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NCT04667702 · ClinicalTrials.gov registry record

HPV Vaccine Hesitancy Among Indiana Youth With Cancer and Blood Diseases

A clinical trial of Human Papilloma Virus Vaccine Hesitancy, sponsored by Indiana University.

Completed
Registry status
176
Enrollment target
1
Study location

NCT04667702: Completed study of Human Papilloma Virus Vaccine Hesitancy, sponsored by Indiana University.

NCT04667702 is a study of Human Papilloma Virus Vaccine Hesitancy that has completed, run by Indiana University. The registered enrollment target is 176 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04667702, a study of Human Papilloma Virus Vaccine Hesitancy, has completed, sponsored by Indiana University.

COMPLETED
Registry status
176 participants
Enrollment target
1
Study location

Study Summary

For the identified groups of patients (survivors of childhood cancer and youth with sickle cell disease) the investigators want to better understand the barriers to, and facilitators of, HPV vaccination. Through HCP interviews the investigators will also assess both attitudinal and logistical obstacles to HPV vaccination. Some subspecialty HCPs may believe, for instance, that it is the primary care provider's responsibility to vaccinate or they may be unfamiliar with the requirement to enter vaccination data into CHIRP. Also, in some cases HPV vaccine may not be readily available in subspecialty clinic locations and/or subspecialty HCPs may not be Vaccines for Children (VFC) providers. Participants: the investigators will focus on two patient groups: survivors of childhood cancer, which includes children aged 9-21 years who have completed active therapy for cancer and are eligible for vaccination, and sickle cell disease, which includes children aged 9-21 years with a diagnosis of sickle cell disease. The investigators will recruit parents of children aged 9-21 years and older adolescents aged 18-21 years. For pediatric patients, the investigators selected a lower age of 9 years because HPV vaccine is licensed down to 9 years of age, and an upper limit of 21 years, as that is considered the upper bound of adolescence by the American Academy of Pediatrics. For patients 9-17 years of age, only parents will be interviewed by video or phone because parents are the vaccine decision-makers. For patients 18-21 years of age, the investigators will interview both young adults and their parents, because, while the young adult has legal decision-making capacity, in reality, the decision is frequently made jointly by the young adult and parent, and older adolescents are frequently unwilling to go against their parents' wishes. All research procedures will be conducted in English. Participants will be excluded if they have an intellectual disability or severe medical illness suc

Primary Outcome

Patients will be scored using scale: 1=strongly disagree; 2=disagree; 3=neither agree nor disagree; 4=agree; and 5=strongly agree; lower scores mean less confidence/more hesitancy; higher scores mean more confidence/less hesitancy.

Interventions

  • BEHAVIORAL Interviews

Study Locations (1)

Indiana

  • Riley Hospital for Children - Indiana University - Indianapolis

Trial Details

FieldValue
Enrollment Target 176 participants
Start Date 2021-01-04
Est. Completion 2022-07-05
Indiana University

890 total trials

What the finished NCT04667702 record still lists

NCT04667702 is an observational study that tracks outcomes without assigning an intervention. The registered 176 participants enrollment target is mid-sized for trials with a published cap.

The record links to 1 condition, with Human Papilloma Virus Vaccine Hesitancy appearing as the primary indexed condition, and to 1 intervention - of which Interviews is the first listed.

NCT04667702 reports a single indexed study location in Indiana.

Frequently Asked Questions

What is clinical trial NCT04667702 about?

NCT04667702 is a clinical study titled "HPV Vaccine Hesitancy Among Indiana Youth With Cancer and Blood Diseases". For the identified groups of patients (survivors of childhood cancer and youth with sickle cell disease) the investigators want to better understand the barriers to, and facilitators of, HPV vaccination. Through HCP interviews the investigators will also assess both attitudinal and logistical obstac...

What is the current status of trial NCT04667702?

This trial is currently completed. The enrollment target is 176 participants. The study started on 2021-01-04. Estimated completion is 2022-07-05.

What conditions does trial NCT04667702 study?

This clinical trial studies the following conditions: Human Papilloma Virus Vaccine Hesitancy.

What interventions are being tested in trial NCT04667702?

The interventions under investigation include: Interviews (BEHAVIORAL).

Who is sponsoring clinical trial NCT04667702?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04667702 being conducted?

This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT04667702, the US trial registry maintained by the National Library of Medicine. NCT04667702 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.