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Facilitation of Fear Extinction With Yohimbine Hydrochloride in Phobic Participants

Facilitation of Fear Extinction With Yohimbine Hydrochloride in Phobic Participants

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00734422
Enrollment
67
Registered
2008-08-14
Start date
2008-07-31
Completion date
2010-07-31
Last updated
2018-09-13

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

Conditions

Phobic Disorders

Keywords

Phobic Disorders (Fear of Flying), Virtual Reality Exposure Therapy, Fear extinction, Yohimbine

Brief summary

Procedurally Virtual reality exposure therapy (VRET) is quite similar to models of extinction of conditioned fears. Recent advances in animal research have identified pharmacological agents that appear to both accelerate and consolidate extinction learning. One of these cognitive enhancers is Yohimbine. An interesting finding in animal literature is that the administration of Yohimbine during extinction trials accelerates fear reduction and may convert ineffective exposures in to successful ones. It is thought that the mechanism of enhanced emotional memory is through elevated norepinephrine in the prefrontal cortex. Therefore, we propose to extend these studies by combining VRET with Yohimbine. In this pilot study with a between groups design 20 participants with a fear of flying will be treated with VRET plus Yohimbine or VRET plus placebo. This between groups design was chosen to further characterize the differential within and between trial extinction. Outcome will be measured by self-report, behavioral, and psychophysiological assessments at pre- and post-treatment. In addition, we will examine extinction parameters during exposures.

Interventions

BEHAVIORALVirtual Reality Exposure Therapy

Standard virtual reality exposure therapy for fear of flying will be combined with the administration of either yohimbine hydrochloride or an inactive placebo pill.

Sponsors

VU University of Amsterdam
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* DSM-IV diagnosis of specific phobia (fear of flying). * Between the ages of 18-65 * Sufficient fluency in Dutch to complete treatment and research protocol

Exclusion criteria

* Presence of medical condition, assessed by self-report questionnaires at the intake (i.e., pregnancy, seizure disorder, respiratory disorder, cardiovascular disease, pacemaker, hypertension). * Resting blood pressure higher than 140 (systolic) or 105 (diastolic) * Unstable psychotropic medication. * Current use of tranquilizers (Benzodiazepines) * Psychosis * Depression with suicidal ideation * Dementia or other severe cognitive impairment * Substance dependence * Bipolar disorder * Borderline personality disorder * Anti-social personality disorder * Current use of beta-blockers

Design outcomes

Primary

MeasureTime frame
Flight Anxiety Situations Questionnaire (self-report); Flight Anxiety Modality Questionnaire (self-report)Assessed at pre- and post-treatment and 9-12 months follow-up

Secondary

MeasureTime frame
Severity of Anxiety Symptoms (Beck Anxiety Inventory) Anxiety Sensitivity (Anxiety Sensitivity Inventory)Assessed at pre- and post-treatment and 9-12 months follow-up

Countries

Netherlands

Outcome results

None listed

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