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NCT04341064: SHINE
Sun-safe Habits Intervention and Education
Phase 3 trial testing SHINE Intervention in Skin Cancer in 2,223 participants. Completed in 15 July 2025.
15 July 2025
Quick facts
| Lead sponsor | University of Utah |
|---|---|
| Phase | Phase 3 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 2,223 |
| Start date | 14 September 2020 |
| Primary completion | 15 July 2025 |
| Estimated completion | 15 July 2025 |
| Sites | 1 location across United States |
Drugs / interventions tested
- SHINE Intervention
Conditions studied
- Skin Cancer — all drugs for Skin Cancer →
- Adolescents — all drugs for Adolescents →
Sponsor
University of Utah
Who can join
Adults 11 to 21, any sex, with Skin Cancer or Adolescents. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to determine the efficacy of the Sun-safe Habits Intervention and Education (SHINE) intervention in improving sun protection use and decreasing intentional tanning among high school students. It's anticipated that 30 schools will be randomized into the trial, with approximately half assigned to SHINE and the other half assigned to standard education. After randomization and a baseline assessment, each school will receive two in-class intervention sessions delivered by an interventionist. Follow-up assessments will be completed one month post-intervention, 3-4 months post-intervention, one year post-baseline, and one year post-intervention.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Challenges and lessons learned in recruiting participants for school-based disease prevention programs during COVID-19.
Wu YP, Brunsgaard EK, Siniscalchi N, Stump T, et al · · 2024 · cited 1× · PMID 39698166 · DOI 10.1016/j.conctc.2024.101399 -
Protocol for a cluster-randomized trial of a school-based skin cancer preventive intervention for adolescents.
Wu YP, Stump TK, Hay JL, Buller DB, et al · · 2024 · cited 1× · PMID 38458557 · DOI 10.1016/j.cct.2024.107494
Verify or expand the search:
- PubMed search for NCT04341064
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04341064 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Utah
- Last refreshed: 14 October 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04341064.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing