Skip to content

Simple Cognitive Task Intervention After Trauma During COVID-19 In Hospital Staff EKUT-P RCT

Reducing Intrusive Memories After Trauma Via a Simple Cognitive Intervention During COVID-19 in Hospital Staff: EKUT-P (Enkel Kognitiv Uppgift Efter Trauma Under COVID-19 - sjukvårdspersonal) - A Randomized Controlled Trial (RCT)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04460014
Enrollment
164
Registered
2020-07-07
Start date
2020-09-30
Completion date
2022-10-31
Last updated
2022-11-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intrusive Memories of Traumatic Event(s), Post Traumatic Stress Disorder

Keywords

Post Traumatic Stress Disorder, Digital Intervention, Intrusive Memories of Traumatic Event(s)

Brief summary

This research study is designed to investigate the effects of a remotely delivered simple cognitive task (a memory cue followed by playing the computer game Tetris with mental rotation instructions) on intrusive memories (flashbacks) and other symptoms after a traumatic event(s). Hospital staff who experienced a work-related traumatic event(s) during the COVID-19 pandemic will be randomly allocated to either the simple cognitive task intervention or control. Randomization to assigned intervention occurs on Day 1, after completion of baseline measures (note: baseline measures are not used in randomization process). Baseline measures include questionnaires on Day 1 and an intrusive memory diary during the previous week (Week 0). Participants will be followed up at one week and one month, and where possible 3 and 6 months. It is predicted that participants given the simple cognitive task intervention will develop fewer intrusive memories, less severe related clinical symptoms, and will show higher functioning (e.g. at work) than those who are not. This will inform the future development of a simple technique to prevent distressing psychological symptoms after a traumatic event(s). Implementation and training aspects regarding remote recruitment and intervention delivery in a hospital context will also be explored. Participants use e.g. their smartphone for part of the intervention in the study.

Detailed description

This is a Randomised Controlled Trial informed by prior feasibility and pilot work (ClinicalTrials.gov IDs: NCT03509792, NCT04185155). The primary outcome is the number of intrusive memories of the traumatic event(s) (week 5). The intervention is delivered remotely (e.g. via smartphone) with potential remote support (e.g. by phone) to medical staff in Swedish hospitals.

Interventions

Session 1: A memory cue followed by playing the computer game Tetris (e.g. on own smartphone) with mental rotation instructions. Options to engage in self-administered/guided booster sessions per intrusive memory.

Session 1: Digital activity for same amount of time (e.g. listening to podcast on own smartphone).

Sponsors

Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 18 or over * Clinical work during the COVID-19 pandemic in hospital and care facilities (e.g. ICU, ambulance, intermediate care, ward) * Experienced at least one traumatic event in relation to their clinical work as health care staff during the COVID-19 pandemic * This/these event(s) at work meet(s) the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM5) criterion A for Posttraumatic Stress Disorder (PTSD): exposure to actual or threatened death, serious injury, or sexual violence by Directly experiencing the traumatic event(s) or Witnessing, in person, the event(s) as it occurred to others * The traumatic event(s) occured since the start of the COVID-19 pandemic * Report memory of the accident * Fluent in spoken and written Swedish * Alert and orientated * Have sufficient physical mobility to use their smartphone * Willing and able to provide informed consent and complete study procedures * Willing and able to be contacted while the study is ongoing * Have access to an internet enabled smartphone * Experiences distressing intrusive memories (of a traumatic event in relation to their work as health care staff during the COVID-19 pandemic) * Has experienced at least two such intrusive memories of a work-related traumatic event during the week before inclusion/exclusion * Able and willing to briefly write down these intrusive memories (without going into any detail)

Exclusion criteria

* Loss of consciousness of \> 5 minutes in relation to the traumatic event * Current intoxication during the traumatic event or in relation to study inclusion

Design outcomes

Primary

MeasureTime frameDescription
Number of intrusive memories of traumatic event(s)Week 5Number of intrusive memories of traumatic event(s) recorded by participants in a brief diary daily (morning, afternoon, evening and night) for 7 days.

