- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03271437
Flash Open Trial With Therapists In Training
September 4, 2017 updated by: Trauma Institute & Child Trauma Institute
This study will test the eye movement desensitization and reprocessing (EMDR) based Flash technique and a progressive counting (PC) based variant.
EMDR-trained therapists will be trained in the standard Flash, and PC-trained therapists will be trained in PC Flash.
In each group they will try it with a minor upsetting memory, and then with two more significant upsetting memories.
Participants will use the subjective units of distress scale (SUDS) to rate distress pre- and post-treatment.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
200
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
-
-
Massachusetts
-
Northampton, Massachusetts, United States, 01060
- Recruiting
- Trauma Institute & Child Trauma Institute
-
-
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
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Therapist trained by Trauma Institute & Child Trauma Institute in EMDR or PC
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: TREATMENT
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: PC-trained therapists
|
Progressive counting with Flash technique
|
EXPERIMENTAL: EMDR-trained therapists
|
Eye movement desensitization and reprocessing with Flash technique
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in SUDS following treatment
Time Frame: Pre-treatment, immediately post-treatment, one week post-treatment, and one month post-treatment
|
Subjective units of distress scale
|
Pre-treatment, immediately post-treatment, one week post-treatment, and one month post-treatment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this 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 (ANTICIPATED)
September 15, 2017
Primary Completion (ANTICIPATED)
November 30, 2017
Study Completion (ANTICIPATED)
November 30, 2017
Study Registration Dates
First Submitted
August 31, 2017
First Submitted That Met QC Criteria
August 31, 2017
First Posted (ACTUAL)
September 5, 2017
Study Record Updates
Last Update Posted (ACTUAL)
September 7, 2017
Last Update Submitted That Met QC Criteria
September 4, 2017
Last Verified
September 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2017-1003
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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