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Clinical Trials/NCT03271398
NCT03271398UnknownNot Applicable

Intensive Therapy Archival Research

Trauma Institute & Child Trauma Institute1 site in 1 country1,200 target enrollmentStarted: August 2, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
1,200
Locations
1
Primary Endpoint
Change in TSI-2 following treatment

Study Overview

Brief Summary

This is an internal treatment evaluation to determine whether eye movement desensitization and reprocessing (EMDR) or progressive counting (PC) should become the preferred trauma treatment for the investigator's clients. The investigator is using routine/existing in-house measures and case files to track symptom reduction, trauma treatment time, rate of treatment switching (from EMDR to PC or vice versa), and rate of trauma treatment refusal. This is retrospective as well as prospective archival research.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Other

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Victims of crimes, including assault, rape, robbery, intimate partner violence, child abuse, kidnapping, vehicular homicide, and suicide
  • Witnesses and family members of victims

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in TSI-2 following treatment

Time Frame: Administered pre-treatment, two weeks post-treatment, and 12 weeks post-treatment

Trauma Symptom Inventory-2

Change in TSCC following treatment

Time Frame: Administered pre-treatment, two weeks post-treatment, and 12 weeks post-treatment

Trauma Symptom Checklist for Children

Change in PRS following treatment

Time Frame: Administered pre-treatment, two weeks post-treatment, and 12 weeks post-treatment

Problem Rating Scale

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Trauma Institute & Child Trauma Institute
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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