UMIN-CTR Clinical Trial

BACK TOP
UMIN-CTR English Home Glossary (Simple) FAQ Search clinical trials

Name:
UMIN ID:

Recruitment status Preinitiation
Unique ID issued by UMIN UMIN000041412
Receipt No. R000046710
Scientific Title Verification of the efficacy of remote health support program by a pharmacist
Date of disclosure of the study information 2020/09/01
Last modified on 2020/08/14

* 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 efficacy of remote health support program by a pharmacist
Acronym Verification of the efficacy of remote health support program by a pharmacist
Scientific Title Verification of the efficacy of remote health support program by a pharmacist
Scientific Title:Acronym Verification of the efficacy of remote health support program by a pharmacist
Region
Japan

Condition
Condition Healthy Adults
Classification by specialty
Adult
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 To verify the efficacy of remote health support program by a pharmacist
Basic objectives2 Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes Behavior change regarding performing self-medication after 2 months
Key secondary outcomes

Base
Study type Interventional

Study design
Basic design Parallel
Randomization Randomized
Randomization unit Individual
Blinding Open -no one is blinded
Control No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms 2
Purpose of intervention Educational,Counseling,Training
Type of intervention
Behavior,custom
Interventions/Control_1 Intervention group; attending a medication/health class and the remote health support program by a pharmacist for 2 months
Interventions/Control_2 Control group; attending a medication/health class
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 Living in or close to Gifu City, being aged 20 years or more, and having the ability to attend the program
Key exclusion criteria Inability to understand the program, such as visual or hearing impairment
Target sample size 60

Research contact person
Name of lead principal investigator
1st name Hitomi
Middle name
Last name Teramachi
Organization Gifu Pharmaceutical University
Division name Laboratory of Clinical Pharmacy
Zip code 501-1196
Address 1-25-4, Daigakunishi, Gifu-shi, Gifu
TEL 0582308100
Email teramachih@gifu-pu.ac.jp

Public contact
Name of contact person
1st name Tomoya
Middle name
Last name Tachi
Organization Gifu Pharmaceutical University
Division name Laboratory of Clinical Pharmacy
Zip code 501-1196
Address 1-25-4, Daigakunishi, Gifu-shi, Gifu
TEL 0582308100
Homepage URL
Email tachi@gifu-pu.ac.jp

Sponsor
Institute Gifu Pharmaceutical University
Institute
Department

Funding Source
Organization Ministry of Education, Culture, Sports, Science and Technology
Organization
Division
Category of Funding Organization Japanese Governmental office
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

IRB Contact (For public release)
Organization Gifu Pharmaceutical University
Address 1-25-4, Daigakunishi, Gifu-shi, Gifu
Tel 0582308100
Email syomuk@gifu-pu.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
2020 Year 09 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
2020 Year 08 Month 06 Day
Date of IRB
2020 Year 08 Month 06 Day
Anticipated trial start date
2020 Year 10 Month 01 Day
Last follow-up date
2025 Year 06 Month 30 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information

Management information
Registered date
2020 Year 08 Month 14 Day
Last modified on
2020 Year 08 Month 14 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046710

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.