UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000057984
Receipt number R000066221
Scientific Title A Study on the Effects of Academic Detailing on Clinical Decision-Making in Young Hospital Pharmacists with Chronic Constipation
Date of disclosure of the study information 2025/06/01
Last modified on 2025/05/27 16:29:04

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Basic information

Public title

A Study on the Effects of Academic Detailing on Clinical Decision-Making in Young Hospital Pharmacists with Chronic Constipation

Acronym

A Study on the Effects of Academic Detailing on Clinical Decision-Making in Young Hospital Pharmacists with Chronic Constipation

Scientific Title

A Study on the Effects of Academic Detailing on Clinical Decision-Making in Young Hospital Pharmacists with Chronic Constipation

Scientific Title:Acronym

A Study on the Effects of Academic Detailing on Clinical Decision-Making in Young Hospital Pharmacists with Chronic Constipation

Region

Japan


Condition

Condition

chronic constipation

Classification by specialty

Gastroenterology Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

In Europe and the United States, AD education is part of pharmacy education, but in Japan, very few universities teach AD concepts. Therefore, we decided to conduct a pilot study to investigate the extent to which education using materials on chronic constipation treatment drugs created by the Japan AD Study Group can influence prescription proposals by young pharmacists at our hospital.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Comparison of bowel movement satisfaction survey results before and after prescription

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients aged 20 years or older who are taking laxatives as medication brought with them upon admission to hospital.

Key exclusion criteria

Pharmacists who have undergone AD training programmes or AD education

Patients whose primary diagnosis is gastroenterology or gastrointestinal surgery

Target sample size

40


Research contact person

Name of lead principal investigator

1st name SADAAKI
Middle name
Last name YOSHINO

Organization

Narita Hospital, International University of Health and Welfare

Division name

pharmacy department

Zip code

286-8520

Address

852 Hatagata, Narita City, Chiba Prefecture

TEL

0476-35-5600

Email

s.yoshino0609@iuhw.ac.jp


Public contact

Name of contact person

1st name SADAAKI
Middle name
Last name YOSHINO

Organization

Narita Hospital, International University of Health and Welfare

Division name

pharmacy department

Zip code

286-8520

Address

852 Hatagata, Narita City, Chiba Prefecture

TEL

0476355600

Homepage URL


Email

s.yoshino0609@iuhw.ac.jp


Sponsor or person

Institute

Narita Hospital, International University of Health and Welfare

Institute

Department

Personal name



Funding Source

Organization

None

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

International University of Health and Welfare Chiba Region Ethics Review Committee

Address

852 Hatagata, Narita City, Chiba Prefecture

Tel

0476-20-7708

Email

rinri_md@iuhw.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

2025 Year 06 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

Preinitiation

Date of protocol fixation

2025 Year 03 Month 25 Day

Date of IRB


Anticipated trial start date

2025 Year 06 Month 01 Day

Last follow-up date

2027 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

positive observation


Management information

Registered date

2025 Year 05 Month 27 Day

Last modified on

2025 Year 05 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066221