Eye Movement Desensitization and Reprocessing (EMDR) for Police Personnel
1 other identifier
interventional
80
1 country
1
Brief Summary
Objectives:
- 1.To examine the feasibility of Eye Movement Desensitization and Reprocessing (EMDR) as an intervention to reduce psychological trauma and stress amongst police officers in Pakistan.
- 2.To test whether reducing stress and psychological trauma reduces suicidal ideation in police officers.
- 3.To explore participants' experiences with EMDR Intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2022
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 11, 2021
CompletedFirst Posted
Study publicly available on registry
December 29, 2021
CompletedStudy Start
First participant enrolled
May 20, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2025
CompletedMay 17, 2024
May 1, 2024
2.6 years
December 11, 2021
May 16, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Feasibility of recruitment
The feasibility will be determined by collecting data on recruitment rates. The success criterion of feasibility will be to recruit \> 50% of eligible participants.
From baseline to 8th week (at the end of intervention)
Acceptability measure
Intervention acceptability will be assessed using data on intervention attendance. The criterion for acceptability is the intervention attendance rate of \> 5 sessions.
From baseline to 8th week (at the end of intervention)
Feasibility of Retention
The feasibility of retention will be determined by collecting data on retention rates. The success criterion of feasibility of retention will be to retain \> 50% participants.
From baseline to 8th week (at the end of intervention)
Secondary Outcomes (6)
Beck Scale for Suicide Ideation
Change in problem scores from baseline to 8th week
The International Trauma Questionnaire
Change in problem scores from baseline to 8th week
Depression Anxiety and Stress Scale
Change in problem scores from baseline to 8th week
Beck Hopelessness Scale
Change in problem scores from baseline to 8th week
Sleep Quality Questionnaire
Change in problem scores from baseline to 8th week
- +1 more secondary outcomes
Study Arms (2)
EMDR receiving group
EXPERIMENTALEMDR is a psychotherapeutic approach that emphasizes the role of the brain's information processing system in perfecting the psychological consequences of distressing events. EMDR is an eight-phase treatment protocol, including procedure that focuses on the memories underlying current problems and those that must be specifically addressed to bring the client to a robust state of psychological health. One of its distinguishing aspects is its use of bilateral physical stimulation, such as side-to-side eye movements, alternating hand taps, or alternating auditory tones while the person undergoing treatment is mentally focusing on aspects of various life experiences.
Waiting list Control Group
NO INTERVENTIONThe control group will receive their routine care as usual. Once the trial is completed they will be invited for EMDR sessions
Interventions
Each participant in the intervention group will receive 8 individual, weekly EMDR sessions over 8 weeks. Each session will take approximately 60-90 minutes. The sessions will be delivered at a place convenient to the participant. Trained EMDR therapists will deliver the intervention.
Eligibility Criteria
You may qualify if:
- Having suicidal ideation measured as a score \> 2 on Beck scale of suicidal ideation
- Aged 18 years - 60 years' old
- Police officer with psychological trauma measured with the International Trauma Questionnaire and stress measured with stress subscale of Depression, Anxiety and Stress scale
You may not qualify if:
- Less than 12 months' experience in the police officer.
- Participants reporting active suicidal ideation measured as a score of 2 on item no 4 of BSSI will be excluded and referred to a psychiatric service.
- With current history of use of hard/psychoactive substances (excluding tobacco and caffeine).
- Unable to provide consent due to severe mental or physical illness.
- Unlikely to be available for the entire duration of the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Prison settings Peshawar
Peshawar, KPK, 25000, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Nusrat Husain
University of Manchester
- PRINCIPAL INVESTIGATOR
Nasim Chahudhry
Pakistan Institute of Living and Learning
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 11, 2021
First Posted
December 29, 2021
Study Start
May 20, 2022
Primary Completion
December 30, 2024
Study Completion
June 30, 2025
Last Updated
May 17, 2024
Record last verified: 2024-05
Data Sharing
- IPD Sharing
- Will not share