- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03760601
A Brief Cognitive Intervention After Intrusive Memories of Trauma With Young Refugees: An Extension
August 31, 2022 updated by: Emily Holmes, Karolinska Institutet
Intrusive Memories of Trauma Experienced by Young Refugees: Using Single Case Experimental Design to Investigate a Brief Cognitive Intervention Involving Computer Gameplay: An Extension
This research study is designed to investigate the use of a simple cognitive task (a memory cue and 10 minute time gap, followed by playing the computer game "Tetris") for decreasing the number of intrusive memories of trauma among young refugees and asylum seekers.
The design is a single case experimental AB design with optional replication (ABAB).
Participants will aim to complete a no-intervention phase ('A': baseline phase) of one week followed by a one-week intervention phase ('B'), including a one-session intervention with a researcher comprising the simple cognitive task, followed by instructions to continue to use the technique self-guided in the subsequent week.
Follow ups are conducted after each week to monitor the occurrence of intrusive memories of trauma in a pen-and-paper diary.
It is predicted that participants will report fewer intrusive memories during the intervention phase than during the preceding baseline phase.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
This research study follows from ClinicalTrials.gov
ID: NCT03525158, with a focus on the ABAB design and adding additional questions e.g. on concentration, emotion and functioning, and with the possibility of focusing on 1 intrusive memory at a time with associated distress ratings as part of the procedure.
Study Type
Interventional
Enrollment (Actual)
5
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Stockholm, Sweden
- Swedish Language Classes for Refugees, Clinics
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 100 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Refugee or asylum seeker
- Experiencing intrusive memories of trauma
- Have access to a smartphone
- Able to speak or read the study material in Swedish, English, Arabic or Farsi
- Able to attend five to six meetings with a researcher
Exclusion Criteria:
- Exhibit psychotic symptoms or other symptoms of severe mental illness
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: NON_RANDOMIZED
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
NO_INTERVENTION: Baseline phase ('A')
Measurements collected in a pen-and-paper diary four times a day (morning, afternoon, evening and night) over one week for the primary outcome (occurrence of intrusive memories of trauma).
Individual baseline phases will be used as control periods.
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EXPERIMENTAL: Intervention phase ('B')
A one-session intervention with a researcher including a simple cognitive task (a memory cue, 10 minutes time gap and ca.
20 minutes of Tetris game-play) followed by instructions to engage in the task selfguided over the subsequent week.
Measurements collected in a pen-and-paper diary four times a day over one week following the intervention for the primary outcome (occurrence of intrusive memories of trauma).
|
A one-session intervention with a researcher including a simple cognitive task (a memory cue, 10 minutes time gap and ca.
20 minutes of Tetris game play) with instructions to engage in the task self-guided in the subsequent week.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in number of intrusive memories of trauma
Time Frame: Change between baseline week 1 and Intervention week 1
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Number of intrusive memories of traumatic event recorded by participants in a diary daily (morning, afternoon, evening and night) over one week.
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Change between baseline week 1 and Intervention week 1
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility and acceptability ratings for using a smartphone game-play intervention
Time Frame: Intervention week 1
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Feasibility and Acceptability of the intervention assessed with 10 self-rated items, e.g.
"Would you recommend playing Tetris to a friend?".
Scores range from 0 - 10 with higher scores indicating greater acceptability/ feasibility.
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Intervention week 1
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Feasibility and acceptability - open ended questions
Time Frame: Intervention week 1
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Two items with open-ended follow-up questions: "How did you feel about playing Tetris after you had an intrusive memory?" and "Why"?
or "How much would you prefer an intervention that is delivered by a computer/ smartphone compared to seeing a doctor/psychologist in person?" and "Why"?
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Intervention week 1
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Self-guided intervention adherence - usage of the gameplay intervention in daily life
Time Frame: Intervention week 1
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Usage of the gameplay intervention assessed with 4 self-rated items: 1. Did you play Tetris in the last week since the last meeting?
(Yes/No).
2. If yes, how many days did you play Tetris in the last week since we first practiced the game together?
3. How long did you spend playing Tetris at a time?
(<10 min - >30 min), 4. How often did you manage to play Tetris after you experienced an intrusive memory?
(11-point scale; 0 = not at all; 10 = every time).
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Intervention week 1
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Impact of intrusive memories on concentration, control, sleep and stress - ratings
Time Frame: Baseline week 1 and Intervention week 1
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A bespoke measure of 6 self-rated items to assess the impact of intrusive memories on concentration, control, sleep and stress (all rated on an 11-point scale): 2 items assessing experienced concentration difficulties due to intrusive memories and in general ( high scores indicating more concentration difficulties);1 item assessing feeling of control over intrusive memories (0 = no control; 10 = in full control); 2 items assessing sleep disturbances due to intrusive memories (higher scores indicating more sleep disturbance); and 1 item assessing to what degree intrusive memories affected stress levels (0 = not at all; 10 = affected very much).
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Baseline week 1 and Intervention week 1
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Rating of how long intrusive memories disrupted concentration on average
Time Frame: Baseline week 1 and Intervention week 1
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1 item assessing for how long intrusive memories disrupted concentration on average (<1 minute - > 60 minutes)
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Baseline week 1 and Intervention week 1
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Impact of intrusive memories - open ended questions
Time Frame: Baseline week 1 and Intervention week 1
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Two open-ended questions are included: "How do intrusive memories interfere with your concentration?" and "How do intrusive memories interfere with your ability to settle in to this country and learn new skills, e.g. a new language?"
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Baseline week 1 and Intervention week 1
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Impact of the intervention on concentration, emotion and functioning - ratings
Time Frame: Intervention week 1
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A bespoke measure comprising 3 self-rated items to assess the impact of the intervention on concentration, emotion and functioning at the time of playing (11-point scale, 0= not helpful, 10= very helpful).
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Intervention week 1
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Subjective impact of the intervention - open ended questions
Time Frame: Intervention week 1
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2 open ended questions about the subjective impact of the intervention in the shorter, and longer term: "How would you describe the impact of this intervention in the short term?"; "How would you describe the impact of this intervention in the longer term"?
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Intervention week 1
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World Health Organization Disability Assessment Schedule 2.0 (WHODAS)
Time Frame: Baseline week 1 and intervention week 1
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A 12 item self-rated questionnaire asking about difficulties due to health conditions, including mental or emotional problems.
Scores range from 1 to 5 where 1=none and 5=extreme or cannot do.
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Baseline week 1 and intervention week 1
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
March 25, 2019
Primary Completion (ACTUAL)
June 20, 2019
Study Completion (ACTUAL)
August 26, 2019
Study Registration Dates
First Submitted
November 19, 2018
First Submitted That Met QC Criteria
November 29, 2018
First Posted (ACTUAL)
November 30, 2018
Study Record Updates
Last Update Posted (ACTUAL)
September 2, 2022
Last Update Submitted That Met QC Criteria
August 31, 2022
Last Verified
August 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2018/2149-32
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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