Secondary

MeasureTime frameDescription
Intrusion questionnaire - frequency itemBaseline (Day 1), Week 1 and 5 and 1, 3, and 6 month follow-upA single item measuring the frequency of intrusive/unwanted memories of the traumatic event(s) in the previous week on a 7-point scale (from never to many times a day, with a follow-up question to specify the number if necessary) that will be used as a convergent measure for medical hospital staff who may face time constraints completing the diary.
Intrusion questionnaire - characteristicsBaseline (Day 1), One week and 1, 3, and 6 month follow-up5 self-rated items measuring the characteristics of intrusive/unwanted memories in the previous week. The level of distress, nowness, reliving, disconnectedness and whether different triggers are associated with the intrusive/unwanted memories of the traumatic event(s) are measured on a 101-point scale (from 0 to 100). Higher scores indicate more intrusive/unwanted memories, higher levels of distress/nowness/reliving/disconnectedness and a greater number of different triggers.
Number of intrusive memories of traumatic event(s)Week 0 and Week 1Number of intrusive memories of traumatic event(s) recorded by participants in a brief diary daily (morning, afternoon, evening and night) for 7 days.
Posttraumatic Stress Disorder Checklist 5 (PCL-5) short versionBaseline (Day 1), One week and 1, 3, and 6 month follow-upThe PCL-5 short version is an 8-item self-report measure that assesses current symptoms of post-traumatic stress disorder in the last month \[Baseline (Day 1), 1, 3, and 6 month follow-up\] and in the last week (One week). Items are rated on a 5-point scale ranging from 0 (not at all) to 4 (extremely). The PCL-5 short version yields a total symptom severity score which ranges from 0 to 32. Subscale symptom severity scores for DSM-5 symptom cluster B - intrusion symptoms (items 1-2), cluster C - avoidance (items 3-4), cluster D - negative alterations in cognitions and mood (items 5-6), and cluster E - alterations in arousal and reactivity (items 7-8). Higher scores indicate worse severity.
Characteristics of intrusive trauma memoriesBaseline (Day 1), Week 1 and week 52 self-rated items measuring the level of distress and vividness associated with the intrusions (11 point scales from 0 to 10) rated within the diary at baseline (Day 1), week 1 and week 5. High scores indicate higher level of distress/vividness.
Impact of Event Scale - Revised (IES-R): Degree of subjective distress of post-trauma intrusion and avoidance symptomsBaseline (Day 1), One week and 1, 3, and 6 month follow-upSelf-report measure that assesses subjective distress after a traumatic event (with reference to study event\[s\]) in the last week. Here we include the intrusion subscale (8 items) and the avoidance subscale (8 items). Items are rated on a 5-point scale ranging from 0 (not at all) to 4 (extremely). Subscale scores are calculated for the Intrusion or Avoidance items summed (ranging from 0 to 32 each). Higher scores indicate worse outcome.

