A Single-Component CBT for GAD
Behavioural Experiments for Intolerance of Uncertainty: A Single-Component Treatment for Generalized Anxiety Disorder
1 other identifier
interventional
60
1 country
1
Brief Summary
Generalized Anxiety Disorder (GAD) is a chronic condition that is characterized by excessive and uncontrollable worry and anxiety. In Canada, 3 to 4% of the population suffer from GAD at any point in time. These individuals have a lowered quality of life and are at risk for many medical conditions such as coronary heart disease and cancer. Research suggests that both pharmacological and psychological approaches are effective for treating GAD in the short-term; however, psychological treatments appear to offer the greatest long-term benefits. There exist a number of effective psychological treatments for GAD, most of which fall into the category of cognitive-behavioural therapy or CBT. In the 1990s, a group of Canadian investigators developed a CBT protocol for GAD that included four components. Data from five clinical trials suggest that one of the four components is particularly important for treatment success: experiencing uncertainty rather than avoiding it in everyday life. Stated differently, learning to tolerate and deal with uncertainty appears to be the key to decreasing worry and anxiety. Given this finding, the investigators have developed a new treatment that exclusively targets intolerance of uncertainty: Behavioural Experiments for Intolerance of Uncertainty or BE-IU. The goal of the current proposal is to test the efficacy of BE-IU by comparing it to a Waiting List (WL) control condition. A total of 50 participants with a primary diagnosis of GAD will be randomly assigned to either BE-IU or WL and will be assessed at 5 time points ranging from pre-treatment to 12-month follow-up. The conditions will be compared in terms of treatment efficacy and mechanisms. The investigators will also examine the predictors of change during the 12-months following treatment. The proposed study will produce data on the efficacy and mechanisms of a treatment for GAD that is less costly, less complex and easier to disseminate than treatments that are currently available.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2015
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 15, 2015
CompletedFirst Posted
Study publicly available on registry
September 16, 2015
CompletedStudy Start
First participant enrolled
October 1, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2018
CompletedJune 5, 2020
June 1, 2020
3 years
September 15, 2015
June 4, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Clinician's Severity Rating (CSR) of Anxiety Disorders Interview Schedule (ADIS)
Structured diagnostic interview
12 weeks
Secondary Outcomes (4)
Penn State Worry Questionnaire (PSWQ)
12 weeks
Worry and Anxiety Questionnaire (WAQ)
12 weeks
Beck Anxiety Inventory (BAI)
12 weeks
Beck Depression Inventory-II (BDI-II)
14 weeks
Other Outcomes (6)
Intolerance of Uncertainty Scale (IUS)
14 weeks
Safety Behaviours Questionnaire (SBQ)
14 weeks
Heart rate variability (HRV)
14 weeks
- +3 more other outcomes
Study Arms (2)
Behavioural experiments (CBT)
EXPERIMENTALBehavioural experiments involve selecting a specific thought to be tested (e.g., "uncertainty makes me unable to act") and designing a detailed experiment to test out the thought.
Waiting list
NO INTERVENTION12 week wait (with assessments) before being transferred to the experimental condition.
Interventions
Eligibility Criteria
You may qualify if:
- \) at least 18 years of age; 2) principal diagnosis of GAD; 3) no change in medication type or dose in 4 to 12 weeks before study entry (4 weeks for benzodiazepines, 12 weeks for antidepressants and hypnotics); 4) willingness to keep medication status stable while participating in the study; 5) no use of herbal products known to have CNS effects in the 2 weeks before study entry; 6) no evidence of suicidal intent (based on clinical judgement); 7) no evidence of current substance abuse, current or past schizophrenia, bipolar disorder or organic mental disorder; 8) no current participation in other trials; 9) no concurrent psychotherapy during treatment phase of trial; 10) no evidence of anxiety symptoms due to a general medical condition based on clinical judgement (e.g., clinical hyperthyroidism, hypoglycaemia, anaemia).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Universite du Quebec en Outaouaislead
- Canadian Institutes of Health Research (CIHR)collaborator
- Concordia University, Montrealcollaborator
- University College, Londoncollaborator
Study Sites (1)
Université du Québec en Outaouais
Gatineau, Quebec, J8X 3X7, Canada
Related Publications (1)
Dugas MJ, Sexton KA, Hebert EA, Bouchard S, Gouin JP, Shafran R. Behavioral Experiments for Intolerance of Uncertainty: A Randomized Clinical Trial for Adults With Generalized Anxiety Disorder. Behav Ther. 2022 Nov;53(6):1147-1160. doi: 10.1016/j.beth.2022.05.003. Epub 2022 May 27.
PMID: 36229113DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Michel J Dugas, Ph.D.
Université du Québec en Outaouais
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Psychology
Study Record Dates
First Submitted
September 15, 2015
First Posted
September 16, 2015
Study Start
October 1, 2015
Primary Completion
October 1, 2018
Study Completion
October 1, 2018
Last Updated
June 5, 2020
Record last verified: 2020-06