UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000061953 |
|---|---|
| Receipt number | R000070884 |
| Scientific Title | Effect of a Web-Based Educational Intervention Delivered During Healthcare Facility Waiting Time on Medication Adherence: A Non-Randomized Controlled Study |
| Date of disclosure of the study information | 2026/06/22 |
| Last modified on | 2026/06/17 17:45:14 |
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Basic information
Public title
Effect of a Web-Based Educational Intervention Delivered During Hospital Waiting Time on Medication Adherence
Acronym
Hospital Waiting-Time Web Education Study
Scientific Title
Effect of a Web-Based Educational Intervention Delivered During Healthcare Facility Waiting Time on Medication Adherence: A Non-Randomized Controlled Study
Scientific Title:Acronym
Web-Based Education During Healthcare Facility Waiting Time and Medication Adherence Study
Region
| Japan |
Condition
Condition
Diabetes Mellitus
Classification by specialty
| Medicine in general |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
This study aims to develop a web-based educational intervention targeting misconceptions and irrational beliefs about medications among patients with diabetes receiving pharmacological treatment and to evaluate its effect on medication adherence.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Between-group difference in change in medication adherence scores from baseline to post-intervention
Key secondary outcomes
Between-group difference in change inMedication Knowledge Test and Health literacy from baseline to post-intervention
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Non-randomized
Randomization unit
Blinding
Single blind -participants are blinded
Control
No treatment
Stratification
NO
Dynamic allocation
NO
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Behavior,custom |
Interventions/Control_1
Participants will complete a medication-related beliefs questionnaire on an iPad. After each response, tailored educational content, including the correct answer and an explanation addressing common misconceptions and inappropriate beliefs regarding medication use, will be displayed.
Interventions/Control_2
Participants will complete a medication-related beliefs questionnaire on an iPad.
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
| 60 | years-old | > |
Gender
Male and Female
Key inclusion criteria
Outpatients at Kurashiki Central Hospital aged 20 to 59 years who are prescribed oral medication for diabetes mellitus and are scheduled for a follow-up visit within 2 months.
Able to use an iPad without difficulty.
Willing and able to provide informed consent.
Key exclusion criteria
Patients who do not provide informed consent to participate in the study.
Target sample size
150
Research contact person
Name of lead principal investigator
| 1st name | Hirono |
| Middle name | |
| Last name | Ishikawa |
Organization
Teikyo University
Division name
Graduate School of Public Health
Zip code
173-8605
Address
2-11-1 Kaga, Itabashi-ku, Tokyo, 173-8605, Japan
TEL
03-3964-1211
hirono-tky@umin.ac.jp
Public contact
Name of contact person
| 1st name | Kiwa |
| Middle name | |
| Last name | Masunaga |
Organization
Teikyo University
Division name
Graduate School of Public Health
Zip code
173-8605
Address
2-11-1 Kaga, Itabashi-ku, Tokyo, 173-8605, Japan
TEL
03-3964-1211
Homepage URL
25km20018kr@stu.teikyo-u.ac.jp
Sponsor or person
Institute
Teikyo University
Institute
Department
Personal name
Funding Source
Organization
Ministry of Education, Culture, Sports, Science and Technology (MEXT)
Organization
Division
Category of Funding Organization
Japanese Governmental office
Nationality of Funding Organization
Japan
Other related organizations
Co-sponsor
Kurashiki Central Hospital
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Teikyo University Medical Research Ethics Committee
Address
2-11-1 Kaga, Itabashi-ku, Tokyo, 173-8605, Japan
Tel
03-3964-7256
turb-office@teikyo-u.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
倉敷中央病院（岡山県）
Other administrative information
Date of disclosure of the study information
| 2026 | Year | 06 | Month | 22 | 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
| 2026 | Year | 04 | Month | 28 | Day |
Date of IRB
| 2026 | Year | 06 | Month | 10 | Day |
Anticipated trial start date
| 2026 | Year | 06 | Month | 22 | Day |
Last follow-up date
| 2026 | Year | 12 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2026 | Year | 06 | Month | 17 | Day |
Last modified on
| 2026 | Year | 06 | Month | 17 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070884
