Trials / Completed
CompletedNCT03077646
Pediatric Inpatient Firearm Safety Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 225 (actual)
- Sponsor
- Montefiore Medical Center · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
There is currently no available data regarding using the inpatient setting as an opportunity to talk to parents/guardians about firearm safety. The investigators will be doing a pre-/post-intervention study to investigate the effect of an intervention (a 5.5 minute Be SMART video and written materials developed by the organization Everytown for Gun Safety), on parental/legal guardian knowledge, attitudes and practices regarding firearm safety. While the American Academy of Pediatrics recommends the safest home for children is one without guns, the reality is that there are families with guns in the home. This non-political video focuses on ways to keep children safe from firearms. The investigators will also investigate any additional effect of physician-delivered counseling on parental/guardian knowledge, attitudes and practices regarding gun safety as compared to receiving the information solely via video and written materials. Participants will be randomized to 1 of 3 groups (intervention, intervention + MD discussion and control group). Outcomes will be assessed immediately post intervention and in a 30-day follow up phone call.
Detailed description
Eligibility: All parents/guardians of inpatients admitted to the Children's Hospital at Montefiore. Exclusion: Parents/guardians whose children are in acute distress or in the Pediatric Intensive Care Unit. Outcomes: The primary outcome is the change in parent/legal guardian's behavior over the past 30 days with respect to how often they asked whether or not there are guns in the home when their child/children goes to play in another's person's home, as indicated by a Likert scale assignment of an ordinal value (1-5, 1= never, 2=rarely, 3=sometimes, 4=most of the time, 5=always). Secondary outcomes will include: * Change in the primary outcome (intention to ask noted above) between the intervention groups (Be SMARTalone vs. Be SMART + MD) * Demographic factors associated with primary outcome * Description of general knowledge on firearm safety of parents/legal guardians of patients in our community * Description of attitudes about firearm safety of parents/legal guardians of patients in our community * Description of general practices regarding firearm safety of parents/legal guardians of patients in our community * Description of parents attitudes regarding physicians discussing firearm safety with them
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Be SMART | An educational campaign that is non-political reviewing gun safety measures for preventing firearm injuries in children. There is both a video and written materials reviewing the information. The acronym SMART stands for: Secure all guns in your home, Model responsible behavior, Ask about unsecured guns in other homes, Recognize the risks of teen suicide, Tell your peers to be SMART |
| BEHAVIORAL | Control: TSE | A video called "Kids and Smoke Don't Mix" and handouts on tobacco smoke exposure (TSE) developed by the New York state quit-line. |
| BEHAVIORAL | Be SMART + MD review | An educational campaign that is non-political reviewing gun safety measures for preventing firearm injuries in children. There is both a video and written materials reviewing the information. The acronym SMART stands for: Secure all guns in your home, Model responsible behavior, Ask about unsecured guns in other homes, Recognize the risks of teen suicide, Tell your peers to be SMART. After being presented to parents/guardians via video and handouts, this information will be reviewed in person with a Physician. |
Timeline
- Start date
- 2017-03-01
- Primary completion
- 2019-08-09
- Completion
- 2019-08-09
- First posted
- 2017-03-13
- Last updated
- 2021-02-23
- Results posted
- 2021-02-23
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT03077646. Inclusion in this directory is not an endorsement.