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Clinical Trials/ACTRN12615000328572
ACTRN12615000328572
Completed
未知

Examining the effects of an individually-tailored web-based parenting program (Parenting Strategies) for parents of 12- to 15-year-olds, compared to a control group that receives standard educational materials about adolescent development and mental health, on parental risk and protective factors associated with adolescent depression and anxiety, as well as on adolescent depressive and anxiety symptoms.

Dr Marie Yap0 sites676 target enrollmentApril 9, 2015

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Dr Marie Yap
Enrollment
676
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 9, 2015
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Dr Marie Yap

Eligibility Criteria

Inclusion Criteria

  • Parent Participants:
  • Parents or guardians of at least one child aged 12 to 15 years (inclusive), who reside in Australia, are fluent in English, have regular access to the internet and an email account.
  • Adolescent Participants:
  • Adolescent children of participating parents/guardians, aged 12 to 15 years (inclusive) on entry to the trial, who reside in Australia, are fluent in English, and have regular access to the internet.
  • Only one parent and one adolescent per family can participate in the trial.

Exclusion Criteria

  • 1\. Parents who reside outside of Australia.
  • 2\. Parents who are not proficient in English.
  • Adolescents:
  • 1\. Adolescents who reside outside of Australia.
  • 2\. Adolescents who are not proficient in English.
  • 3\. Adolescents who do not have parental consent to participate in the study; or who do not provide verbal assent to participate. Note: parents can still participate if their child does not participate.
  • Parents and adolescents will not be excluded if the adolescent scores in the clinically elevated range (as determined by published clinical cut\-off scores) on either the SMFQ or SCAS (either parent\- or child\-report form) at baseline. However, by assessing baseline symptoms, we will be able to conduct post\-hoc analyses in which we exclude adolescents who scored above the clinical cut\-off scores at baseline.
  • The cut\-off scores used are as follows:
  • SMFQ (parent\- or child\-report versions): 8 or more
  • SCAS (Child\-report):

Outcomes

Primary Outcomes

Not specified

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