Other

MeasureTime frameDescription
Sick leaveBaseline (Day 1), One week, 1, 3, and 6 month follow-up2 bespoke items measuring the total number and the number of full work days on sick leave because of reason for seeking health care. Higher numbers indicate more sick leave.
Stress and Energy Questionnaire (SEQ) - Stress subscaleBaseline (Day 1), One week, 1, 3, and 6 month follow-up3 items measuring the frequency of feeling stressed, pressured, tensed at work during the previous week on a 5-point scale (from never to several times per day). Item scores are summed. Higher scores indicate higher levels of stress. Further, a single item measuring difficulties to let go of work-related thoughts during leisure time (from very rarely or never to very often or always) and a single question about whether the above mentioned difficulties are because of intrusive memories with a yes/no response.
Scale of Work Engagement and Burnout (SWEBO) - Burnout subscaleBaseline (Day 1) and 6 month follow-up9 self-report items (4-point scale from 1 not at all to 4 all the time) measuring symptoms of burnout on three subscales: Exhaustion (items 1-3), disengagement (items 4-6) and inattentiveness (items 7-9). Subscale scores will be the mean of all items per subscale, the total burnout score will be the mean of all items (ranging from 1-4) with higher scores indicative of higher levels of exhaustion/disengagement/inattentiveness/burnout.
Moral stress at workBaseline (Day 1), One week, 1, 3, and 6 month follow-up5 self-report items measuring moral stress at work on a 4-point scale ranging from 1 (Strongly agree) to 4 (Strongly disagree). All items are summed. Potential scores range from 5-20, with higher scores indicative of lower levels of moral stress.
Adverse eventsOne week and 1, 3, and 6 month follow-upA free text response field measuring the occurrence of any health problems since the last contact.
Future self questionnaire - shortened version3 month follow-upA free text response field asking to imagine a future self identity. Then a free text response field to describe a mental image of this identity, 2 items measuring vividness (from 1 not vivid at all to 10 very vivid) and positivity (from 1 very negative to 10 very positive) of that image on a 10-point scale and 1 item measuring the perspective of viewing that mental image (through own eyes or as if seeing oneself) before and after the traumatic event(s). Higher scores on rating scales indicate higher levels of vividness/positivity.
Self-rated concentration disruption associated with intrusive memoriesBaseline (Day 1), Week 1 and Week 5, 1, 3, and 6 months follow-upTwo items measuring the level of concentration disruption associated with the intrusions (11 point scale from 0 to 10) and the duration of disruption (\< 1 min, 1-5 min, 5-10 min, 10-30 min, 30-60 min, \> 60 min). High scores indicate higher level of concentration disruption and longer duration of disruption.
Coping mechanismsBaseline (Day 1)2 free text response field questions (e.g. Are there any specific factors you think have made it easier for you to handle the COVID-19 situation and its consequences?) at Day 1.
WHODAS 2.06 month follow-up12 self-rated items assessing functioning in six life domains: 1) cognition, 2) mobility, 3) personal care 4) relations, 5) daily activities and 6) participation in society. Each item is rated on a 5-point scale, from 1 (none) to 5 (extreme or cannot do) and summed; a higher sum score indicates worse functioning. An additional three questions are asked at the end regarding the frequency and impact of these items.
Credibility/expectancy questionnaireDay 15 item questionnaire (11-point scale from 0 to 10) that rates to what degree the participant finds the intervention credible. High scores indicate greater credibility.
Subjective Units of Distress (SUDS)Day 1A bespoke manipulation check item measuring self-rated distress during the intervention/control procedure (11-point scale from 0 to 10) at 3 times during the intervention process. Higher scores indicate higher level of distress.
Feedback questionnaire about participation1 month follow-up8 bespoke items including questions about study participation e.g. how acceptable was it to do the task? Rated on 11-point scale from 0 (not at all) to 10 (extremely), higher scores indicate higher acceptability; and questions about what has happened since the study with a yes/no response e.g. have you had any psychological or medical treatment since you did the task; and items with a free text response field e.g. do you have any other comments.
Time perspective questionnaireBaseline (Day 1), One week, 1, 3, and 6 month follow-up8 self-report items (5-point scale from 1 to 5) measuring time perspective on three subscales: past perspective (items 3, 5, 7), present perspective (items 1, 8) and future perspective (items 2, 4, 6). Item scores for each subscale will be summed. Higher values indicate higher levels of past/present/future time perspective.
Concentration and memory difficulties6 month follow-upEleven items assess the extent of concentration and memory difficulties during the previous four weeks, using a 5-point scale (1 'Virtually every day' to 5 'Never'). Total scores range from 11 to 55; higher scores indicate less concentration and memory difficulties.
Self-rated functioning and social support ratingsBaseline (Day 1), One week, 1, 3, and 6 month follow up3 bespoke items including a question on impact on work-related functioning, and one on daily functioning in other areas associated with the intrusions and a question on perceived social support after the traumatic event. All items are rated on an 11-point scale (from 0 none; 5 some; 10 extreme/much). Higher scores indicate higher level of functional impairment/perceived social support.
Appraisals of intrusive memoriesBaseline (Day 1), One week, 1, 3, and 6 month follow-up6 self-report items (11-point scale from 0 to 100) measuring appraisals of intrusions on two subscales: psychological problems (items 1-3) and negative self-evaluations (items 4-6). Items for each subscale will be summed. Possible subscale scores range from 0 - 300, with higher values indicative of worse appraisals.
Self-rated sleep ratingsBaseline (Day 1), one week and 1, 3, and 6 month follow-upTwo self rated items: Item 1 measures the extent of being troubled by poor sleep (with reference to study event) on a 5 point scale (from not at all to very much), and item 2 measures the number of nights in the week with sleep problems on a 5 point scale (from 0-1 to 5-7 nights). Each 5-point scale is reverse scored (4 - 0) then summed. Possible total scores range from 0 - 8, with higher values indicative of better sleep.
Self Rated Health (SRH) ratingBaseline (Day 1), one week, and 1, 3, and 6 month follow-upA single item measuring perceived health status on a seven-point scale (from very good to very bad). The scale is reverse scored. High scores indicate good outcomes.
Questions related to work situationBaseline (Day 1), One week, 1, 3, and 6 month follow-up3 free text response field questions (e.g. which type of health care do you work with right now?) at Day 1 and two free text response field questions on whether the work situation changed and if yes, how, at one week, 1, 3, and 6 month follow-up.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026