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NCT03824093
High and Low Resource Interventions to Promote HPV Vaccines
NA trial testing AFIX Only in Human Papilloma Virus in 225 participants. Completed in 6 May 2020.
6 May 2020
Quick facts
| Lead sponsor | Children's Mercy Hospital Kansas City |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | health services research |
| Enrollment | 225 |
| Start date | 1 July 2018 |
| Primary completion | 6 May 2020 |
| Estimated completion | 6 May 2020 |
| Sites | 1 location across United States |
Drugs / interventions tested
- AFIX Only
- AFIX+ Provider Communication Training
Conditions studied
- Human Papilloma Virus — all drugs for Human Papilloma Virus →
- Tdap - Tetanus, Diphtheria and Acellular Pertussis Vaccination — all drugs for Tdap - Tetanus, Diphtheria and Acellular Pertussis Vaccination →
- Meningitis, Meningococcal — all drugs for Meningitis, Meningococcal →
- Communication — all drugs for Communication →
Sponsor
Children's Mercy Hospital Kansas City
Who can join
18 and older, any sex, with Human Papilloma Virus or Tdap - Tetanus, Diphtheria and Acellular Pertussis Vaccination. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Human Papillomavirus (HPV) is a significant public health issue affecting nearly 14 million people in the United States. HPV can lead to cervical, oropharyngeal, anal, and penile cancers as well as genital warts.The purpose of this study is to test the comparative effectiveness of two interventions, AFIX only vs. AFIX + communication training, to increase Human Papillomavirus (HPV) vaccination rates among adolescent patients in outpatient clinic settings. Providers and staff at four pediatric practices will be randomized to receive an in-person AFIX consultation or an AFIX consultation combined with communication training and commitment poster displays. Provider and parent data will be collected via a tablet computer RedCap survey. Additional practice and provider level HPV vaccination rates will be collected via patient de-identified claims data. The results of this study could contribute to the existing body of literature that suggests provider recommendations and routine vaccination assessments are key to increasing HPV vaccination uptake. This project has the potential to lead to the implementation and dissemination of low resource interventions to increase HPV vaccination rates among children and adolescents.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT03824093
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Children's Mercy Hospital Kansas City trials
Trials by the same sponsor.
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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 NCT03824093 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Children's Mercy Hospital Kansas City
- Last refreshed: 20 January 2021
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/NCT03824093.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing