UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000057529
Receipt number R000065727
Scientific Title Transition of cancer survivors diagnosed with hereditary tumors
Date of disclosure of the study information 2026/04/01
Last modified on 2025/04/06 10:52:03

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Basic information

Public title

Transition of cancer survivors diagnosed with hereditary tumors

Acronym

Transition of cancer survivors diagnosed with hereditary tumors

Scientific Title

Transition of cancer survivors diagnosed with hereditary tumors

Scientific Title:Acronym

Transition of cancer survivors diagnosed with hereditary tumors

Region

Japan


Condition

Condition

Cancer

Classification by specialty

Nursing

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Identify transitions of cancer survivors diagnosed with hereditary tumors

Basic objectives2

Others

Basic objectives -Others

Examine supports to promote psychological adjustment for cancer survivors diagnosed with hereditary tumors

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Non

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1) The patient has been diagnosed with cancer and more than 4 months have passed since the completion of anticancer drug treatment, surgery, or radiation therapy.
2) The patient has been diagnosed with a hereditary tumor based on a genetic test or clinical diagnosis after being diagnosed with cancer, and it has been less than 6 years since the diagnosis of hereditary tumor.
3) The patient is able to speak Japanese and is aware that he/she is physically able to meet in person or online for a one-hour interview.

Key exclusion criteria

Non

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Satoko
Middle name
Last name MIYAWAKI

Organization

University of Kochi

Division name

Doctoral Program

Zip code

7910280

Address

160 Minamiumemoto-cho Kou Matsuyama-Shi Ehime

TEL

09048947649

Email

sattinlovesminmin@yahoo.co.jp


Public contact

Name of contact person

1st name Satoko
Middle name
Last name MIYAWAKI

Organization

Shikoku Cancer Center

Division name

Nursing-Dep

Zip code

7910280

Address

160 Minamiumemoto-cho Kou Matsuyama-Shi Ehime-pre

TEL

09048947649

Homepage URL


Email

sattinlovesminmin@yahoo.co.jp


Sponsor or person

Institute

MIYAWAKI Satoko

Institute

Department

Personal name



Funding Source

Organization

Non

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

University of Kochi

Address

2751-1 Ike Kochi-shi KOCHI

Tel

088-847-8700

Email

sattinlovesminmin@yahoo.co.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

2026 Year 04 Month 01 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

18

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

2022 Year 05 Month 26 Day

Date of IRB

2022 Year 04 Month 10 Day

Anticipated trial start date

2022 Year 06 Month 01 Day

Last follow-up date

2025 Year 03 Month 20 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Interview


Management information

Registered date

2025 Year 04 Month 06 Day

Last modified on

2025 Year 04 Month 06 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000065727