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A Computer Game for Postpartum Mental Health After Emergency Cesarean Birth

NCT07290127 · tracked via the Priya Life Science Japan tracker
Sponsor
Kyoto University, Graduate School of Medicine
Phase
Not applicable
Started
2025-12-13
Last updated
2025-12-18

Condition(s) studied

Post-traumatic Stress Disorder (PTSD)Postpartum Mental Health

Investigational drug(s) / intervention(s)

implementation of a brief computer-based intervention "Tetris"

implementation of a brief computer-based intervention "Tetris": Within 24 hours of emergency caesarean birth, the participants played Tetris (TetrisⓇ99), a cognitive task, for at least 10 and up to 15 minutes on a Nintendo Switch Lite game console.

Study summary

This study aims to explore whether playing the computer game Tetris can reduce PTSD symptoms in women who have undergone emergency caesarean births. Additionally, as a feasibility study, it seeks to provide essential data and insights that will guide the design and implementation of future larger-scale RCTs examining the effects of Tetris in this context.

The specific objectives are to explore:

1. Whether playing Tetris within 24 hours of an emergency C-section help to reduce symptoms of PTSD.
2. Clinical feasibility and acceptability for an intervention (ie. game Tetris) immediately after a cesarean section.
3. Issues arising from the research design, including requitement and sample size.

Participants in the intervention group will play Tetris for at least 10 minutes, but no more than 15 minutes within 24 hours of a C-section.

For outcomes, all participants will complete the questionnaires on the fifth day after the C-section and one month postpartum.

Eligibility

Sex
FEMALE
Min age
20 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Women aged 20 years or older * Women who have undergone an emergency caesarean birth within the previous 24 hours * Must be able to understand instructions and respond to the questionnaire in Japanese Exclusion Criteria: * Undergoing treatment for psychiatric disorders such as PTSD, depression, anxiety disorders or schizophrenia. * Undergoing intensive care after surgery . * The physician does not approve participation for any physical or mental reasons .

Primary outcome measure(s)

  • Impact of Event Scale-Revised (IES-R) scores (intrusive, avoidance and total scores) at one month postpartum — At one month postpartum
    The participants are asked to report the degree of distress experienced for each item in the past 7 days. The 5 points on the scale are: 0 (not at all), 1 (a little bit), 2 (moderately), 3 (quite a bit), 4 = (extremely).

Trial sites (1)

FacilityCityRegionStatus
Perinatal epidemiology Department of Human Health Sciences Graduate School of Medicine Kyoto University Kyoto Sakyo-ku

More Kyoto University, Graduate School of Medicine trials in Japan

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07290127 on ClinicalTrials.gov ↗ ← All trials in Japan