Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
160 participants
INTERVENTIONAL
2015-12-31
2017-05-07
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Mismatch vs. Standard Intervention During Memory Reconsolidation Blockade With Propranolol: Effect on Psychophysiological Reactivity During Traumatic Imagery
NCT05853627
EMDR Treatment in PTSD Following Cardiac Events
NCT04672551
Evaluation of Desensitization Therapy and Re-treatment of Eye Movement Information [EMDR] in Patients With Post-traumatic Stress Disorder [PTSD]
NCT04431765
Eye-Movement Desensitization and Reprocessing in the ED and Post-Traumatic Syndrome
NCT03194386
Developing Memory Reconsolidation Blockers as Novel Posttraumatic Stress Disorder (PTSD) Treatments
NCT01490697
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
BASIC_SCIENCE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Delayed Bilateral Eye Movements
Delayed Bilateral Eye Movements after reactivation of fear-memory.
Delayed Bilateral Eye Movements
Bilateral Eye Movements followed by a 10 min delay after reactivation of fear-memory.
Undelayed Bilateral Eye Movements
Undelayed Bilateral Eye Movements after reactivation of fear-memory.
Undelayed Bilateral Eye Movement
Bilateral Eye Movements followed by no delay after reactivation of fear-memory. reactivation of the fear memory trace during which the reactivated memory is assumed to be in a labile state.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Delayed Bilateral Eye Movements
Bilateral Eye Movements followed by a 10 min delay after reactivation of fear-memory.
Undelayed Bilateral Eye Movement
Bilateral Eye Movements followed by no delay after reactivation of fear-memory. reactivation of the fear memory trace during which the reactivated memory is assumed to be in a labile state.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Presence of a manageable, nonphobic fear of spiders as determined by scores above the mean (male: 8.06; female: 10.46) on the German adapted Spider Phobia Questionnaire (SPQ; 38) and phobia criteria extracted from the Structured Clinical Interview for DSM-5 Axis I Disorders (SCID-I; 39)
* Signed Informed Consent after being informed
Exclusion Criteria
* Current use of any medication (except contraceptives, herbal medicine)
* Known or suspected non-compliance, drug or alcohol misuse
* Presence of any current psychiatric disorders determined by the Mini International Neuropsychiatric Interview (MINI; 40)
* Inability to follow the procedures of the study, e.g. due to language problems
* No SC response to physical (Valsalva maneuver), psychological (mental arithmetic) and/or auditive (handclapping) stressor
18 Years
60 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Massachusetts General Hospital
OTHER
Harvard Medical School (HMS and HSDM)
OTHER
University of Zurich
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Christoph Müller-Pfeiffer
PD. Dr.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Christoph Mueller-Pfeiffer, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital of Zurich, Department of Psychiatry and Psychotherapy
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University Hospital Zurich, Department of Psychiatry and Psychotherapy
Zurich, Canton of Zurich, Switzerland
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
F-86401-09-01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.