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Evaluation of a Cognitive Therapy (Inference-based-therapy) for the Treatment of Obsessional Compulsive Disorder

Primary Purpose

Obsessive Compulsive Disorder

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Cognitive behavior therapy
Mindfulness-based stress reduction
Inference-based therapy
Sponsored by
Centre de Recherche de l'Institut Universitaire en santé Mentale de Montréal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obsessive Compulsive Disorder focused on measuring Inference-based therapy, Cognitive behavior therapy, Obsessive compulsive disorder, Randomized clinical trial

Eligibility Criteria

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

Inclusion Criteria:

  • primary diagnosis according to DSM-IV-TR criteria of OCD
  • willingness to keep medication stable while participating in study
  • willingness to undergo active psychological treatment
  • willingness to undergo randomization into treatment modality
  • fluency in either English or French.
  • entry criteria do not exclude a secondary diagnosis on Axis I or II providing it does not require treatment or is deemed unlikely to significantly affect compliance with the current treatment plan.
  • participants will also be screened on a brief battery of neuropsychological tests to ensure comparability of mental capacity between groups.
  • no change in medication type or dose during the 12 weeks before treatment for antidepressants (4 weeks for anxiolytics. If antidepressant or medication as not been stable for at least 12 weeks, a stabilization period will be imposed. Other medication (e.g., anxiolytics) will have to be stable for at least four weeks.

Exclusion Criteria:

  • presence of other principal axes 1 disorders requiring treatment
  • evidence of suicidal intent
  • evidence of current substance abuse
  • evidence of current or past of suicidal intent
  • evidence of current or past schizophrenia, bipolar disorder or organic mental disorder

Sites / Locations

  • Centre de recherche de l'Institut universitaire en santé mentale de Montréal

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Experimental

Arm Label

Cognitive behavior therapy

Mindfulness-based stress reduction (MBSR)

Inference-based therapy

Arm Description

The cognitive-behavioral model is presented and individualized. Cognitive correction: beliefs are addressed by explaining their roles in maintaining cognitive biases. Next, clients are trained to identify and to challenge their key beliefs Exposure and response prevention (ERP) using imaginal and in vivo exposure and to both over and covert neutralization is implemented according to hierarchies developed following the individual assessment. Extended periods of exposure permits emotional discomfort to dissipate. Combined phase: continues ERP while making explicit links to the cognitive targets. Relapse prevention included a written individualized guide to encourage the maintenance of treatment gains. Self-directed ERP continues.

The entire intervention is based on systematic and intensive training in MBSR following Santorelli and Kabat-Zinn and their applications to everyday life. The program is divided in 8 consecutive blocks with daily homework in mindfulness-based stress reduction skills. The main activity of MBSR is a cognitive and intervention-based process characterized by self-regulation of attention to the present moment and an open and accepting orientation towards one's experience.

The inference-based therapy will be delivered in 10-step The client will: learn that the compulsions, anxiety and discomfort are driven by an initial obsessional doubt learn why this doubt is 100% irrelevant here and now learn the inferential confusion process have to recognize that the doubt originates from him/her have to identify/describe the narrative leading him/her to the doubt have to identify the cross-over point when he/she leaves reality learn to be aware of the reasoning devices learn how personal themes dictate the idiosyncratic nature of the person's obsession explore and reinforced an alternative self-view be trained to use properly his/her senses in the face of obsessional triggers situations

Outcomes

Primary Outcome Measures

Yale-Brown Obsessive-Compulsive Scale (Y-BOCS)
The Yale-Brown Obsessive-Compulsive Scale (translation) is the instrument of choice to assess obsessive compulsive symptoms and severity.

