Evaluate Web-based Child Safety Intervention Website for ParentsNCT07804355
Evaluation of an Online Educational Child Injury Prevention Intervention
A study testing Safe Kids Washington in people with Evaluate Web-based Child Safety Intervention Website for Parents, run by University of Oregon at 1 site in United States.
Trial summary
The goal of this evaluation is to learn what effect the Safe Kids Washington website, a self-guided web-based intervention program, has on: Parent knowledge of injury prevention strategies Parent attitudes, self-efficacy and behavioral intention regarding use of the strategies Parent satisfaction with the Safe Kids… Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Evaluate Web-based Child Safety Intervention Website for Parents
- What is being tested?
- Safe Kids Washington
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 203 participants
- Where
- 1 siteUnited States
- Study dates
- 14 May 2025to 15 Feb 2026
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- at least 18 years old
- parent or caregiver of a child between 7 and 12 years old
Who cannot join
- under 18 years old
- not the parent or caregiver of a child between 7 and 12 years old
Trial locations and contacts
1 site in 1 country.
About this study
The goal of this evaluation is to learn what effect the Safe Kids Washington website, a self-guided web-based intervention program, has on:
Parent knowledge of injury prevention strategies Parent attitudes, self-efficacy and behavioral intention regarding use of the strategies Parent satisfaction with the Safe Kids training, and Parent opinion of the Safe Kids website usability, functionality, and perceived usefulness
Read more
The program will be evaluated using a random control design. Participants are randomly assigned to either the Safe Kids Washington condition or to a control condition.
Intervention participants will:
Access three modules, focused on pedestrian safety, bicycling safety, and sports safety with an emphasis on concussion prevention watch a brief informational video with relevant statistics about the injury threat be presented with streamlined injury prevention information like how to wear a helmet correctly watch a brief animated vignette with a fictional story about injury prevention engage in interactive game-like knowledge checks like quizzes and flashcards be provided resources like factsheets, tips and guides for parents
Control participants will:
be provided access to three CDC HEADS UP fact sheets, focused on similar topics of playground safety, bike helmet safety, and concussion tips
- Being tested
- Safe Kids Washington, Active Control condition
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Safe Kids WashingtonOther
Also called Kid Safety Study
three modules, focused on pedestrian safety, bicycling safety, and sports safety that include short informational videos, streamlined injury prevention information, animated vignettes, and interactive knowledge checks
Active Control conditionOther
access to three CDC HEADS UP fact sheets, focused on topics of playground safety, bike helmet safety, and concussion tips
| Study group | Role | What they receive |
|---|---|---|
| Intervention condition | Active comparator | Not described Receives: Other: Safe Kids Washington |
| Active Control condition | Other | A control condition in which participants are provided text-based informational material comparable to the intervention condition content but without the additional engaging module components Receives: Other: Active Control condition |
What is being measured
The primary outcome is the main question the study is designed to answer.
perceived vulnerability
Measured: From pre-test to post-test (typically less than a half hour between)
self-efficacy
Measured: from pre-test to post-test (typically less than a half-hour between)
knowledge
Measured: from pre-test to post-test (typically less than a half-hour between)
behavioral intentions
Measured: From pre-test to post-test (typically less than a half hour between)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Sep 2026
- Study start14 May 2025
- Primary completion15 Feb 2026
- Study completion15 Feb 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Evaluate Web-based Child Safety Intervention Website for ParentsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 203 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Oregon
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Melissa McCart, Ed.D., Principal investigator, University of Oregon
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07804355
- Sponsor's protocol ID
- STUDY00001746
- Status last verified
- Aug 2026
- First submitted
- 31 Aug 2026
- Last updated
- 11 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: All collected IPD are available from the corresponding author, \[M. McCart\], upon reasonable request.
Study at a glance
From the registry record, last updated by the sponsor on 11 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of an Online Educational Child Injury Prevention Intervention
- ClinicalTrials.gov ID
- NCT07804355
- Acronym / sponsor ID
- STUDY00001746
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 203 participants (actual)
- Lead sponsor
- University of OregonUniversity, hospital or other
- Study start
- 14 May 2025 (actual)
- Primary completion
- 15 Feb 2026 (actual)
- Study completion
- 15 Feb 2026 (actual)
- First posted
- 4 Sep 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this evaluation is to learn what effect the Safe Kids Washington website, a self-guided web-based intervention program, has on:
Parent knowledge of injury prevention strategies Parent attitudes, self-efficacy and behavioral intention regarding use of the strategies Parent satisfaction with the Safe Kids training, and Parent opinion of the Safe Kids website usability, functionality, and perceived usefulness
The program will be evaluated using a random control design. Participants are randomly assigned to either the Safe Kids Washington condition or to a control condition.
Intervention participants will:
Access three modules, focused on pedestrian safety, bicycling safety, and sports safety with an emphasis on concussion prevention watch a brief informational video with relevant statistics about the injury threat be presented with streamlined injury prevention information like how to wear a helmet correctly watch a brief animated vignette with a fictional story about injury prevention engage in interactive game-like knowledge checks like quizzes and flashcards be provided resources like factsheets, tips and guides for parents
Control participants will:
be provided access to three CDC HEADS UP fact sheets, focused on similar topics of playground safety, bike helmet safety, and concussion tips
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention condition | Active comparator | Other: Safe Kids Washington |
| Active Control condition | Other | Other: Active Control conditionA control condition in which participants are provided text-based informational material comparable to the intervention condition content but without the additional engaging module components |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- at least 18 years old
- parent or caregiver of a child between 7 and 12 years old
Key exclusion criteria (2 listed)
- under 18 years old
- not the parent or caregiver of a child between 7 and 12 years old
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Safe Kids WashingtonAlso: Kid Safety Studythree modules, focused on pedestrian safety, bicycling safety, and sports safety that include short informational videos, streamlined injury prevention information, animated vignettes, and interactive knowledge checks | Other | Intervention condition |
| Active Control conditionaccess to three CDC HEADS UP fact sheets, focused on topics of playground safety, bike helmet safety, and concussion tips | Other | Active Control condition |
Primary outcome
perceived vulnerability
Time frame: From pre-test to post-test (typically less than a half hour between)
self-efficacy
Time frame: from pre-test to post-test (typically less than a half-hour between)
knowledge
Time frame: from pre-test to post-test (typically less than a half-hour between)
behavioral intentions
Time frame: From pre-test to post-test (typically less than a half hour between)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Sep 2026.
- Individual participant dataSharing planned: Yes. All collected IPD are available from the corresponding author, [M. McCart], upon reasonable request.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Melissa McCart, Ed.D. principal investigator
University of Oregon
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Safe Kids Washington in people with Evaluate Web-based Child Safety Intervention Website for Parents, run by University of Oregon at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 11 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
perceived vulnerability (time frame: From pre-test to post-test (typically less than a half hour between)). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Sep 2026.