UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000055816
Receipt number R000063774
Scientific Title Evaluating the effectiveness of support program for parents of children with school refusal
Date of disclosure of the study information 2024/10/15
Last modified on 2025/10/15 11:55:46

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Basic information

Public title

Evaluating the effectiveness of support program for parents of children with school refusal

Acronym

Effectiveness of support program for parents of children with school refusal

Scientific Title

Evaluating the effectiveness of support program for parents of children with school refusal

Scientific Title:Acronym

Effectiveness of support program for parents of children with school refusal

Region

Japan


Condition

Condition

Parents of children with school refusal

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to implement the support programs for parents of child with school refusal and evaluate its effectiveness as an indicator of improvement in parental mental health.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Patient Health Questionnaire-9 (PHQ-9) (9 items)

Key secondary outcomes

Positive and negative parenting scale (PNPS) (24 items)
Parenting self-efficacy scale (PSE) (14 items)
Strength and difficulties questionnaire (SDQ) (24 items)
Number of days a child was absent from school (2 items)


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Other

Interventions/Control_1

Participants in the support program for parents of children with school refusal. A support program consisting of six 90-minute sessions per session will be implemented with a two-week interval between each session.

Interventions/Control_2

Participants in the roundtable discussion for parents of children with school refusal. Not implemented since there were no requests to participate in the support program.

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Individuals who understand the purpose of the study and agree to participate in the study.
Native speakers of Japanese and those who can fill in the questionnaire.
Participants in the support program for parents of children with school refusal.
One-time participants in a roundtable discussion for parents of children with school refusal.

Key exclusion criteria

N/A.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Akemi
Middle name
Last name Okumura

Organization

Hamamatsu University School of Medicine

Division name

Research Center for Child Mental Development

Zip code

431-3192

Address

1-20-1 Handayama, Chuo-ku, Hamamatsu, Japan

TEL

053-435-2331

Email

okumura@hama-med.ac.jp


Public contact

Name of contact person

1st name Akemi
Middle name
Last name Okumura

Organization

Hamamatsu University School of Medicine

Division name

Research Center for Child Mental Development

Zip code

431-3192

Address

1-20-1 Handayama, Chuo-ku, Hamamatsu, Japan

TEL

053-435-2331

Homepage URL


Email

okumura@hama-med.ac.jp


Sponsor or person

Institute

Hamamatsu University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Hamamatsu 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

Hamamatsu University School of Medicine

Address

1-20-1 Handayama, Chuo-ku, Hamamatsu, Japan

Tel

053-435-2680

Email

rinri@hama-med.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

2024 Year 10 Month 15 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

39

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

2024 Year 05 Month 15 Day

Date of IRB

2024 Year 08 Month 02 Day

Anticipated trial start date

2024 Year 09 Month 30 Day

Last follow-up date

2025 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2024 Year 10 Month 11 Day

Last modified on

2025 Year 10 Month 15 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063774