Secondary Outcome Measures

Vancouver Obsessional Compulsive Inventory (VOCI)
The Vancouver Obsessional Compulsive Inventory (VOCI)(Translation) to assess a broad spectrum of OCD symptoms and associated personality characteristics.It is a 55-item self-report measure to assess a broad spectrum of OCD symptoms and associated personality characteristics.
Obsessive Beliefs Questionnaire (OBQ-44)
The Obsessive Beliefs Questionnaire (OBQ-44) is a 44-item measure developed by the Obsessive Compulsive Cognitions Working Group between 1995 and 1998. The OBQ consist in three twinned domains based on the working group consensus (over-responsibility/over-estimation of threat, intolerance of uncertainty/over-importance of thought, control of thoughts/perfectionism).
Beck Depression Inventory (BDI)
The Beck Depression Inventory (BDI) (Translation) is a standard 21-item measure to assess depressive symptoms.
Beck Anxiety Inventory (BAI)
The Beck Anxiety Inventory (BAI)(Translation) is a standard 21-item anxiety symptom checklist rating anxiety symptom intensity for the last week on a 0-3 scale.
Over-Values Ideas Scale (OVIS)
Over-Valued Ideas Scale (OVIS)(Translation)is a 11-item clinician-rated scale measuring degree of conviction, insight, justification and actions following from belief.
Inferential Confusion Questionnaire (ICQ)
The ICQ was originally developed in French and is a 30-item questionnaire.
Semi-structured interview to assess primary inference process
Primary inference processes will be rated by semi-structured interview for each obsession on a clinical scale, and daily by the participant, in the daily diary. Strength is rated 0-100 in accordance with how probable the participant considers the primary belief whether it is a doubt "maybe the door isn't locked properly".
Mindful Attention Awareness Scale (MAAS)
The MAAS is a 15-item questionnaire which measures the tendency to be attentive and aware of present moment experience in everyday life and does not require extensive experience with mindfulness. It is uni-dimensional and is appropriate for exploring changes in awareness and attention associated with mindfulness-based stress reduction (MBSR) and is predictive of mood and adaptive regulation.
Global Assessment of Functioning (GAF) scale (DSM-IV, Axis V)
The GAF is a standard DSM measure of adaptation and functioning scored from 0-100.
Systematic Quality of Life Inventory
The Systematic Quality of Life Inventory measure 30 life domains, using three subscales: actual state, goal state and the difference between actual and desired goals of quality of life.
Life Experience Survey
The Life Experience Survey measures negative and positive life events and their impact over 57 life domains.
Social Support Questionnaire
The Social Support Questionnaire has two scales measuring amount and degree of satisfaction with social support.
Social Self-esteem Inventory
The Social Self-esteem Inventory measures agreement on 30 self-statements.

