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Preliminary evaluation of Fear-less Triple P for parents of anxiety-disordered children

A preliminary evaluation of Fear-less Triple P for parents of anxiety-disordered children: Examining children's anxiety symptomatology post-intervention.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000514505
Enrollment
61
Registered
2015-05-22
Start date
2009-05-27
Completion date
2010-02-01
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This project aims to evaluate the efficacy of a 6-session parenting intervention (Fear-less Triple P) in reducing the anxiety symptomatology of anxiety-disordered children aged 7-14 years. Outcomes will be compared with a wait list control group, and will be examined at post-treatment, 3-month, 6-month and 12-month follow-up.

Interventions

Fear-less Triple P is a 6-session, weekly program for parents of anxiety-disordered children. Sessions are of 60-90 minutes duration, and are administered in small groups of 6-8 families. Administering clinicians include clinical psychologists and intern psychologists - students completing their postgraduate studies in clinical psychology. Content covered includes: Psychoeducation about anxiety; emotional resilience; cognitive challenging; exposure; strategies for managing children's anxiety; a

Fear-less Triple P is a 6-session, weekly program for parents of anxiety-disordered children. Sessions are of 60-90 minutes duration, and are administered in small groups of 6-8 families. Administering clinicians include clinical psychologists and intern psychologists - students completing their postgraduate studies in clinical psychology. Content covered includes: Psychoeducation about anxiety; emotional resilience; cognitive challenging; exposure; strategies for managing children's anxiety; and problem solving. Sessions are recorded in order to be able to review for treatment adherence.

Sponsors

Vanessa Cobham
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
7 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

Children aged 7-14 years meeting criteria for at least one anxiety diagnosis on the ADIS-C with a clinical severity rating of 4 or greater. The age of the parents was not considered relevant for inclusion.

Exclusion criteria

Families simultaneously seeking psychological treatment for the children's anxiety elsewhere. Active psychosis in children. Inability to speak English in parents.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026