Tokyo, July 21 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000062284) titled 'A Feasibility Study of Imagery Rescripting Drawing Therapy' on July 20.
Study Type:
Interventional
Study Design:
Basic Design - Single arm
Randomization - Non-randomized
Blinding - Open -no one is blinded
Control - Uncontrolled
Primary Sponsor:
Institute - Chiba University
Condition:
Condition - Subjective distress from adverse memories (Healthy volunteers)
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To investigate the feasibility of a novel approach, Image Rescriptingand Drawing Therapy (IRDT), delivered in an online setting for healthyadults with distressing memories.
Basic objectives2 - Safety
Intervention:
Interventions/Control_1 - Imagery Rescripting Drawing Therapy (IRDT). All participants will be provided with an iPad and a designated pen free of charge, and will receive "Imagery Rescripting Drawing Therapy (IRDT)" online via a web conferencing system. The intervention will be conducted once a week (60 minutes each) for a total of 3 sessions.
Eligibility:
Age-lower limit - 18
years-old
=
Gender - Male and Female
Key inclusion criteria - 1.Aged between 18 and 65 years.
2.Not currently undergoing treatment for any mental or physical illness.
3.Having experienced an adverse event in the past, with a Visual Analogue Scale (VAS) subjective distress score (out of 100) of 30 or higher, and wishing for alleviation through online drawing therapy.
4.Having an internet environment (computer, tablet, or smartphone).
5.Capable of understanding the explanation in Japanese and providing free and voluntary consent via a web conferencing system.
Key exclusion criteria - 1.History of diagnosis of any mental disorder, such as schizophrenia, bipolar disorder, depression, or alcohol dependence.
2.Currently taking medication (including herbal medicines and supplements) for mental health issues.
3.Having experiences strongly suspected of being PTSD or acute stress disorder.
Having suicidal ideation (score of 2 or higher on question 9 of the PHQ-9).
5.Judged by the principal investigator or co-investigators as inappropriate to safely conduct this study.
Target Size - 3
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2026 Year 06 Month 01 Day
Anticipated trial start date - 2026 Year 07 Month 16 Day
Last follow-up date - 2026 Year 08 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000071193
Disclaimer: Curated by HT Syndication.