Full Information

First Posted
February 7, 2013
Last Updated
October 27, 2021
Sponsor
Centre de Recherche de l'Institut Universitaire en santé Mentale de Montréal
Collaborators
Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT01794156
Brief Title
Evaluation of a Cognitive Therapy (Inference-based-therapy) for the Treatment of Obsessional Compulsive Disorder
Official Title
Evaluation of a Cognitive Therapy (Inference-based-therapy) for the Treatment of Obsessional Compulsive Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
September 2012 (undefined)
Primary Completion Date
August 2019 (Actual)
Study Completion Date
August 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centre de Recherche de l'Institut Universitaire en santé Mentale de Montréal
Collaborators
Canadian Institutes of Health Research (CIHR)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Obsessional compulsive disorder (OCD) is a very debilitating psychiatric problem which affects around one million Canadians and their families. Obsessions are intense preoccupations about bad, harmful, dangerous, shocking or unlucky events which 'may' occur and which drive sufferers to perform time consuming and distressing compulsive rituals to prevent the possible event occurring. The current psychological treatment of choice is cognitive behavior (CBT) therapy which focuses on treating OCD by reducing obsessional anxiety about the likelihood and the consequences of the preoccupying event. A rival cognitive model termed the inference-based therapy (IBT), developed by the principal investigator and co-workers, considers that the OCD begins with the initial doubting inference 'maybe something is wrong' and focuses on changing the reasoning behind this doubting inference which often trumps the common sense conviction that there is no reason to doubt. This clinical trial randomly allocates participants to either IBT or CBT treatment condition or to a third generic mindfulness condition. The latter condition is a non-specific meditational-based training which has shown evidence of reducing stress and anxiety across a number of psychiatric problems including OCD. Two hundred and forty people will be recruited over a 5-year period from two principal sites (Montreal and Gatineau/Ottawa) with which the principal investigator and co-investigators have clinical links. Therapy will be administered by trained professionals following a treatment manual specific to each approach. The therapy will last a maximum of six months or until the point when the person achieves a non-clinical status. The patients will be assessed pre, post, and at six months following treatment on standard evaluation instruments as well as on subjective measures. We expect the IBT to be superior in terms of number of participants responding to treatment, rapidity of improvement and gains at follow-up.
Detailed Description
Obsessive compulsive disorder (OCD) affects 1-3% of the population and is the fourth most common mental disorder. It is characterized by a preoccupying obsessional doubt that harm, illness, disorder or bad luck, will occur if compulsive actions are not carried out to neutralize the risk. Treatments of choice include pharmacotherapy and cognitive behavior therapy (CBT) either alone or in combination. Although these interventions are clinically effective, they usually do not reduce the obsessions to a sub-clinical level. There is a risk of relapse and even so a sizeable minority of people with OCD refuse or abandon treatment, and some specific subtypes of OCD show no or minimal response. CBT-as-usual, involves principally the administration of exposure and response prevention (E/RP). A cognitive psycho-education element may by added in line with current cognitive thinking that it is the appraisal the person attributes to the initial intrusive thought with engenders obsessional distress. Such cognitive treatment will focus on modifying the anxiety and beliefs about consequences following on from the initial obsessional preoccupation. A competing cognitive model termed the inference-based approach (IBA) developed by the principal investigator and co-workers offers an account of obsessions which focuses on the reasoning producing the initial obsessional doubt as the source of the OCD. In this model the obsessing begins at the point where the person crosses over from reality into the initial obsessional doubt since the doubt is not based on real perception but on a subjective narrative misleading the person to infer doubt where no doubt is required. Over the last 10 years, experimental, clinical and psychometric research studies (independently replicated) have supported the essential claims of the IBA and have led to development of inference-based therapy (IBT). A small scale randomized clinical trial, and clinical case studies have established IBT as a 'promising' intervention (according to American Psychological Association criteria) and shown that IBT seems to offer advantages over conventional CBT, particularly for treatment-resistant cases who over-invest in their obsessional convictions. The current randomized clinical trial will compare IBT to CBT as usual, and to a third active control condition of mindfulness. Mindfulness is a generic treatment shown effective in a range of psychiatric problems which seeks to calm thoughts by redirecting mental focus through meditative distancing. The mindfulness condition is a non-specific cognitive control for any confounding effect of mood change on symptom relief. CBT follows an 'appraisal' model either through restructuring appraisals and beliefs about the obsession or by de-dramatizing anxious expectations through exposure and reality testing (combined with E/RP). IBT seeks to change the reasoning leading up to the initial inference of doubt on the principle that eliminating the doubt logically and necessarily eliminates all anticipated consequences and accompanying obsessional anxiety. All three treatments will be manualized and administered by experienced professional therapists supervised by a co-investigator with an allegiance to one of the three approaches. The three treatment models operate on distinct processes and on separable stages of the obsessional chain, so therapy components will not overlap. The principal sites chosen will be Montreal Louis-H. Lafontaine Hospital and Gatineau Pierre-Janet Hospital. A total of 80 participants will be recruited over a five-year period into each treatment modality, giving a total of 240, which will permit robust conclusions even with weak effect sizes. Outcome evaluators will be blind to treatment modality and independent of therapists. All therapy will be delivered on an individual weekly basis until significant clinical improvement or up to a maximum of 26 weeks with a 6-month follow-up post-treatment. All parameters of treatment delivery will be identical across treatments. All sessions will be audio recorded and treatment integrity will be rated independently. Outcome measures will be standard DSM-IV based clinical diagnostic scales and also psychosocial measures of end-point functioning across life domains. Treatment process variables will be continuously monitored. Refusal and attrition are calculated at 16% and analysis will include intention to treat. The hypotheses are that: (1) all treatments will be effective in improving mood and reducing symptoms; (2) the IBT will be superior in terms of: (a) its consistent impact over all types of OCD; (b) its lower rate of relapse. The RCT will be the first of its kind in comparing these three active treatments and will impact on treatment of choice for OCD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obsessive Compulsive Disorder
Keywords
Inference-based therapy, Cognitive behavior therapy, Obsessive compulsive disorder, Randomized clinical trial

