UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000031075
Receipt number R000035489
Scientific Title Effects of remote feedback and self-monitoring intervention using pedometer on physical activity in patients with Parkinson's disease : A pilot study
Date of disclosure of the study information 2018/01/31
Last modified on 2022/02/03 10:06:43

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Basic information

Public title

Effects of remote feedback and self-monitoring intervention using pedometer on physical activity in patients with Parkinson's disease : A pilot study

Acronym

Effects of remote feedback and self-monitoring intervention on physical activity in patients with Parkinson's disease : A pilot study

Scientific Title

Effects of remote feedback and self-monitoring intervention using pedometer on physical activity in patients with Parkinson's disease : A pilot study

Scientific Title:Acronym

Effects of remote feedback and self-monitoring intervention on physical activity in patients with Parkinson's disease : A pilot study

Region

Japan


Condition

Condition

Parkinson's disease

Classification by specialty

Neurology Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The study tests the effects of remote feedback and self-management intervention on the physical activity, physical, mental function and Parkinson's symptoms in patients with Parkinson's diseases.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

(1) step counts at pre and post intervention (6 month)

Key secondary outcomes

(1) indicator of Parkinson's disease symptoms (motor symptoms, non-motor symptoms)
(2) drug regimen
(3) cognitive function (attention, executive function, processing speed, etc.)
(4) physical and mental performance and physical activity
(5) psychological outcomes
(6) daily life performance outcomes
(7) biomarker


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

Active

Stratification

YES

Dynamic allocation

NO

Institution consideration


Blocking

YES

Concealment

Central registration


Intervention

No. of arms

3

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Behavior,custom

Interventions/Control_1

Control group: once-monthly Provide educational information for 6 months

Interventions/Control_2

Feedback and self-monitoring group: once-monthly pedometer-based step counts goal setting (5% increase) program and Provide educational information for 6 months

Interventions/Control_3

Feedback and self-monitoring group: once-monthly pedometer-based step counts goal setting (10% increase) program and Provide educational information for 6 months

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


Not applicable

Gender

Male and Female

Key inclusion criteria

For those who meet all of the following
(1) Diagnosed as Parkinson's disease based on UK Parkinson's Disease Society Brain Bank criteria
(2) Stable antiparkinson drug regimen for at least 4 weeks prior to study entry
(3) Stages <=3 in the ON state for Modified Hoehn and Yahr Scale
(4) People who have given written consent

Key exclusion criteria

Exclude any person who also corresponds to one of the following
(1) History of severe neurological diseases such as dementia, visual impairment, psychiatric disorders
(2) Those who have severe cardiopulmonary disorder
(3) Walking in daily life is not independent
(4) People who are in the Investigator's judgment unlikely to comply with medical regimens or study requirements

Target sample size

45


Research contact person

Name of lead principal investigator

1st name Yoshio
Middle name
Last name Tsuboi

Organization

Fukuoka University

Division name

Department of Neurology

Zip code

814-0180

Address

7-45-1 Nanakuma, Jonan-ku, Fukuoka-city, Fukuoka, Japan

TEL

092-801-1011

Email

tsuboi@cis.fukuoka-u.ac.jp


Public contact

Name of contact person

1st name Koichi
Middle name
Last name Nagaki

Organization

Fukuoka University Graduate School of Medicine

Division name

Department of Neurology and Neurological Science

Zip code

814-0180

Address

7-45-1 Nanakuma, Jonan-ku, Fukuoka-city, Fukuoka, Japan

TEL

092-801-1011

Homepage URL


Email

nagaki.fukuoka.university@gmail.com


Sponsor or person

Institute

Department of Neurology, Fukuoka university

Institute

Department

Personal name



Funding Source

Organization

Fukuoka University

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

Fukuoka university Review Board

Address

7-45-1 Nanakuma, Jonan-ku, Fukuoka-city, Fukuoka, Japan

Tel

092-801-1011

Email

fu-merb-bigvan@fukuoka-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

福岡大学病院(福岡県)


Other administrative information

Date of disclosure of the study information

2018 Year 01 Month 31 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

No longer recruiting

Date of protocol fixation

2018 Year 01 Month 17 Day

Date of IRB

2018 Year 01 Month 17 Day

Anticipated trial start date

2018 Year 02 Month 01 Day

Last follow-up date

2018 Year 11 Month 30 Day

Date of closure to data entry

2018 Year 12 Month 31 Day

Date trial data considered complete

2023 Year 03 Month 31 Day

Date analysis concluded

2023 Year 03 Month 31 Day


Other

Other related information



Management information

Registered date

2018 Year 01 Month 31 Day

Last modified on

2022 Year 02 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000035489


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name