UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000047216
Receipt number R000053855
Scientific Title Effects of cognitive behavioral therapy combined with exercise therapy on the physical activity of older adults with dynapenia: a randomized controlled trial
Date of disclosure of the study information 2022/03/18
Last modified on 2023/06/21 13:19:08

* 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

Effectiveness of Cognitive Behavioral Therapy combined with Exercise Therapy on the Improving Physical Activity of Older Adults with Dynapenia

Acronym

Clinical study on improvement of physical activity in older adults with dynapenia

Scientific Title

Effects of cognitive behavioral therapy combined with exercise therapy on the physical activity of older adults with dynapenia: a randomized controlled trial

Scientific Title:Acronym

Effects of CBT combined with exercise therapy on the physical activity of older adults with dynapenia: RCT

Region

Japan


Condition

Condition

Dynapenia(including sarcopneia)

Classification by specialty

Geriatrics Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To determine if there is a difference in change in physical activity in community-dwelling older adults with dynapenia (including sarcopenia) with and without combined therapy (cognitive behavioral therapy, exercise therapy, and health education)

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Change in total physical activity measured by IPAQ

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation

YES

Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

Combination cognitive-behavioral therapy, exercise therapy, and health education

Interventions/Control_2

waiting-list

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) 65 years old or older
2) Reside in Tsukumi City
3) Grip strength is less than 28 kg for men and less than 18 kg for women.
4) Able to walk on their own or with the use of a walking aid (cane, walker, etc.)
5) Able to communicate, read and write in Japanese
6) Understand the content of this study and give written consent to participate in the study of their own free will.

Key exclusion criteria

1) Cognitive function is impaired (as measured by Mini-Mental State Examination).

2) Exercise is prohibited by the family physician for medical reasons.

Target sample size

140


Research contact person

Name of lead principal investigator

1st name Eishi
Middle name
Last name Miyazaki

Organization

Oita University Medical School Hospital

Division name

department of general medicine

Zip code

879-5593

Address

1-1, Idaigaoka 1-chome, Hasama-cho, Yufu City, Oita Prefecture

TEL

097-586-5106

Email

eishida@oita-u.ac.jp


Public contact

Name of contact person

1st name Noboru
Middle name
Last name Horinouchi

Organization

Oita University Medical School Hospital

Division name

department of general medicine

Zip code

879-5593

Address

1-1, Idaigaoka 1-chome, Hasama-cho, Yufu City, Oita Prefecture

TEL

097-586-5106

Homepage URL


Email

nhorinouchi@oita-u.ac.jp


Sponsor or person

Institute

Oita University Medical School Hospital department of general medicine

Institute

Department

Personal name



Funding Source

Organization

Department of General Medicine, Oita University School of Medicine

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Interventional Clinical Research Review Committee, Oita University School of Medicine

Address

1-1, Idaigaoka 1-chome, Hasama-cho, Yufu City, Oita Prefecture

Tel

097-586-6163

Email

gcrcjimu@oita-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



Other administrative information

Date of disclosure of the study information

2022 Year 03 Month 18 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

Terminated

Date of protocol fixation

2022 Year 03 Month 18 Day

Date of IRB

2022 Year 04 Month 27 Day

Anticipated trial start date

2022 Year 04 Month 27 Day

Last follow-up date

2025 Year 04 Month 27 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2022 Year 03 Month 18 Day

Last modified on

2023 Year 06 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000053855