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 | 2025/12/17 10:05:36 |
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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 Western countries, AD education is conducted as part of pharmacy education, but in Japan, very few universities teach the AD concept. Therefore, this study used materials on "Chronic Constipation Treatment Drugs" created by the Japan AD Research Group to educate young pharmacists at our hospital and conduct a pilot investigation into the extent to which this education could influence prescription proposals.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Confirmatory
Trial characteristics_2
Pragmatic
Developmental phase
Not applicable
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
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
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
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
Enrolling by invitation
Date of protocol fixation
| 2025 | Year | 03 | Month | 25 | Day |
Date of IRB
| 2025 | Year | 03 | Month | 25 | Day |
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 | 12 | Month | 17 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066221
