跳至主要内容
临床试验/NCT07075614
NCT07075614Enrolling By Invitation不适用

The Effectiveness of a Parent Training Program for Children With Autism Spectrum Disorder and High-Risk Infants: A Case-Control Study

Umraniye Education and Research Hospital2 个研究点 分布在 2 个国家目标入组 250 人开始时间: 2024年7月10日最近更新:
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
250
试验地点
2
主要终点
Change from Baseline in Autism Severity as Measured by the Childhood Autism Rating Scale (CARS)

研究概览

简要总结

The aim of this study is to evaluate the effectiveness of a parent training program on the severity of autism-related symptoms in two groups: (1) infants under the age of 2 who show early signs of autism, and (2) children aged 2 to 5 years who have been diagnosed with Autism Spectrum Disorder (ASD). The study also aims to assess the program's impact on the quality of life and stress levels of the children's parents or caregivers.

The study will include children aged 0 to 5 years who are either considered at risk for autism or have an ASD diagnosis, along with their caregivers. A total of 250 participants are expected to enroll in the study. Informed consent will be obtained from all parents or caregivers before participation.

After consent, the 250 children will be randomly assigned to one of two groups:

Group A: Parent Training Program + Routine Care Group B: Routine Care Only While Group B will receive standard treatments such as education and psychotherapy and a single psychoeducational session about autism and its treatment, Group A will receive the same routine care plus the structured Parent Training Program.

Children in both groups will be assessed before the intervention begins and again after 12 weeks. Evaluations will be conducted with the support of professionals using standardized tools. Caregivers will complete a background information form with the help of the research team.

To assess symptom severity, the Modified Checklist for Autism in Toddlers (M-CHAT), the Childhood Autism Rating Scale (CARS), and the Clinical Global Impression Scale (CGI) will be administered by clinicians. General developmental levels will be evaluated using screening tools such as the Denver Developmental Screening Test or AGTE. Caregivers will also complete the Quality of Life in Autism-Parent Version and the Parenting Stress Index.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
0 Months 至 5 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Having a child over the age of 2 diagnosed with Autism Spectrum Disorder (ASD), or having a high-risk infant under the age of 2 showing signs of autism
  • Willingness to participate in the study
  • Parent/caregiver must have completed at least primary school education

排除标准

  • Refusal to participate in the study
  • The child has a sensory, physical, or neurological disorder
  • The parent or primary caregiver has a diagnosed psychiatric disorder that significantly impairs functioning
  • The parent or caregiver has any physical illness that affects their interaction with the child (e.g., physical disability, visual or auditorial impairment)

研究组 & 干预措施

Intervention Group

Active Comparator

Parent Training Program + Routine Care

干预措施: Parent Training Program (Behavioral)

Control Group

Other

routine care

干预措施: routine care (Other)

结局指标

主要结局

Change from Baseline in Autism Severity as Measured by the Childhood Autism Rating Scale (CARS)

时间窗: Baseline, After 1 and 3 Months from Intervention

Autism severity will be assessed using the Childhood Autism Rating Scale (CARS), a clinician-rated tool that evaluates behavior in 15 areas related to communication, social interaction, and sensory responses. Each item is rated on a scale from 1 (no signs of autism) to 4 (severe symptoms), with a total score ranging from 15 to 60. The total CARS score will be recorded at baseline (prior to intervention) and again. The primary outcome is the change in total score, which reflects improvement or worsening in the severity of autism symptoms over time.

次要结局

未报告次要终点

研究者

发起方
Umraniye Education and Research Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Prof. Dr. Canan Tanıdır

Prof Dr

Istanbul Gelisim University

研究点 (2)

Loading locations...

相似试验

The Effectiveness of a Parent Training Program for... | 临床试验