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Clinical Trial of Transdiagnostic Cognitive-Behavior Therapy for Anxiety Disorders (T-CBT)

Primary Purpose

Panic Disorder, Agoraphobia, Social Anxiety Disorder

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Transdiagnostic Cognitive-Behavioral Therapy
Sponsored by
Université de Sherbrooke
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Panic Disorder focused on measuring Panic Disorder, Agoraphobia, Social Anxiety Disorder, Generalized Anxiety Disorder, Cognitive-Behavioral Therapy

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Aged 18-65 (upper age limit added 2016-11-18)
  • Fluent in spoken and written French.
  • Meeting DSM-5 diagnostic criteria for at least one of the following anxiety disorders as a primary mental disorder: Panic Disorder, Agoraphobia, Generalized Anxiety Disorder and/or Social Anxiety Disorder according to a clinical rating ≥ 4 for the Anxiety Disorders Interview Schedule for DSM-5 (ADIS-5) administered by a trained PhD-level clinician.

Exclusion Criteria:

  • Active suicidal intentions, psychosis, bipolar disorder, active substance-related disorder and addictive disorder in the past 12 months (sections or screening questions in ADIS-5).
  • Marked cognitive impairment [Épreuve des 5 mots (Dubois, 2002) administered in case of doubt by assessor].
  • Consultation with a psychiatrist in the past 12 months.

Sites / Locations

  • Centre intégré de santé et de services sociaux de Laval
  • Centre intégré universitaire de santé et de services sociaux de l'Estrie
  • Centre intégré universitaire de santé et de services sociaux de la Capitale-Nationale

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Transdiagnostic CBT

Treatment-as-usual

Arm Description

Group psychotherapy according to the Transdiagnostic Cognitive-Behavioral Therapy treatment protocol (Norton, 2012)

Treatment-as-usual and a differed intervention (if desired by participants) after the 8-month follow up.

Outcomes

Primary Outcome Measures

Change in Beck Anxiety Inventory (BAI)
Change in Clinical Severity Rating from the Anxiety Disorders Interview Schedule for DSM-5 - Adult Version (ADIS-5)

Secondary Outcome Measures

Change in Beck Anxiety Inventory (BAI)
Change in Clinical Severity Rating from the Anxiety Disorders Interview Schedule for DSM-5 - Adult Version (ADIS-5)
Change in Panic Disorder Severity Scale (Self-Report)
Change in Mobility Inventory for Agoraphobia
Change in Penn State Worry Questionnaire
Change in Social Phobia Inventory
Change in Patient Health Questionnaire (PHQ-9)
Change in EuroQol (EQ-5D-5L)
Change in Administrative databases records
Beneficiary registry (sex, birthdate, and death registry), Med-Écho hospitalizations (diagnosis, procedures), medical services (physician, diagnosis, acts, services) and pharmaceutical services (medication, dose, duration).
Change in Anxiety Disorder Diagnostic Questionnaire - weekly version (ADDQ-W)

Full Information

First Posted
May 24, 2016
Last Updated
September 13, 2019
Sponsor
Université de Sherbrooke
Collaborators
Canadian Institutes of Health Research (CIHR), Estrie University Integrated Health and Social Services Center - University Hospital of Sherbrooke, CISSS de Laval, Integrated University Health and Social Services Center of the Capitale-Nationale
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1. Study Identification

Unique Protocol Identification Number
NCT02811458
Brief Title
Clinical Trial of Transdiagnostic Cognitive-Behavior Therapy for Anxiety Disorders
Acronym
T-CBT
Official Title
A Pragmatic Randomized Controlled Trial of Group Transdiagnostic Cognitive-Behavior Therapy for Anxiety Disorders in Primary Care
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
September 12, 2016 (Actual)
Primary Completion Date
June 15, 2018 (Actual)
Study Completion Date
July 10, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Université de Sherbrooke
Collaborators
Canadian Institutes of Health Research (CIHR), Estrie University Integrated Health and Social Services Center - University Hospital of Sherbrooke, CISSS de Laval, Integrated University Health and Social Services Center of the Capitale-Nationale

