Trial · NCT00958880
Yohimbine to Enhance Cognitive Behavioral Therapy (CBT) for Social Anxiety
NCT00958880, Phase 3, Completed, Southern Methodist University; results first posted 2013-11-11
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Yohimbine to Enhance Cognitive Behavioral Therapy (CBT) for Social Anxiety. Trials, record NCT00958880. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00958880
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Yohimbine to Enhance Cognitive Behavioral Therapy (CBT) for Social Anxiety
- NCT number
- NCT00958880
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 40 participants, actual
- Lead sponsor
- Southern Methodist University
- Conditions
- Social Anxiety Disorder
- Interventions
- Group Cognitive Behavioral Therapy, Yohimbine Hydrochloride, Sugar Pill
- First posted
- 2009-08-13
- Last updated
- 2013-11-11
- Results first posted
- 2013-11-11
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The Liebowitz Social Anxiety Scale (LSAS) | LSAS means at 1 month follow-up | The Liebowitz Social Anxiety Scale (LSAS) is a self-report measure of social anxiety symptom severity. Scores range from 0 to 144, with higher scores indicating more social anxiety symptoms severity (i.e., a worse outcome). |
| Secondary | Social Phobic Disorders Severity and Change Form | CGI change scores from baseline to 1 month follow-up | Social Phobic Disorders Severity and Change (SPDSC) Form is a version of the Clinical Global Improvement-Severity scale adapted specifically for clinician ratings of social anxiety disorder symptom severity. The scale ranges from 0 to 5, with higher scores indicating more social anxiety symptoms severity (i.e., worse outcomes). We examined the change in SPDSC scores from baseline to a 1 month follow-up. |
Source ClinicalTrials.gov
Outcomes2
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | The Liebowitz Social Anxiety Scale (LSAS) | LSAS means at 1 month follow-up | units on a scale | MEAN | |
| SECONDARY | Social Phobic Disorders Severity and Change Form | CGI change scores from baseline to 1 month follow-up | units on a scale | MEAN |
Source ClinicalTrials.gov
Results by group4
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| The Liebowitz Social Anxiety Scale (LSAS) | Sugar Pill | 41.0 | Standard Deviation 22.0 | units on a scale | |
| The Liebowitz Social Anxiety Scale (LSAS) | Yohimbine Hydrochloride | 33.3 | Standard Deviation 17.5 | units on a scale | |
| Social Phobic Disorders Severity and Change Form | Sugar Pill | 2.0 | Standard Deviation 0.9 | units on a scale | |
| Social Phobic Disorders Severity and Change Form | Yohimbine Hydrochloride | 2.0 | Standard Deviation 0.8 | units on a scale |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Sugar Pill | 20 | |
| Overall Study | STARTED | Yohimbine Hydrochloride | 20 | |
| Overall Study | COMPLETED | Sugar Pill | 18 | |
| Overall Study | COMPLETED | Yohimbine Hydrochloride | 18 | |
| Overall Study | NOT COMPLETED | Sugar Pill | 2 | |
| Overall Study | NOT COMPLETED | Yohimbine Hydrochloride | 2 |
Source ClinicalTrials.gov
Adverse events36
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Sweaty palms | General disorders | Sugar Pill | 1 | 20 | 1 |
| other | Sweaty palms | General disorders | Yohimbine Hydrochloride | 0 | 20 | 0 |
| other | Headache | General disorders | Sugar Pill | 3 | 20 | 3 |
| other | Headache | General disorders | Yohimbine Hydrochloride | 2 | 20 | 2 |
| other | Decrease in sexual arousal | General disorders | Sugar Pill | 1 | 20 | 1 |
| other | Decrease in sexual arousal | General disorders | Yohimbine Hydrochloride | 0 | 20 | 0 |
| other | Insomnia | General disorders | Sugar Pill | 0 | 20 | 0 |
| other | Insomnia | General disorders | Yohimbine Hydrochloride | 2 | 20 | 2 |
| other | Crying | General disorders | Sugar Pill | 0 | 20 | 0 |
| other | Crying | General disorders | Yohimbine Hydrochloride | 1 | 20 | 1 |
1 to 10 of 36Source ClinicalTrials.gov
See all 36 adverse eventsAdverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Sugar Pill | ||
| Total, all-cause mortality | Yohimbine Hydrochloride | ||
| Total, other adverse events | Sugar Pill | 5 | 20 |
| Total, other adverse events | Yohimbine Hydrochloride | 19 | 20 |
| Total, serious adverse events | Sugar Pill | 0 | 20 |
| Total, serious adverse events | Yohimbine Hydrochloride | 0 | 20 |
Source ClinicalTrials.gov
Papers2
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons1
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison |
|---|
| Sugar Pill vs Yohimbine Hydrochloride: serious adverse events |
Source Trial comparisons
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT00958880
GET https://conductscience.org/api/trials/v1/NCT00958880/events?page=2