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OpenTrials
Completed

NCT Number: NCT00593515

Effects of Parental Behavior on Child Anxiety Regulation

Does parenting style affect emotion regulation among children who initially demonstrate high levels of fear and anxiety? Although recent correlational research has demonstrated a linkage between parental behaviors, such as excessive intrusiveness, and children's manifestations of fear and anxiety, it is not clear if parenting behaviors directly influence children's ability to regulate these emotions. Alternatively, these parental behaviors may be elicited by children who express fears and anxieties more frequently than other children do. Experimental research designs would offer a more definitive test of these competing explanations of the extant correlational findings. Intervention studies, in particular, can test whether experimentally manipulating current family interaction patterns affects children's ability to regulate emotion. This study provides a preliminary experimental test of the relationship between parental behavior and children's regulation of fear and anxiety. Some 40 clinically anxious youth, aged 6-13, were randomly assigned to a family intervention program for childhood anxiety problems, which includes extensive parent communication training, or a child intervention program without parent-training. By comparing these two interventions, we tested if it was possible to improve parenting behaviors-such as intrusiveness-through intensive parent-training, above and beyond the effects of involving children in a child intervention program. We then tested the impact of this change in parental behaviors on children's ability to regulate fear and anxiety. We hypothesized that parent-training would reduce intrusiveness, which would in turn improve children's anxiety outcomes.

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Key information

Age range

6 year–13 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

UCLA

Los Angeles, California, 90095, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The child met DSM-IV criteria for a diagnosis of a principal anxiety disorder based on a semi-structured interview
  • The child was not taking any psychiatric medication at the initial assessment, or was taking a stable dose of psychiatric medication (i.e., at least one month at a stable dose prior to the baseline assessment), and
  • If medication was being used, families stated an intention to maintain that dose throughout the study.

Exclusion criteria

  • The child was currently in child-focused psychotherapy
  • The family was currently in family therapy or a parenting class
  • Either the child or the parents evidenced psychotic symptoms
  • The child began taking psychiatric medication or increased his/her dose of medication during the intervention, or
  • For any reason the child or parents appeared unable to participate in the intervention program.

Treatment and study plan

Family cognitive behavioral therapy

Behavioral

12-16 weekly sessions of family cognitive behavioral therapy, 60-80 minutes each

Child-focused cognitive behavioral therapy

Behavioral

12-16 weekly sessions of child-focused cognitive behavioral therapy, 60-80 minutes each

Primary outcomes

  1. Anxiety Disorders Interview Schedule--Child and Parent Versions

    Time frame: Posttreatment

Secondary outcomes

  1. Multidimension Anxiety Scale for Children

    Time frame: Posttreatment

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Important dates

Study start
2000
Primary completion
2004
Study completion
2004
First posted
Jan 15, 2008
Registry last updated
Jan 15, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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