Purpose

The goal of this study is to explore possible benefits of Parent-Child Interaction Therapy (PCIT). The main goals of the study are: - To investigate whether pre-survey measures of autonomic reactivity relate to the overall functioning of participants. - To examine the effects of PCIT To identify individual characteristics that influence the effects of PCIT. Participants will: - complete 5 online surveys (1x pre-PCIT, 3x during PCIT, and 1x post-PCIT) - complete the PCIT program

Conditions

Eligibility

Eligible Ages
Between 18 Years and 89 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Parents of children aged 2-7 years old who are eligible for Parent-Child Interaction Therapy (PCIT) based on behavioral concerns. - The primary caregiver of the child and be actively involved in the child's daily care. - Willing to attend all PCIT sessions and complete pre-, mid- and post-intervention assessments. - Fluent in English to ensure comprehension of the intervention and assessment materials.

Exclusion Criteria

  • Parents with diagnosed severe mental health disorders (e.g., schizophrenia, bipolar disorder) that may interfere with participation in PCIT. - Children with conditions that require interventions other than PCIT (e.g., severe developmental disabilities). - Parents who have previously participated in PCIT are excluded to avoid confounding results.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Other

Arm Groups

ArmDescriptionAssigned Intervention
PCIT Group All participants will complete the five online surveys and provide two saliva samples.
  • Behavioral: Parent-Child Interaction Therapy (PCIT)
    Participants will undergo the standard PCIT program, which consists of two phases: Child-Directed Interaction (CDI) and Parent-Directed Interaction (PDI). - CDI Phase: Parents will learn and practice techniques that focus on strengthening the parent-child relationship through play and positive reinforcement. - PDI Phase: Parents will be coached in effective discipline strategies to manage their child's behavioral problems.

Recruiting Locations

More Details

Status
Recruiting
Sponsor
University of Florida

Study Contact

Britney Duner, LCSW
(904) 383-1038
Britney.Duner@jax.ufl.edu

Detailed Description

It is the specific intent of this proposal to experimentally explore the possible benefits and mechanisms through which PCIT can influence self-reported stress and autonomic and neuroendocrine functioning in parents. This will be accomplished by our team by using well-validated self-report measures of mental health, autonomic reactivity, parental stress and attachment, and non-invasive measurements of levels of oxytocin. Specific Aim 1: To investigate whether pre-intervention measures of ANS reactivity and the neuropeptides oxytocin relate to the overall functioning of the participants. - The investigators will examine how measures of autonomic reactivity and levels of oxytocin relate to prior mental/medical health. - Hypothesis: Participants with lower levels of oxytocin and/or increased autonomic reactivity will report being more impacted by their prior adversity and having more emotional/physical symptoms. Specific Aim 2: To investigate the impact of PCIT - The investigators will explore whether PCIT leads to improvements in parental stress, parent-child attachment, and parental neuroendocrine functioning. - Hypothesis: Parents will show a significant decrease in perceived stress and improvement in emotional wellbeing oxytocin levels following CDI. They will also show a decrease in perceived stress, and improvement in attachment and emotional wellbeing following the entire PCIT intervention. Specific Aim 3: To identify individual characteristics that influence the effectiveness of PCIT. - The investigators will explore the impact of specific vulnerability and resiliency factors (e.g., stress, prior adversity) on how well parents benefit from PCIT - Hypothesis: Parental stress and prior mental/medical adversity will negatively impact the effectiveness of intervention

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.