MedPath

Randomised Control Trial of the Learn to Be Safe with Emmy and FriendsTM Program: Evaluating Changes in Protective Behaviours Knowledge, Intentions and Disclosure of First Grade Students

Not Applicable
Conditions
Enhancing protective behaviours
Public Health - Health promotion/education
Mental Health - Studies of normal psychology, cognitive function and behaviour
Registration Number
ACTRN12615000917538
Lead Sponsor
Griffith University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Stopped early
Sex
All
Target Recruitment
1620
Inclusion Criteria

All first grade children participating in Learn to BE SAFE with Emmy program or on waitlist for program.

Exclusion Criteria

Previous participation in a protective behaviours program. No parental or child consent.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary Outcome 1: Protective Behaviours knowledge (via Protective Behaviours Questionnaire)[Timepoint: Pre (Baseline), Post (5 weeks after Pre), 6 month follow up, 1 year follow-up and 18 month follow up. ];Primary Outcome 2: Disclosure (via Observed Protective Behaviours Test)[Timepoint: Post (5 weeks after Baseline), 6 month follow up];Primary Outcome 3: Protective Behaviours intentions (via Application of Protective Behaviours Test Revised)[Timepoint: Pre (Baseline), Post (5 weeks after Pre), 6 month follow up, 1 year follow-up and 18 month follow up. ]
Secondary Outcome Measures
NameTimeMethod
Secondary outcome 1: Parentally observed protective Behaviours knowledge and behaviour (via Parent Protective Behaviour Checklist)[Timepoint: Pre (Baseline), Post (5 weeks after Pre), 6 month follow up, 1 year follow-up and 18 month follow up];Secondary Outcome 2: Parental satisfaction (via Parent Satisfaction Questionnaire)[Timepoint: Post (5 weeks after Baseline)];Secondary Outcome 4: Standardised Administration (via session checklists)[Timepoint: Weekly each session between Pre (Baseline) and Post (5 weeks after Pre)];Secondary Outcome 5: Anxiety (via Revised Child Manifest Anxiety Scale-2)[Timepoint: Pre (Baseline), Post (5 weeks after Pre), 6 month follow-up, 1 year follow-up and 18 month follow-up];Secondary Outcome 6: Protective Behaviours (via Observed Protective Behaviours Test)[Timepoint: Post (5 weeks after Baseline), 6 month follow-up]
© Copyright 2025. All Rights Reserved by MedPath