UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000023472
Receipt number R000027039
Scientific Title Effect of recumbent isometric yoga on patients with severe CFS
Date of disclosure of the study information 2016/08/04
Last modified on 2018/02/28 14:48:32

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Basic information

Public title

Effect of recumbent isometric yoga on patients with severe CFS

Acronym

Recumbent isometric yoga for sever CFS

Scientific Title

Effect of recumbent isometric yoga on patients with severe CFS

Scientific Title:Acronym

Recumbent isometric yoga for sever CFS

Region

Japan


Condition

Condition

chronic fatigue syndrome

Classification by specialty

Psychosomatic Internal Medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To elucidate the effect of recumbent isometric yoga on severe patients with chronic fatigue syndrome.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

Before and after intervention period (12 weeks)
severity of fatigue
1) Chalder's fatigue scale score
2) POMS F score

Key secondary outcomes

Blood biomarkers such as DHEA-S, IFNg, IL-6 etc, autonomic nervous function, surface body temperature, fMRI.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Other

Interventions/Control_1

standard pharmacotherapy

Interventions/Control_2

pharmacotherapy + 20 min/day, daily recumbent isometric yoga

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

70 years-old >

Gender

Male and Female

Key inclusion criteria

Subjects were outpatients with CFS who visited the Department of Psychosomatic Medicine of Kyushu University Hospital who didn't recover satisfactory in spite of the treatments for at least 6 months.

Key exclusion criteria

Patients were excluded if their fatigue was due to physical disease such as liver, kidney, heart, respiratory, endocrine, autoimmune, or malignant disease, severe anemia, electrolyte abnormalities, obesity, or pregnancy.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Nobuyuki Sudo

Organization

Graduate School of Medical Sciences, Kyushu University

Division name

Department of Psychosomatic Medicine

Zip code


Address

Maidashi 3-1-1. Higashi-ku, Fukuoka

TEL

092-642-5323

Email

oka-t@cephal.med.kyushu-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Takakazu Oka

Organization

Graduate School of Medical Sciences, Kyushu University

Division name

Department of Psychosomatic Medicine

Zip code


Address

Maidashi 3-1-1. Higashi-ku, Fukuoka

TEL

092-642-5323

Homepage URL


Email

oka-t@cephal.med.kyushu-u.ac.jp


Sponsor or person

Institute

AMED

Institute

Department

Personal name



Funding Source

Organization

AMED

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


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

九州大学病院


Other administrative information

Date of disclosure of the study information

2016 Year 08 Month 04 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

Completed

Date of protocol fixation

2015 Year 12 Month 31 Day

Date of IRB


Anticipated trial start date

2016 Year 05 Month 12 Day

Last follow-up date

2018 Year 01 Month 31 Day

Date of closure to data entry

2018 Year 01 Month 31 Day

Date trial data considered complete


Date analysis concluded

2018 Year 09 Month 30 Day


Other

Other related information



Management information

Registered date

2016 Year 08 Month 04 Day

Last modified on

2018 Year 02 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000027039


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name