UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000062282
Receipt number R000071276
Scientific Title Effects of an outing-promotion intervention on behavioral and psychological symptoms of dementia (BPSD) among group home residents: a facility-stratified, pair-matched, randomized controlled trial
Date of disclosure of the study information 2026/07/20
Last modified on 2026/07/20 21:48:34

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Basic information

Public title


Effects of an outing-promotion intervention on behavioral and psychological symptoms of dementia (BPSD) among group home residents: a facility-stratified, pair-matched, randomized controlled trial

Acronym

Outing promotion for BPSD reduction trial

Scientific Title


Effects of an outing-promotion intervention on behavioral and psychological symptoms of dementia (BPSD) among group home residents: a facility-stratified, pair-matched, randomized controlled trial

Scientific Title:Acronym

Outing promotion for BPSD reduction trial

Region

Japan


Condition

Condition

Dementia

Classification by specialty

Geriatrics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the effects of a staff-delivered outing-promotion intervention on the occurrence of behavioral and psychological symptoms of dementia (BPSD) among residents of group homes, using a randomized controlled design, and to evaluate the trajectory of BPSD occurrence during the post-intervention observation period.

Basic objectives2

Others

Basic objectives -Others

Verification of the effectiveness of a non-pharmacological intervention and exploration of the trajectory of effects after intervention discontinuation

Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

BPSD occurrence rate derived from routine care records (weekly proportion of resident-days with documented BPSD). Assessment: operational baseline period (May 15-31, 2025) and post-baseline period (June 1 to December 31, 2025).

Key secondary outcomes

Outing rate (weekly proportion of resident-days with documented outings; adherence measure)
Change in Hasegawa Dementia Scale-Revised (HDS-R) scores (t1 to t2)
Trajectory of BPSD occurrence and between-group differences during the post-intervention observation period (January 1 to May 31, 2026)


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification

YES

Dynamic allocation

NO

Institution consideration

Institution is considered as a block.

Blocking

YES

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

Intervention group: Outing promotion. Care staff actively encouraged residents to go outdoors (walks, shopping, outdoor activities, etc.). The intervention period was from May 15 to December 31, 2025. The intervention was discontinued from January 1, 2026, followed by an observation period under usual care. Because an electronic care-record system was introduced simultaneously with the start of the intervention, no pre-intervention record data exist; the first two weeks of the intervention period (May 15 to 31, 2025) were defined as the operational baseline.

Interventions/Control_2

Control group: Usual care without specific outing promotion.

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

Residents with dementia living in the three participating group home units (dementia group homes) as of April 2025.

Key exclusion criteria

Residents with planned discharge at the time of allocation, etc.

Target sample size

24


Research contact person

Name of lead principal investigator

1st name Koji
Middle name
Last name Hara

Organization

Yokohama City University

Division name

School of Economics and Business Administration

Zip code

2360027

Address

22-2 Seto, Kanazawa-ku, Yokohama, Kanagawa, Japan

TEL

0457872131

Email

hara.koj.vv@yokohama-cu.ac.jp


Public contact

Name of contact person

1st name Koji
Middle name
Last name Hara

Organization

Yokohama City University

Division name

School of Economics and Business Administration

Zip code

2360027

Address

22-2 Seto, Kanazawa-ku, Yokohama, Kanagawa, Japan

TEL

0457872131

Homepage URL


Email

hara.koj.vv@yokohama-cu.ac.jp


Sponsor or person

Institute

Yokohama City University

Institute

Department

Personal name

Koji Hara


Funding Source

Organization

Other

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Research Ethics Committee of the Hakkei Campus, Yokohama City University

Address

22-2 Seto, Kanazawa-ku, Yokohama, Kanagawa, Japan

Tel

045-787-2354

Email

sangaku@yokohama-cu.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

認知症対応型共同生活介護事業所3施設(非公開)


Other administrative information

Date of disclosure of the study information

2026 Year 07 Month 20 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

24

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

2025 Year 04 Month 19 Day

Date of IRB

2025 Year 04 Month 07 Day

Anticipated trial start date

2025 Year 05 Month 15 Day

Last follow-up date

2026 Year 05 Month 31 Day

Date of closure to data entry

2026 Year 05 Month 31 Day

Date trial data considered complete

2026 Year 08 Month 31 Day

Date analysis concluded

2026 Year 09 Month 30 Day


Other

Other related information

This trial was registered retrospectively because the principal investigator was not fully aware of the trial registration requirement at study initiation. Allocation was performed on April 19, 2025, and the procedure is preserved as a dated internal document. The primary outcome and analysis approach were described in the interim analysis report of January 2026. Following the interim analysis based on care records during the intervention period (May to December 2025), the intervention was discontinued in January 2026, and observation under usual care has continued thereafter.


Management information

Registered date

2026 Year 07 Month 20 Day

Last modified on

2026 Year 07 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000071276