Data

Partners in Parenting: Evaluating the real-world use and impact of an online tailored parenting program for parents of adolescents.

Monash University

Dataset description

An open access trial examining the effects of an individually-tailored, web-based parenting program (Partners in Parenting) for parents of 12-to-17-year-olds to reduce risk and protective factors for adolescent depression and anxiety disorders.
This study is linked to the following two previous trials. These trials were RCTs of the program being evaluated in the current open access trial.
ACTRN12615000328572 was an RCT evaluating the full Partners in Parenting program for parents of adolescents, compared to an active control condition (educational materials).
ACTRN12615000247572 was an RCT of a brief version of the Partners in Parenting program (single session, pesonalised feedback only), compared to a waitlist control.
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Source Study

Purpose

Prevention

Phase

Not Applicable

Funding

Charities/Societies/Foundations,Helen Macpherson Smith Trust

Scientific enquiries

A/Prof Marie Yap

Brief Summary

The study aims to evaluate the real-word effects of the Partners in Parenting program (PiP), an individually-tailored web-based parenting program that aims to teach parents strategies that are believed to reduce their adolescent's risk of developing depression and anxiety disorders, PiP provides parents with personalised feedback about their current parenting, including strengths and areas for improvement, and parents can choose up to 9 interactive online modules designed to support them in maki ....
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Key Inclusion Criteria

Parent or guardian of at least one child aged 12 to 17 years (inclusive) at baseline, who reside in Australia, consider themselves fluent in English, and have internet access and an email account.

Key Exclusion Criteria

No exclusion criteria specified. We will not exclude parents who report clinically elevated symptoms of anxiety or depression in their adolescents at baseline. However, by assessing baseline symptoms, we will be able to conduct subsidiary subgroup analyses of parents of adolescents above/below clinical cut-off scores on the symptom measures, to examine the program effects on these subgroups. The cut-off scores used to determine symptom elevation will be based on published cut-off scores, as foll ....
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Can healthy volunteers participate?

Yes

 

Population

Sample Size    741

Min. age    18 Years

Max. age    No limit

Sex    Both males and females

Condition category    Adolescent anxiety , Adolescent depression , Parent-adolescent attachment , Parental self-efficacy , Risk and protective factors for adolescent depression and anxiety disorders that parents can potentially modify

Condition code    Mental Health

Intervention

Intervention code Behaviour , Lifestyle , Prevention

The intervention is a web-based parenting program called Partners in Parenting (PiP). PiP consists of three components: 1) parents first complete an online self-assessment of their current parenting practices (the Parenting to Reduce Adolescent Depression and Anxiety Scale [PRADAS]). The PRADAS assesses parenting practices in relation to the recommendations in the evidence-base parenting guidelines "How to Prevent Depression and Clinical Anxiety in your Teenager: Strategies for Parents" (Parenti ....
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Comparison

Control group Uncontrolled

No control group

Outcomes

Outcome: Parental risk and protective factors for adolescent depression and anxiety disorders, as measured by the total score on the Parenting to Reduce Adolescent Depression and Anxiety Scale (PRADAS). The PRADAS is a composite measure of several risk and protective factors, hence the total score is the primary outcome of interest.
Timepoint: The PRADAS will be completed at baseline and at 3-months (90 days) post-baseline completion date.

Study Protocol: Not Available
Data Dictionary: Not Available

Will individual participant data (IPD) for this trial be available?

yes

What data in particular will be shared?

De-identified individual participant data underlying published results (i.e. responses to the outcome measures listed).

When will data be available?

Immediately following publication. No end date determined.

Available to whom?

Case-by-case basis at the discretion of the Primary Sponsor.

Available for what types of analyses?

IPD meta-analyses, or any other purpose deemed appropriate by the Primary Sponsor.

Source study information is derived from the Australian New Zealand Clinical Trials Registry (ANZCTR). For more information on the ANZCTR, please see anzctr.org.au