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Cognitive behavior therapy
Arm Type
Active Comparator
Arm Description
The cognitive-behavioral model is presented and individualized. Cognitive correction: beliefs are addressed by explaining their roles in maintaining cognitive biases. Next, clients are trained to identify and to challenge their key beliefs Exposure and response prevention (ERP) using imaginal and in vivo exposure and to both over and covert neutralization is implemented according to hierarchies developed following the individual assessment. Extended periods of exposure permits emotional discomfort to dissipate. Combined phase: continues ERP while making explicit links to the cognitive targets. Relapse prevention included a written individualized guide to encourage the maintenance of treatment gains. Self-directed ERP continues.
Arm Title
Mindfulness-based stress reduction (MBSR)
Arm Type
Active Comparator
Arm Description
The entire intervention is based on systematic and intensive training in MBSR following Santorelli and Kabat-Zinn and their applications to everyday life. The program is divided in 8 consecutive blocks with daily homework in mindfulness-based stress reduction skills. The main activity of MBSR is a cognitive and intervention-based process characterized by self-regulation of attention to the present moment and an open and accepting orientation towards one's experience.
Arm Title
Inference-based therapy
Arm Type
Experimental
Arm Description
The inference-based therapy will be delivered in 10-step The client will: learn that the compulsions, anxiety and discomfort are driven by an initial obsessional doubt learn why this doubt is 100% irrelevant here and now learn the inferential confusion process have to recognize that the doubt originates from him/her have to identify/describe the narrative leading him/her to the doubt have to identify the cross-over point when he/she leaves reality learn to be aware of the reasoning devices learn how personal themes dictate the idiosyncratic nature of the person's obsession explore and reinforced an alternative self-view be trained to use properly his/her senses in the face of obsessional triggers situations
Intervention Type
Behavioral
Intervention Name(s)
Cognitive behavior therapy
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness-based stress reduction
Intervention Type
Behavioral
Intervention Name(s)
Inference-based therapy
Primary Outcome Measure Information:
Title
Yale-Brown Obsessive-Compulsive Scale (Y-BOCS)
Description
The Yale-Brown Obsessive-Compulsive Scale (translation) is the instrument of choice to assess obsessive compulsive symptoms and severity.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Secondary Outcome Measure Information:
Title
Vancouver Obsessional Compulsive Inventory (VOCI)
Description
The Vancouver Obsessional Compulsive Inventory (VOCI)(Translation) to assess a broad spectrum of OCD symptoms and associated personality characteristics.It is a 55-item self-report measure to assess a broad spectrum of OCD symptoms and associated personality characteristics.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Obsessive Beliefs Questionnaire (OBQ-44)
Description
The Obsessive Beliefs Questionnaire (OBQ-44) is a 44-item measure developed by the Obsessive Compulsive Cognitions Working Group between 1995 and 1998. The OBQ consist in three twinned domains based on the working group consensus (over-responsibility/over-estimation of threat, intolerance of uncertainty/over-importance of thought, control of thoughts/perfectionism).
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Beck Depression Inventory (BDI)
Description
The Beck Depression Inventory (BDI) (Translation) is a standard 21-item measure to assess depressive symptoms.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Beck Anxiety Inventory (BAI)
Description
The Beck Anxiety Inventory (BAI)(Translation) is a standard 21-item anxiety symptom checklist rating anxiety symptom intensity for the last week on a 0-3 scale.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Over-Values Ideas Scale (OVIS)
Description
Over-Valued Ideas Scale (OVIS)(Translation)is a 11-item clinician-rated scale measuring degree of conviction, insight, justification and actions following from belief.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Inferential Confusion Questionnaire (ICQ)
Description
The ICQ was originally developed in French and is a 30-item questionnaire.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Semi-structured interview to assess primary inference process
Description
Primary inference processes will be rated by semi-structured interview for each obsession on a clinical scale, and daily by the participant, in the daily diary. Strength is rated 0-100 in accordance with how probable the participant considers the primary belief whether it is a doubt "maybe the door isn't locked properly".
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Mindful Attention Awareness Scale (MAAS)
Description
The MAAS is a 15-item questionnaire which measures the tendency to be attentive and aware of present moment experience in everyday life and does not require extensive experience with mindfulness. It is uni-dimensional and is appropriate for exploring changes in awareness and attention associated with mindfulness-based stress reduction (MBSR) and is predictive of mood and adaptive regulation.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Global Assessment of Functioning (GAF) scale (DSM-IV, Axis V)
Description
The GAF is a standard DSM measure of adaptation and functioning scored from 0-100.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Systematic Quality of Life Inventory
Description
The Systematic Quality of Life Inventory measure 30 life domains, using three subscales: actual state, goal state and the difference between actual and desired goals of quality of life.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Life Experience Survey
Description
The Life Experience Survey measures negative and positive life events and their impact over 57 life domains.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Social Support Questionnaire
Description
The Social Support Questionnaire has two scales measuring amount and degree of satisfaction with social support.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Title
Social Self-esteem Inventory
Description
The Social Self-esteem Inventory measures agreement on 30 self-statements.
Time Frame
Baseline, change after 26 weeks of treatment, change after 6-month follow-up
Other Pre-specified Outcome Measures:
Title
Clinical Interview
Description
A clinical interview assesses content, form, and appraisal of obsessions as well as neutralization strategies used with the target obsession.
Time Frame
pre-treatment, post-treatment and 6 month follow-up

