borderline clinical range, T-score> 65) AND/OR socialization difficulties (defined as Vineland-III scores below 1SD in the socialization subdomains).
  • For children over 6 years with social problems (defined as CBCL/6-18 scores above the borderline clinical range, T-score> 65) AND/OR thought problems (defined as CBCL/6-18 scores above the borderline clinical range, T-score> 65) AND/OR socialization difficulties (defined as Vineland-III scores below 1SD in the socialization subdomains).
  • Parents/caregivers showing good understanding of the Spanish or Catalan language
  • Parents/caregivers consenting to take part in the study and signing the informed consent

排除标准

  • Children diagnosed with an Autism Spectrum Disorder
  • Children scoring above diagnostic cut-off for Autism or Autism Spectrum Disorder in the ADOS-
  • Attending another structured parenting program
  • Children in the care of their local authority

结局指标

主要结局

Parents' acceptability and satisfaction with the program (evaluated with the Autism Program Parent Final Satisfaction Questionnaire)

时间窗: Administered to the intervention group at treatment completion (approximately 22 weeks after baseline)

Parents' acceptability and satisfaction with the program will be assessed with the Autism Program Parent Final Satisfaction Questionnaire (included within the IY-ASLD® program). Data will be collected after the last session of the intervention.

Percentage of parents engaging with and finishing the program

时间窗: Attendance sheet completed weekly throughout treatment (22 weeks total)

Parents' attendance at the sessions will be regeristered weekly with a sheet of attendance, with the aim to determine levels of compliance and engagement with the intervention. An attendance of at least 15/22 sessions is expected, with a minimum of 50% of parents finishing the program.

Compliance and satisfaction throughout the study (Autism Program Parent Weekly Evaluation)

时间窗: Questionnaire administered to the intervention group weekly throughout treatment (22 weeks total)

Parents' compliance and satisfaction with the intervention will be assessed weekly after each session with the questionnaire "Autism Program Parent Weekly Evaluation", which is part of the IY-ASLD® program materials.

Parents' overall experiences with the program (evaluated with individual interviews)

时间窗: Interviews to the participants of the intervention group at treatment completion (approximately 22 weeks after baseline)

Individual interviews will be conducted after the last session of the intervention to explore from a qualitative perspective: (1) parents' acceptability, satisfaction and overall experience with the intervention, and (2) parents' perceived changes in their parenting skills and parental distress after the intervention. Outcome measurements 3 and 4 will be combined to determine parents' experiences, acceptability and satisfaction with the program.

次要结局

  • Changes from baseline to post-intervention in Alabama Parenting Questionnaire-Preschool revision (APQ-Pr)(Administered to the intervention and control group at baseline (prior to programme initiation) and at immediately after the intervention (approximately 22 weeks after baseline))
  • Clinicians' experiences with the intervention delivered(Interviews to clinicians at treatment completion (approximately 22 weeks after baseline))
  • Changes from baseline to post-intervention in Autism-Specific Five Minute Speech Sample (ASFMFSS)(Administered to the intervention and control group at baseline (prior to programme initiation) and at immediately after the intervention (approximately 22 weeks after baseline))
  • Changes from baseline to post-intervention in Parent Stress Inventory-Short Form (PSI-SF)(Administered to the intervention and control group at baseline (prior to programme initiation) and at immediately after the intervention (approximately 22 weeks after baseline))
  • Changes from baseline to post-intervention in Beck Depression Inventory (BDI)(Administered to the intervention and control group at baseline (prior to programme initiation) and at immediately after the intervention (approximately 22 weeks after baseline))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

Loading locations...

相似试验