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Bilateral Brain Stimulation in Trauma Therapy

Bilateral Brain Stimulation in Trauma Therapy: a Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03086083
Enrollment
40
Registered
2017-03-22
Start date
2013-10-21
Completion date
2015-08-28
Last updated
2017-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Handling (Psychology), Intervention Study

Keywords

Traumatic memories, comparative study, single session, EMDR, Beck inventory

Brief summary

Comparatively studied the effects of Eye Movement Desensitization and Reprocessing (EMDR) bilateral brain stimulation in trauma therapy. A randomized, parallel, before-after, blind study was performed.

Detailed description

Comparatively studied the effects of Eye Movement Desensitization and Reprocessing (EMDR) bilateral brain stimulation in trauma therapy. A randomized, parallel, before-after, blind study was performed. Thirty nine subjects were randomly distributed to two groups: one session of EMDR psychotherapy standard and other with EMDR standard protocol without its typical brain bilateral stimulation. The results of the Beck scales for anxiety, depression and hopelessness and the impact of events test were compared between groups.

Interventions

BEHAVIORALEMDR standard protocol

Patient have only one standard EMDR session about a traumatic situation remembered by him.

BEHAVIORALprotocol without brain stimulation

Patient have only one standard EMDR session about a traumatic situation remembered by him, however, without the bilateral brain stimulation.

Sponsors

Sao Jose do Rio Preto Medical School
CollaboratorOTHER
Ciclo de Mutação
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

All participants was invited to one session of brief Psychotherapy with a new model. To the outcome assessor was said to study if was significant difference between those data from two groups α e β.

Intervention model description

A randomized, parallel, before-after, blind study was performed. Thirty nine subjects were randomly distributed to two groups: one session of EMDR psychotherapy standard and other with EMDR standard protocol without its typical brain bilateral stimulation. The results of the Beck scales for anxiety, depression and hopelessness and the impact of events test were compared between groups.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Inclusion criteria for the study were to be a university student, over 18 years old, to have a complaint associated to a traumatic life event and to have accepted to participate of the study.

Exclusion criteria

*

Design outcomes

Primary

MeasureTime frameDescription
Impact of Events TestBefore and immediately after the psychotherapy session, which has average of 1:30 hours.Self-administered questionnaire to measure Impact of the traumatic event, which the patient have selected for this intervention
Beck scale for anxietyBefore and immediately after the psychotherapy session, which has average of 1:30 hours.Self-administered questionnaire to measure anxiety, in this case, when the patient are thinking about that specific traumatic event, which he or she selected for this intervention.

Secondary

MeasureTime frameDescription
Change from baseline Beck scale for depression at the final of sessionBefore and immediately after the conclusion of the session, which has average of 1:30 hoursSelf-administered questionnaire to measure depression, in this case, when the patient are thinking about that specific traumatic event, which he or she select for this intervention.
Change from baseline Beck scale for hopelessness at the final of sessionBefore and immediately after the conclusion of the session, which has average of 1:30 hoursSelf-administered questionnaire to measure hopelessness

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026