Trial · NCT07904572
Regional Efforts to Advance School-based Sun Safety Through Collaboration for Skin Health
NCT07904572, Not applicable, Enrolling by invitation, University of Utah
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Regional Efforts to Advance School-based Sun Safety Through Collaboration for Skin Health. Trials, record NCT07904572. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07904572
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Regional Efforts to Advance School-based Sun Safety Through Collaboration for Skin Health
- NCT number
- NCT07904572
- Status
- Enrolling by invitation
- Phases
- Not applicable
- Enrollment
- 450 participants, estimated
- Lead sponsor
- University of Utah
- Conditions
- Skin Cancer Prevention, Sun Safety
- Interventions
- REACH West
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Percentage of teachers who completed the intervention without major technical issues | One Month Post Intervention | To measure the intervention feasibility, we will measure the percentage of teachers that completed delivery of the intervention without major technical issues. This is measured by a post-intervention interview that asks, 'Did you encounter any challenges in using the REACH West curriculum in utilizing/accessing the online Canvas modules?' A lower percent of teachers who report encountering issues is a better outcome. |
| Primary | Mean of Intervention Acceptability via AIM | Immediately Post Intervention | We will measure teachers' self-reported acceptability with the intervention via AIM (Acceptability of Intervention Measure). This is measured through four 5-point Likert scale statements (completely disagree to completely agree): * REACH West meets my approval. * REACH West is appealing to me. * I like REACH West. * I welcome REACH West. A higher score indicates a better outcome. |
| Secondary | Mean of Student Tanning Occurrence | Baseline, 1-Month Post-Intervention | We will measure students' self-reported tanning occurrence of the past month. This will include responses to unintentional and intentional tanning questions. Questions include: In the past month, how many times did you.. * Use an indoor tanning device such as a sunlamp, sunbed or tanning booth? (Do not count getting a spray-on tan) * Sunbathe or tan outdoors? * End up with a tan, even if you didn't try to get one? A lower number indicates a better outcome. |
| Secondary | Mean of Student Sun Protection Behaviors | Baseline, 1-month post-intervention | We will measure students' self-reported sun safety behaviors of the past month. This is measured by eight 5-point likert scale items (never to always). Statements include: In the past month, when you were outdoors in the sun for 15 minutes or more, how often did you... * use sunscreen? * re-apply sunscreen after being outside for 2 hours, in the water, or sweating? * wear a shirt with sleeves that cover your shoulders? * wear long pants or a long skirt? * wear a hat? * stay in shade or under an umbrella? * avoid being in the sun between 10:00am-4:00pm? * wear sunglasses? A higher score indicates a better outcome. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07904572
GET https://conductscience.org/api/trials/v1/NCT07904572/registered