UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000013775
Receipt number R000015925
Scientific Title Refine of program to promote self-monitoring of respiratory infection symptoms
Date of disclosure of the study information 2014/04/21
Last modified on 2014/04/21 17:35:19

* 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

Refine of program to promote self-monitoring of respiratory infection symptoms

Acronym

Refine of program to promote self-monitoring of respiratory infection symptoms

Scientific Title

Refine of program to promote self-monitoring of respiratory infection symptoms

Scientific Title:Acronym

Refine of program to promote self-monitoring of respiratory infection symptoms

Region

Japan


Condition

Condition

chronic obstructive pulmonary disease

Classification by specialty

Nursing

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We develop a revision program to promote self-monitoring of respiratory infection symptoms

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

frequencies of hospital readmissions on acute exacerbations related respiratory infection

Key secondary outcomes



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

Prevention

Type of intervention

Behavior,custom

Interventions/Control_1

Thepatients are ptovided knowledge of respiratory infection,monitoring skills and action plan.Thepatients are requested to implement monitoring at home for six months.The diatirs kept by the subjects are reviewed after discharge.

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

patients who are hospitalized by acute exacerbation

Key exclusion criteria

Subjects are able measure and record their symptoms and have no mentar hearth problems.

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name kosaki ayako

Organization

juntendo university hospital

Division name

Nursing

Zip code


Address

3-1-3Hongo Bunkyo-ku Tokyo

TEL

03-3813-3111

Email

akosaki@juntendo.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Mori Kikuko

Organization

university of hyogo

Division name

Nursing

Zip code


Address

13-71 Kitaouji-tyou Akashi-city

TEL

078-925-9447

Homepage URL


Email

kikuko_mori@cnas.u-hyogo.ac.jp


Sponsor or person

Institute

University of Hyogo

Institute

Department

Personal name



Funding Source

Organization

japans Society for the promotion of Science

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

順天堂大学医学部附属順天堂医院(東京)


Other administrative information

Date of disclosure of the study information

2014 Year 04 Month 21 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

2014 Year 04 Month 04 Day

Date of IRB


Anticipated trial start date

2014 Year 04 Month 04 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2014 Year 04 Month 21 Day

Last modified on

2014 Year 04 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015925