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Child Behavior Problem clinical trials

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NCT ID: NCT05444205 Recruiting - Child Development Clinical Trials

The Pittsburgh Study Early Childhood

TPS-ECC
Start date: June 2, 2020
Phase: N/A
Study type: Interventional

The Early Childhood Collaborative of The Pittsburgh Study is a community-partnered, county-wide implementation of programs for children and families from birth through formal school entry to address real-world challenges that exist in providing effective preventive interventions for families with young children, particularly low-income families.

NCT ID: NCT05096611 Recruiting - Clinical trials for Child Behavior Problem

Attachment and Biobehavioral Catch-up and Depression Treatment

ABC+D
Start date: March 1, 2022
Phase: N/A
Study type: Interventional

Maternal depression influences the development of children's behavior problems and vice versa; however most interventions singularly address maternal depression or children's behavior problems rather than both. This project assesses the efficacy of an intervention that treats both mothers and children in an integrated manner. Effects are expected to disrupt the reciprocal relations that perpetuate maternal and child mental health problems over time.

NCT ID: NCT04946253 Recruiting - Clinical trials for Child Behavior Problem

SKIP for PA Study: Team and Leadership Level Implementation Support for Collaborative Care

SKIPforPA
Start date: November 29, 2021
Phase: N/A
Study type: Interventional

In a prior application (MH064372), the investigators' treatment research program (Services for Kids In Primary-care, SKIP) developed and tested a chronic care model-based intervention, called Doctor Office Collaborative Care (DOCC), that was found to be effective in the management of childhood behavior problems and comorbid ADHD. In the "SKIP for PA Study", the investigators propose to conduct a randomized clinical trial to evaluate the effects of team- and practice leadership-level implementation strategies designed to enhance the use and uptake of DOCC in diverse pediatric primary care offices.

NCT ID: NCT04942145 Recruiting - Clinical trials for Child Behavior Problem

Effect of Virtual Reality on Dental Patients

Start date: January 10, 2018
Phase: N/A
Study type: Interventional

Clinicians should appreciate the effectiveness of virtual reality (VR) headsets for managing both the anxiety and the behaviour of dental patients. The aim of this study was to assess the effectiveness of using a VR headset as a distraction for managing the anxiety and behaviour of patients during their dental treatment related to underlying psychological factors.

NCT ID: NCT04821856 Recruiting - Clinical trials for Intellectual Disability

Evaluation of the Effectiveness of Cannabidiol in Treating Severe Behavioural Problems in Children and Adolescents With Intellectual Disability

Start date: May 11, 2021
Phase: Phase 2
Study type: Interventional

This is a multi-site, double-blind, parallel group, randomized, placebo-controlled study of 140 participants comparing oral purified cannabidiol isolate (CBD) with placebo in reducing Severe Behavioral Problems (SBP) at 8 weeks in children aged 6 - 18 years with Intellectual Disability (ID). Eligible participants will be randomized 1:1 to receive either CBD or placebo.

NCT ID: NCT04702191 Recruiting - Parenting Clinical Trials

Promoting Healthy Families: A Canadian Evaluation

Start date: February 10, 2021
Phase: N/A
Study type: Interventional

Interventions that promote safe, stable, and nurturing relationships between caregivers and children are key to improving healthy family relationships, reducing child socioemotional and behaviour problems, and preventing child maltreatment. Although a broad range of parenting programs are currently implemented in communities across Ontario, most programs are inadequately evaluated, or else not evaluated at all. Using a three-armed randomized controlled trial, the aim of the current study is to evaluate the effectiveness of two parenting programs, the Triple P - Positive Parenting Program (group - level 4) and the Circle of Security Parenting Program (group) compared to treatment as usual in Ontario, Canada.

NCT ID: NCT04635969 Recruiting - Clinical trials for Intellectual Disability

Determining the Effectiveness of Sexual Health and Development Education for Children With Intellectual Disability

Start date: February 15, 2021
Phase: N/A
Study type: Interventional

By integrating sexuality and disability literatures, theories, and research, this study aims to: determine the effectiveness of sexual health and development education for children (12-18 years) with mild to moderate intellectual disability. The research hypotheses are as follows: H0: There is no significant difference between the intervention group and the control group in the mean score of the "Sexual Development Characteristics Scale of Children with Mentally Retardation in Adolescence" after the sexual health and development trainings given to children with intellectual disabilities. H1: After the sexual health and development trainings given to children with intellectual disabilities, the mean score of the "Sexual Development Characteristics Scale of Children with Intellectual Disability in Adolescence" is significantly higher in the intervention group compared to the control group.

NCT ID: NCT03910491 Recruiting - Parenting Clinical Trials

Positive Parenting Program in Foster Care

Start date: April 16, 2019
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate early implementation outcomes of a positive parenting program, Child Adult Relationship Enhancement in Primary Care (PriCARE), in the foster care setting and to assess the efficacy of PriCARE in promoting positive parenting and increasing empathy among foster caregivers.

NCT ID: NCT03578016 Recruiting - Clinical trials for Child Behavior Problem

COS-P for Parents of Children Referred to Child Psychiatric Services

COS-P
Start date: August 15, 2018
Phase: N/A
Study type: Interventional

Background:The quality of attachment is greatly influenced by parental sensitivity. Attachment based interventions are designed to promote parental sensitivity, to change parental mental representations and to improve understanding of the developmental needs of the child. Very few studies have investigated the effect of attachment-based interventions on psychiatric symptoms in children. Targeting parental sensitivity and the parent-child interaction might have an important impact on psychiatric symptoms in a clinical sample of children referred to child psychiatric services. Objectives: The primary objective is to investigate whether Circle of Security-Parenting (COS-P) has an effect on parental sensitivity in parents of children referred to child psychiatric services. The secondary objectives are to investigate the effect on children's behavioral and emotional symptoms and the parental stress and reflective functioning after 10 weeks of intervention and at the 24 week follow-up. The study is also exploring the effect of parental attachment style, parental stress and parental psychopathology on the effect of the intervention. Methods: The trial will include 128 families of children (age 3-8 years) who are referred to child psychiatric services in a randomized and controlled design. Included families will be randomized to COS-P+ Treatment as Usual (TAU) or TAU only. Perspectives: Considering the important impact of the quality of the parent-child relationship on the child's well-being, it is essential to target it in interventions and to investigate the relation with psychiatric symptoms. Generally there is a lack of interventions targeting parental sensitivity in psychiatric child populations. Working with the parents on the child-parent relation, might have an important impact on their children's current psychiatric symptoms and could additionally prevent future psychopathology.