UMIN-CTR Clinical Trial

Recruitment status Completed
Unique ID issued by UMIN UMIN000011171
Receipt No. R000013018
Scientific Title Pilot Study for ORAl myofunctional CLinical Evidence: elderly
Date of disclosure of the study information 2013/07/11
Last modified on 2019/09/29 (Ver. 9)

* 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 Pilot Study for ORAl myofunctional CLinical Evidence: elderly
Acronym ORACLE Pilot, TSUBAKI
Scientific Title Pilot Study for ORAl myofunctional CLinical Evidence: elderly
Scientific Title:Acronym ORACLE Pilot, TSUBAKI
Region
Japan

Condition
Condition Elders who need care
Classification by specialty
Geriatrics Rehabilitation medicine
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 To perform pilot study for creating evidence of oral myofunctional training in elders who need care in sleeping condition. To evaluate indicators from viewpoints of improving activities of daily living (ADL) and quality of life (QOL).
Basic objectives2 Efficacy
Basic objectives -Others
Trial characteristics_1 Exploratory
Trial characteristics_2 Pragmatic
Developmental phase Not applicable

Assessment
Primary outcomes Sleeping stage, apnea and hypopnea assessed by polysomnography
Key secondary outcomes Blood pressure, pulse, frequency of stool, height, weight, grip strength, functional independence measurement (FIM), Mini-Mental State (MMSE), GDS, depressive state (PHQ9), oral examination, amount of saliva, cardiovascular and other vascular events, death by all cause

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 Behavior,custom Maneuver
Interventions/Control_1 Oral myofunctional training program
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
65 years-old <=
Age-upper limit

Not applicable
Gender Male and Female
Key inclusion criteria 1) Person who lives or visits regularly in Social Welfare Corporation Tsubakigaoka, an Intensive Care Home for the Elderly.
2) Person whoare age from 65.
3) Person who is qualified as a Person Requiring Lon-Term Care.
Key exclusion criteria 1) Person who is mechanically-entilated.
2) Person who has serious conditions in the oral cavity
3) who is unable to obtain agreement.
Target sample size 13

Research contact person
Name of lead principal investigator
1st name Tomomi
Middle name
Last name Ide
Organization Kyushu University Hospital
Division name Department of Cardiovascular Medicine
Zip code 812-8582
Address 3-1-1, Maidashi, Higashi-ku, Fukuoka
TEL 81-92-642-5360
Email tomomi_i@cardiol.med.kyushu-u.ac.jp

Public contact
Name of contact person
1st name Tomomi
Middle name
Last name Ide
Organization Kyushu University
Division name Department of Cardiovascular Medicine
Zip code 812-8582
Address 3-1-1, Maidashi, Fukuoka
TEL 095-801-8023
Homepage URL
Email info@ffc-p.jp

Sponsor
Institute Kyushu University
Institute
Department

Funding Source
Organization None
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 Clinical Research Network Fukuoka
Address 3-1-1, Maidashi, Higashiku, Fukuoka
Tel 092-643-7171
Email mail@crnfukuoka.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 社会福祉法人椿ヶ丘特別養護老人ホーム椿ヶ丘荘

Other administrative information
Date of disclosure of the study information
2013 Year 07 Month 11 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
2013 Year 05 Month 31 Day
Date of IRB
Anticipated trial start date
2013 Year 07 Month 11 Day
Last follow-up date
2014 Year 02 Month 20 Day
Date of closure to data entry
2014 Year 06 Month 17 Day
Date trial data considered complete
2014 Year 06 Month 17 Day
Date analysis concluded
2014 Year 07 Month 29 Day

Other
Other related information

Management information
Registered date
2013 Year 07 Month 11 Day
Last modified on
2019 Year 09 Month 29 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000013018