UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000050192
Receipt number R000056969
Scientific Title Verification of educational intervention effects on cervical cancer and HPV vaccines for pharmacists
Date of disclosure of the study information 2023/02/01
Last modified on 2023/05/17 09:51:26

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Verification of the effect of educational intervention on cancer for pharmacists

Acronym

Verification of the effect of educational intervention on cancer for pharmacists

Scientific Title

Verification of educational intervention effects on cervical cancer and HPV vaccines for pharmacists

Scientific Title:Acronym

Verification of educational intervention effects on cervical cancer and HPV vaccines for pharmacists

Region

Japan


Condition

Condition

For healthy adults

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To determine whether educational intervention on cervical cancer and HPV vaccine against pharmacists increases their willingness to recommend the HPV vaccine.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Percentage of pharmacists who suggest HPV vaccination 28 days following an educational intervention

Key secondary outcomes

(1) Percentage of pharmacists who suggest HPV vaccination immediately after educational intervention
(2) Before and after an educational intervention, understanding regarding the HPV vaccine changed
(3) Percentage of pharmacists who posted/distributed posters/pamphlets about HPV vaccines in pharmacies after the educational intervention


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification

NO

Dynamic allocation

NO

Institution consideration


Blocking

YES

Concealment

No need to know


Intervention

No. of arms

2

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Other

Interventions/Control_1

Intervention group: Watched a video about cervical cancer and the HPV vaccine (approximately 20 minutes)

Interventions/Control_2

Control group: Watched a video about lung cancer (approximately 20 minutes)

Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

24 years-old <=

Age-upper limit

75 years-old >=

Gender

Male and Female

Key inclusion criteria

Those who received sufficient explanation regarding the purpose and contents of this research, those who could consent, and those who fully understood the goal of this research and voluntarily agreed to participate.

Key exclusion criteria

(1)Those who declined to participate in the research on their own will
(2)Individuals who are deemed ineligible by the research director

Target sample size

120


Research contact person

Name of lead principal investigator

1st name Nobuyuki
Middle name
Last name Wakui

Organization

Hoshi University

Division name

Division of Applied Pharmaceutical Education and Research

Zip code

142-8501

Address

2-4-41 Ebara, Shinagawa-ku, Tokyo

TEL

03-5498-5760

Email

n-wakui@hoshi.ac.jp


Public contact

Name of contact person

1st name Nobuyuki
Middle name
Last name Wakui

Organization

Hoshi University

Division name

Division of Applied Pharmaceutical Education and Research

Zip code

142-8501

Address

2-4-41 Ebara, Shinagawa-ku, Tokyo

TEL

03-5498-5760

Homepage URL


Email

n-wakui@hoshi.ac.jp


Sponsor or person

Institute

Hoshi University

Institute

Department

Personal name



Funding Source

Organization

Hoshi University

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Hoshi University Research Ethics Committee

Address

142-8501, 2-4-41 Ebara, Shinagawa-ku, Tokyo

Tel

03-3786-1011

Email

somu@hoshi.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2023 Year 02 Month 01 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2023 Year 01 Month 06 Day

Date of IRB

2023 Year 01 Month 06 Day

Anticipated trial start date

2023 Year 02 Month 27 Day

Last follow-up date

2023 Year 05 Month 17 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2023 Year 01 Month 31 Day

Last modified on

2023 Year 05 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000056969


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name