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Clinical Trials/NCT03271398
NCT03271398
Unknown
Not Applicable

Intensive Therapy Archival Research

Trauma Institute & Child Trauma Institute1 site in 1 country1,200 target enrollmentAugust 2, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Trauma, Psychological
Sponsor
Trauma Institute & Child Trauma Institute
Enrollment
1200
Locations
1
Primary Endpoint
Change in TSI-2 following treatment
Last Updated
8 years ago

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.

Registry
clinicaltrials.gov
Start Date
August 2, 2017
End Date
December 31, 2022
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Trauma Institute & Child Trauma Institute
Responsible Party
Sponsor

Eligibility Criteria

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

Study Sites (1)

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