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Anxiety disorders are the most common mental disorders in community settings, and they are associated with significant psychological distress, functional and social impairment. Although pharmacological and psychological treatments for anxiety and depression have existed for several years now, only a minority of anxiety disorder sufferers are treated according to guidelines. Cognitive behavior therapy (CBT) is the most consistently efficacious psychological treatment for anxiety disorders, but implementation of CBT in primary care is challenging due to limited resources. Recent studies indicate that transdiagnostic group CBT for multiple anxiety disorders could be a promising alternative to individual CBT in primary care. The aim of the study is to examine the effectiveness of group CBT for anxiety disorders as a complement to usual care. The clinical trial will be conducted in three Health and Social Services Centers in the province of Québec (i.e. Sherbrooke, Laval and Québec). Patients will be French-speaking adults with anxiety disorders, and they will be randomly assigned to one of two treatment conditions: a) Transdiagnostic group CBT (12 weekly 2-hour sessions), b) usual care. The transdiagnostic group CBT will be offered as a differed intervention to participants in the usual care group after the 8-month follow up. Participants in both study arms will undergo a baseline clinical evaluation as well as outcome assessment interviews at post-treatment, 4, 8, and 12 month follow-up time-points. The primary study results will include improvement on a questionnaire on anxiety symptoms. Widespread implementation of group CBT could lead to better outcomes for a large number of patients living with anxiety.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Panic Disorder, Agoraphobia, Social Anxiety Disorder, Generalized Anxiety Disorder
Keywords
Panic Disorder, Agoraphobia, Social Anxiety Disorder, Generalized Anxiety Disorder, Cognitive-Behavioral Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
231 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Transdiagnostic CBT
Arm Type
Experimental
Arm Description
Group psychotherapy according to the Transdiagnostic Cognitive-Behavioral Therapy treatment protocol (Norton, 2012)
Arm Title
Treatment-as-usual
Arm Type
No Intervention
Arm Description
Treatment-as-usual and a differed intervention (if desired by participants) after the 8-month follow up.
Intervention Type
Behavioral
Intervention Name(s)
Transdiagnostic Cognitive-Behavioral Therapy
Intervention Description
Treatment in the Transdiagnostic CBT condition will consist of 12 weekly 2-hour sessions following the manualized treatment protocol including psychoeducation, cognitive restructuring, exposure and relapse prevention.
Primary Outcome Measure Information:
Title
Change in Beck Anxiety Inventory (BAI)
Time Frame
Baseline and post-treatment; within two weeks after the 12th treatment session, based on the timeframe of the intervention group (treatment completion)
Title
Change in Clinical Severity Rating from the Anxiety Disorders Interview Schedule for DSM-5 - Adult Version (ADIS-5)
Time Frame
Baseline and post-treatment; within two weeks after the 12th treatment session, based on the timeframe of the intervention group (treatment completion) (Outcome 2 added 2017-12-12)
Secondary Outcome Measure Information:
Title
Change in Beck Anxiety Inventory (BAI)
Time Frame
Baseline, post-treatment, 4-month, 8-month and 12-month follow-ups
Title
Change in Clinical Severity Rating from the Anxiety Disorders Interview Schedule for DSM-5 - Adult Version (ADIS-5)
Time Frame
Baseline, post-treatment and 8-month follow-ups
Title
Change in Panic Disorder Severity Scale (Self-Report)
Time Frame
Baseline, post-treatment, 4-month, 8-month and 12-month follow-ups
Title
Change in Mobility Inventory for Agoraphobia
Time Frame
Baseline, post-treatment, 4-month, 8-month and 12-month follow-ups
Title
Change in Penn State Worry Questionnaire
Time Frame
Baseline, post-treatment, 4-month, 8-month and 12-month follow-ups
Title
Change in Social Phobia Inventory
Time Frame
Baseline, post-treatment, 4-month, 8-month and 12-month follow-ups
Title
Change in Patient Health Questionnaire (PHQ-9)
Time Frame
Baseline, post-treatment, 4-month, 8-month and 12-month follow-ups
Title
Change in EuroQol (EQ-5D-5L)
Time Frame
Baseline, post-treatment, 4-month, 8-month and 12-month follow-ups
Title
Change in Administrative databases records
Description
Beneficiary registry (sex, birthdate, and death registry), Med-Écho hospitalizations (diagnosis, procedures), medical services (physician, diagnosis, acts, services) and pharmaceutical services (medication, dose, duration).
Time Frame
Starting 12 months prior to participant enrollment up to the 12-month follow-up
Title
Change in Anxiety Disorder Diagnostic Questionnaire - weekly version (ADDQ-W)
Time Frame
ADDQ-W administered weekly over the course of the 12 weekly group therapy sessions to assess change in anxiety severity.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 18-65 (upper age limit added 2016-11-18) Fluent in spoken and written French. Meeting DSM-5 diagnostic criteria for at least one of the following anxiety disorders as a primary mental disorder: Panic Disorder, Agoraphobia, Generalized Anxiety Disorder and/or Social Anxiety Disorder according to a clinical rating ≥ 4 for the Anxiety Disorders Interview Schedule for DSM-5 (ADIS-5) administered by a trained PhD-level clinician. Exclusion Criteria: Active suicidal intentions, psychosis, bipolar disorder, active substance-related disorder and addictive disorder in the past 12 months (sections or screening questions in ADIS-5). Marked cognitive impairment [Épreuve des 5 mots (Dubois, 2002) administered in case of doubt by assessor]. Consultation with a psychiatrist in the past 12 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pasquale Roberge, Ph.D.
Organizational Affiliation
Université de Sherbrooke
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Martin D. Provencher, Ph.D.
Organizational Affiliation
Laval University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre intégré de santé et de services sociaux de Laval
City
Laval
State/Province
Quebec
ZIP/Postal Code
H7M3L9
Country
Canada
Facility Name
Centre intégré universitaire de santé et de services sociaux de l'Estrie
City
Sherbrooke
State/Province
Quebec
ZIP/Postal Code
J1G1B1
Country
Canada
Facility Name
Centre intégré universitaire de santé et de services sociaux de la Capitale-Nationale
City
Quebec
ZIP/Postal Code
G1C3S2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30285672
Citation
Roberge P, Provencher MD, Gosselin P, Vasiliadis HM, Gaboury I, Benoit A, Antony MM, Chaillet N, Houle J, Hudon C, Norton PJ. A pragmatic randomized controlled trial of group transdiagnostic cognitive-behaviour therapy for anxiety disorders in primary care: study protocol. BMC Psychiatry. 2018 Oct 3;18(1):320. doi: 10.1186/s12888-018-1898-1.
Results Reference
background
Links:
URL
https://bmcpsychiatry.biomedcentral.com/articles/10.1186/s12888-018-1898-1
Description
BMC Psychiatry

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Clinical Trial of Transdiagnostic Cognitive-Behavior Therapy for Anxiety Disorders

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