UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000051339
Receipt number R000058566
Scientific Title Study of the usefulness of the STarT back screening tool to predict the effect of acupuncture treatment
Date of disclosure of the study information 2023/06/14
Last modified on 2023/06/14 10:55:49

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Basic information

Public title

Study of the usefulness of the STarT back screening tool to predict the effect of acupuncture treatment

Acronym

Study of the usefulness of the STarT back screening tool to predict the effect of acupuncture treatment

Scientific Title

Study of the usefulness of the STarT back screening tool to predict the effect of acupuncture treatment

Scientific Title:Acronym

Study of the usefulness of the STarT back screening tool to predict the effect of acupuncture treatment

Region

Japan


Condition

Condition

low back pain

Classification by specialty

Orthopedics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the usefulness of STarT back screening tool in acupuncture treatment for patients with low back pain

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Degree of visual analogue scale for low back pain

Key secondary outcomes

STarT back screening tool


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Acupuncture for 4 weeks.

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 with pain in the lower back experienced in the last 4 weeks that lasted for more than 1 day

Key exclusion criteria

Those who already have entered another clinical trials

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Hiroshi
Middle name
Last name Kondo

Organization

Tsukuba University of Technology

Division name

Faculty of Health Science

Zip code

305-8521

Address

4-12-7,Kasuga, Tsukuba, Ibaraki, Japan

TEL

029-852-2890

Email

kondo0207@k.tsukuba-tech.ac.jp


Public contact

Name of contact person

1st name Erika
Middle name
Last name Matsuda

Organization

University of Tsukuba

Division name

Graduate School of Comprehensive Human Sciences

Zip code

305-8572

Address

1-1-1 Tennodai, Tsukuba, Ibaraki, Japan

TEL

029-853-2111

Homepage URL


Email

s2130327@u.tsuuba.ac.jp


Sponsor or person

Institute

sukuba University of Technology, Faculty of Health Science

Institute

Department

Personal name



Funding Source

Organization

Tsukuba University of Technology, Faculty of Health Science

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

Tsukuba University of Technology, Faculty of Health Science

Address

4-12-7,Kasuga, Tsukuba, Ibaraki, Japan

Tel

029-852-2890

Email

sayuzawa@k.tsukuba-tech.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

2023 Year 06 Month 14 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

71

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

Completed

Date of protocol fixation

2022 Year 04 Month 01 Day

Date of IRB

2022 Year 09 Month 13 Day

Anticipated trial start date

2022 Year 09 Month 20 Day

Last follow-up date

2022 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

2023 Year 06 Month 14 Day

Last modified on

2023 Year 06 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000058566


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name