UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000056144 |
|---|---|
| Receipt number | R000064149 |
| Scientific Title | Investigating the effects of visual information on pain threshold in chronic pain |
| Date of disclosure of the study information | 2024/11/13 |
| Last modified on | 2024/11/13 14:13:01 |
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Basic information
Public title
Investigating the effects of visual information on pain threshold in chronic pain
Acronym
Investigating the effects of visual information on pain threshold in chronic pain
Scientific Title
Investigating the effects of visual information on pain threshold in chronic pain
Scientific Title:Acronym
Investigating the effects of visual information on pain threshold in chronic pain
Region
| Japan |
Condition
Condition
Chronic pain
Classification by specialty
| Orthopedics | Rehabilitation medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
In order to establish a tailored visual stimulation therapy, this study quantifies individual-specific emotional responses using standardized data on visual stimulus and emotional responses from an international database.
Basic objectives2
Others
Basic objectives -Others
This study investigates a relationship between individual-specific emotional responses and immediate changes in pain threshold.
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Pain threshold
Key secondary outcomes
Valence e.t.c.
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
| 18 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Patients who meet all of the following criteria will be included in this study:
1. Chronic pain
2. No gender specified
3. 18 years old and more
Key exclusion criteria
Patients who meet either or both of the following criteria:
1. Difficulty identifying the content of visual information due to neurological disorders
2. Difficulty identifying the content of visual information due to ophthalmic diseases
Target sample size
200
Research contact person
Name of lead principal investigator
| 1st name | Akihito |
| Middle name | |
| Last name | Yoshida |
Organization
Nagoya University
Division name
Division of Prevention and Rehabilitation Science
Zip code
461-8673
Address
1-1-20 Daiko-minami, Higashi-ku, Nagoya city, Aichi Prefecture, Japan
TEL
052-719-1371
yoshida.akihito.v9@f.mail.nagoya-u.ac.jp
Public contact
Name of contact person
| 1st name | Akihito |
| Middle name | |
| Last name | Yoshida |
Organization
Nagoya University
Division name
Division of Prevention and Rehabilitation Science
Zip code
461-8673
Address
1-1-20 Daiko-minami, Higashi-ku, Nagoya city, Aichi prefecture, Japan
TEL
052-719-1371
Homepage URL
yoshida.akihito.v9@f.mail.nagoya-u.ac.jp
Sponsor or person
Institute
Nagoya University
Institute
Department
Personal name
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
Ethics Review Committee of Nagoya University Graduate School of Medicine
Address
65 Tsurumai-cho, Showa-ku, Nagoya city, Aichi prefecture, Japan
Tel
052-741-2111
iga-shinsa@t.mail.nagoya-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
Other administrative information
Date of disclosure of the study information
| 2024 | Year | 11 | Month | 13 | 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
| 2024 | Year | 11 | Month | 13 | Day |
Date of IRB
Anticipated trial start date
| 2025 | Year | 04 | Month | 01 | Day |
Last follow-up date
| 2034 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
NA
Management information
Registered date
| 2024 | Year | 11 | Month | 13 | Day |
Last modified on
| 2024 | Year | 11 | Month | 13 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064149