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: primary diagnosis according to DSM-IV-TR criteria of OCD willingness to keep medication stable while participating in study willingness to undergo active psychological treatment willingness to undergo randomization into treatment modality fluency in either English or French. entry criteria do not exclude a secondary diagnosis on Axis I or II providing it does not require treatment or is deemed unlikely to significantly affect compliance with the current treatment plan. participants will also be screened on a brief battery of neuropsychological tests to ensure comparability of mental capacity between groups. no change in medication type or dose during the 12 weeks before treatment for antidepressants (4 weeks for anxiolytics. If antidepressant or medication as not been stable for at least 12 weeks, a stabilization period will be imposed. Other medication (e.g., anxiolytics) will have to be stable for at least four weeks. Exclusion Criteria: presence of other principal axes 1 disorders requiring treatment evidence of suicidal intent evidence of current substance abuse evidence of current or past of suicidal intent evidence of current or past schizophrenia, bipolar disorder or organic mental disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frederick Aardema, Ph. D.
Organizational Affiliation
Centre de Recherche de l'Institut Universitaire en santé Mentale de Montréal
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre de recherche de l'Institut universitaire en santé mentale de Montréal
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H1N 3M5
Country
Canada

12. IPD Sharing Statement

Links:
URL
https://criusmm.ciusss-estmtl.gouv.qc.ca/fr/recherche/centres-detudes/centre-detudes-sur-les-troubles-obsessionnels-compulsifs-et-les-tics-cetoct
Description
Research center website

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Evaluation of a Cognitive Therapy (Inference-based-therapy) for the Treatment of Obsessional Compulsive Disorder

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