UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000037682
Receipt number R000042792
Scientific Title Effects of renal rehabilitation on motor function in home facilities for patients with pre-dialysis CKD and home hemodialysis
Date of disclosure of the study information 2019/09/01
Last modified on 2019/08/20 13:17:11

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Basic information

Public title

Effects of renal rehabilitation on motor function in home facilities for patients with pre-dialysis CKD and home hemodialysis

Acronym

Effects of renal rehabilitation on motor function in home facilities for patients with pre-dialysis CKD and home hemodialysis

Scientific Title

Effects of renal rehabilitation on motor function in home facilities for patients with pre-dialysis CKD and home hemodialysis

Scientific Title:Acronym

Effects of renal rehabilitation on motor function in home facilities for patients with pre-dialysis CKD and home hemodialysis

Region

Japan


Condition

Condition

choronic renal disease

Classification by specialty

Nephrology Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of the study was to examine the improvement effect of exercise function by renal rehabilitation in patients with with pre-dialysis chronic kidney disease and in home hemodialysis patients at home facilities.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Others

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

Exercise functions are evaluated by 6 minutes walking, Time "Up and Go" test, normal walking speed, maximum walking speed, 30 seconds sitting, 5 times sitting before and 1, 3, 6 months after renal rehabilitation.

Key secondary outcomes

Muscle mass (grip strength, large chest muscle strength, quadriceps femoris muscle strength), physical findings (body weight, cardiothoracic ratio), ADL (Functional Independence Measure) and blood data (blood hemoglobin concentration, serum albumin concentration, Kt / V, nPCR Evaluate) are evaluated before and 1, 3, 6 months after renal rehabilitation. At the same time, renal functions (blood urea nitrogen, creatinine, glomerular filtration rate, urinary protein) are evaluated in pre-dialysis chronic kidney disease patients.


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

Among the residents in Medical Home Fujimino, we will carry out kidney rehabilitation for patients with chronic kidney disease patients not on dialysis (5 patients) and home hemodialysis patients (10 patients) who agreed to perform renal rehabilitation.

Key exclusion criteria

Hemodialysis patients are excluded from this study when they discontinue dialysis, transition to peritoneal dialysis, combined with peritoneal dialysis, or receive kidney transplantation.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Akira
Middle name
Last name Tsuji

Organization

Fuke Home Medical Rehabilitation Care Center

Division name

Medical division

Zip code

356-0051

Address

1839-4 Kamekubo, Fujimino Saitama, Japan

TEL

049-293-8222

Email

atsuji@fukekai.com


Public contact

Name of contact person

1st name Akira
Middle name
Last name Tsuji

Organization

Fuke Rehabilitation Home Care Center

Division name

Medical division

Zip code

356-0051

Address

1839-4 Kamekubo, Fujimino Saitama, Japan

TEL

049-293-8222

Homepage URL

http://www.fuke-zaitaku.com/

Email

atsuji@fukekai.com


Sponsor or person

Institute

Fuke Rehabilitation Home Care Center
Medical division

Institute

Department

Personal name



Funding Source

Organization

Fuke hospital

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethical Committee of Fuke hospital

Address

2197 Kamekubo, Fujimino Saitama, Japan

Tel

049-264-8811

Email

t-futaesaku@fukekai.com


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

富家在宅リハビリテーションケアセンター / Fuke Home Medical Rehabilitation Care Center


Other administrative information

Date of disclosure of the study information

2019 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

Enrolling by invitation

Date of protocol fixation

2019 Year 07 Month 25 Day

Date of IRB

2019 Year 08 Month 14 Day

Anticipated trial start date

2019 Year 09 Month 01 Day

Last follow-up date

2020 Year 08 Month 31 Day

Date of closure to data entry

2021 Year 04 Month 01 Day

Date trial data considered complete

2021 Year 07 Month 01 Day

Date analysis concluded

2021 Year 08 Month 31 Day


Other

Other related information

This is the observational study of cases. The subjects are 10 pre-dialysis CKD patients and 10 home hemodialysis patients who lived in Medical Home Fujimino from September 2019 to March 2020. The exercise programs consist of (1) Stretching the extremities trunk (2) Aerobic exercise (walking or ergometer, Borg scale 11 to 13 intensity for 20-60 minutes) A physical therapist drafts an individual program (set / day) and implements it three days a week (partly supervised twice, once self-managed). The items to be measured are 6 minutes walking for motor function, Time "Up and Go" test, normal walking speed, maximum walking speed, 30 seconds standing and sitting 5 times before study and after 1, 3 and 6 months.


Management information

Registered date

2019 Year 08 Month 14 Day

Last modified on

2019 Year 08 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042792


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name