NCT05171868

Brief Summary

Objectives:

  1. 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. 2.To test whether reducing stress and psychological trauma reduces suicidal ideation in police officers.
  3. 3.To explore participants' experiences with EMDR Intervention.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
18 days until next milestone

First Posted

Study publicly available on registry

December 29, 2021

Completed
5 months until next milestone

Study Start

First participant enrolled

May 20, 2022

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2024

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2025

Completed
Last Updated

May 17, 2024

Status Verified

May 1, 2024

Enrollment Period

2.6 years

First QC Date

December 11, 2021

Last Update Submit

May 16, 2024

Conditions

Keywords

Forensic settingsEMDRTraumaPolice PersonnelSuicidal IdeationStressPakistanFeasibility

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

EXPERIMENTAL

EMDR 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.

Behavioral: Eye Movement Desensitization and Reprocessing (EMDR)

Waiting list Control Group

NO INTERVENTION

The 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.

EMDR receiving group

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

RECRUITING

MeSH Terms

Conditions

Suicidal IdeationPsychological TraumaWounds and Injuries

Interventions

Eye Movement Desensitization Reprocessing

Condition Hierarchy (Ancestors)

SuicideSelf-Injurious BehaviorBehavioral SymptomsBehaviorStress Disorders, TraumaticTrauma and Stressor Related DisordersMental Disorders

Intervention Hierarchy (Ancestors)

Desensitization, PsychologicBehavior TherapyPsychotherapyBehavioral Disciplines and Activities

Study Officials

  • Nusrat Husain

    University of Manchester

    PRINCIPAL INVESTIGATOR
  • Nasim Chahudhry

    Pakistan Institute of Living and Learning

    PRINCIPAL INVESTIGATOR

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

Locations