ClinicalTrials.gg
RecruitingNCT06773338Updated Jan 14, 2025

The Impact of Playing Tetris on Migrants' Mental Health

An interventional study of Tetris and No intervention in Post-traumatic Stress Disorder (PTSD), Anxiety Symptoms and Depression Symptoms, sponsored by Tilburg University. Recruiting at 2 sites in 2 countries. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-01-14.

Sponsored by Tilburg University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 11 months ago, but the record still lists the study as recruiting.
  • Started Dec 2024; still recruiting 1 year 10 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study examines if playing Tetris prevents the development of Post-traumatic stress disorder or related anxiety and depressive symptoms. The investigators recruit 300 participants in total in Greece and in the Netherlands. The participants are immigrants who have applied for asylum at any point in the past. The participants are asked to answer three questionnaires (on Post-traumatic stress disorder, related anxiety and depressive symptoms, and post-migration living difficulties) on a recurring basis - once every 4 weeks, 12 times in total. Half of the participants (treatment group) are randomly selected to play Tetris after completing the questionnaires. Participants in the treatment group are instructed to play Tetris for at least 15 minutes while trying to remember bad things that recently happened to them. Tetris is administered at three instances and participants in the treatment group are encouraged to play Tetris in case of experiencing any traumatic events or having any intrusive memories during the course of the study.

02

Conditions studied

  • Post-traumatic Stress Disorder (PTSD)
  • Anxiety Symptoms
  • Depression Symptoms

Keywords

  • Post-traumatic stress disorder
  • PTSD
  • Anxiety
  • Depression
  • Refugees
  • Asylum seekers
  • Migrants
  • Tetris
  • Longitudinal
03

In context

Stress Disorders, Post-Traumatic

2,682 studies on the registry are indexed under Stress Disorders, Post-Traumatic; 601 are open to participants now.

This study's planned enrollment of 300 is above the median of 69 across 2,196 interventional studies indexed under Stress Disorders, Post-Traumatic.

Browse Stress Disorders, Post-Traumatic studies →

Lead sponsor

Tilburg University is the lead sponsor of 27 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Arabic-speaking immigrants of any gender who have applied for asylum in Greece or in the Netherlands, regardless of the outcome of their asylum application and their current residency status (rejected asylum seekers, recognized refugees, undocumented migrants).

Exclusion criteria

Exclusion Criteria:

  • Minors (under the age of 18).
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
300 participants (estimated)

Study arms

  • Other
    Treatment tetris group

    Randomly selected participants who reply to mental health and migration-related difficulties questionnaires are asked to play Tetris during the research.

    Behavioral: Tetris

  • Other
    Control group

    Randomly selected participants who reply to mental health and migration-related difficulties questionnaires, but do not play Tetris during the research.

    Other: No intervention

Interventions

  • BehavioralTetris

    Randomly selected participants (migrants) are asked to play Tetris for at least 15 minutes on several occasions. These participants are asked while playing Tetris to try and remember bad events that recently happened to them. The participants play the classic version of the Tetris game directly on their mobile phone.

  • OtherNo intervention

    Participants do not receive any intervention.

06

What researchers measure

Primary outcomes

  1. Post-traumatic stress disorder

    The investigators use the Primary Care Post-Traumatic Stress Disorder Screen for Diagnostic and Statistical Manual of Mental Disorders fifth edition (PC-PTSD-5)

    Time frame: From enrolment to the end of the study (40 weeks)

  2. Anxiety and depression symptoms

    The investigators use the Kessler Psychological Distress Scale

    Time frame: From enrolment to the end of the study (40 weeks)

Secondary outcomes

  1. Post-migration living difficulties

    In the course of the study, the investigators measure variation in post-migration living difficulties such as separation from family, social isolation, language barriers, etc. Participants are presented a checklist of items and asked to identify for each item if it has been a problem for them over the last month, with 4 possible answers for each item: 1) not a problem; 2) minor problem; 3) serious problem; 4) very serious problem. In addition, participants are asked if over the last month they have 1) been victimised in any way ; 2) had any negative experiences involving bureaucratic personnel or state officials; 3) had experiences that made them feel happy and gave them hope for the future (open questions).

    Time frame: From enrolment to the end of the study (40 weeks)

07

Study locations

1 of 2 sites recruiting
  • Upinion (online)
    The Hague, NL 2511 CJ, Greece
    Not yet recruiting
  • Upinion/the humanity Hub
    The Hague, NL 2511 CJ, Netherlands
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — In accordance with Tilburg University's standards and considering the sensitivity of the data collected from asylum seekers, the availability for reuse of the data will be subject to careful consideration and protection of privacy. The availability of the data for reuse will be determined on a case-by-case basis, taking into consideration the consent obtained from participants, any legal or ethical restrictions, and the level of identifiability of the data. To protect the privacy and confidentiality of the asylum seekers, data sharing will be done in a controlled manner.The availability of the data for reuse will be determined on a case-by-case basis, taking into consideration the consent obtained from participants, any legal or ethical restrictions, and the level of identifiability of the data.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 14, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06773338
Lead sponsor
Tilburg University
Collaborators
Stichting tot steun VCVGZ
Responsible party
Mario Braakman (Professor, Tilburg University) — Principal investigator
First posted
Jan 14, 2025
Start date
Dec 17, 2024
Primary completion
Dec 7, 2025 (estimated)
Completion
Dec 7, 2025 (estimated)
Last update
Jan 14, 2025

Study contacts

Mario Braakman, Prof.
Contact
Mario.Braakman@tilburguniversity.edu
+31629514366
Tihomir Sabchev, Dr.
Contact
t.y.sabchev@tilburguniversity.edu

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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