European Study of Quality of Life in Resistant OCD Patients Treated by STN DBS (EQOLOC)
Primary Purpose
Obsessive-Compulsive Disorder
Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Deep Brain Stimulation
Sponsored by
About this trial
This is an interventional treatment trial for Obsessive-Compulsive Disorder focused on measuring Deep Brain Stimulation, Quality of Life
Eligibility Criteria
Inclusion Criteria:
- OCD for > 5 years
- YBOCS> 25 and/or YBOCS sub-scale >15
- GAF< 45
- 3 or more documented SRI trials, including clomipramine (10-12 weeks at adequate dose)
- SRI augmentation for > 4 weeks with at least one antipsychotic and with one of the following: lithium, clonazepam
- Adequate trial of CBT (Exposure Therapy and Response Prevention) (intolerance or >15 sessions)
- Ability to provide informed consent
Exclusion Criteria:
- Hoarding (if the only OCD symptom)
- OCD with poor insight (BABS score > 12)
- Lifetime diagnosis of psychosis or bipolar disorder;
- Substance abuse or dependence within the previous six months;
- Baseline Montgomery and Asberg (MADRS) suicidality item (item 10) score >2;
- Current DSM-5 personality disorder of Cluster A (e.g., paranoid or schizotypal personality disorder) or B (e.g., borderline or antisocial personality disorder);
- Brain pathology, such as moderate or marked cerebral atrophy, stroke, tumor or previous neurosurgical procedures (i.e. capsulotomy etc), history of cognitive impairment and cognitive deterioration (Addenbrooke's Cognitive Examination ACE score of < 80).
- Contra-indications to surgery, anaesthesia, or MRI
- compulsory hospitalization/ care; pregnant or nursing patients
Sites / Locations
- CHU Henri MondorRecruiting
- University Hospital of Grenoble MichallonRecruiting
- Chu Nice - Hopital PasteurRecruiting
- APHP La Pitié SalpêtrièreRecruiting
- Universitätsklinikum Köln (AöR)
- Hadassah Medical Center The Hebrew University
- Karolinska University Hospital
- Hôpitaux Universitaires de GenèveRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Deep Brain Stimulation
Control group
Arm Description
DBS surgical procedure scheduled and realized
medical treatment (psycho- and pharmaco-therapy) will continue to be given and optimized according to the defined BMT strategies and criteria
Outcomes
Primary Outcome Measures
Assessment of the impact of DBS+BMT versus BMT alone on a measure of Quality of life in resistant OCD patients at 1-year follow-up
QOL assessment : scores at SF36
Secondary Outcome Measures
Psychiatric assessment n°1
clinical profile defined by score at YBOCS -Yale Brown Obsessive Compulsive Scale
Psychiatric assessment n°2
clinical profile defined by score at DYBOCS- Dimensional Yale Brown Obsessive Compulsive Scale
Psychiatric assessment n°3
clinical profile defined by score at YMRS (Young Mania Rating Scale)
Psychiatric assessment n°4
clinical profile defined by score at HAMA (Hamilton Rating Scale for Anxiety)
Psychiatric assessment n°5
clinical profile defined by score at STAI (State-Trait Anxiety Inventory)
Psychiatric assessment n°6
clinical profile defined by score at UPPS-P Impulsive Behavior Scale
Psychiatric assessment n°7
clinical profile defined by score at Clinical Global Impression (Severity of OCD)
Assessment of the impact of DBS+BMT versus BMT alone on a measure of Functioning score n°1
Functioning scores : GAF (Global assessment functioning scale)
Assessment of the impact of DBS+BMT versus BMT alone on a measure of Functioning score n°2
Functioning scores : WHODAS 2.0
side effects
Number of patients with side effects related to medical treatment, surgery and to stimulation
Psychiatric markers n°1
scores at Big Five Inventory
Psychiatric markers n°2
scores at BABS (BROWN ASSESSMENT OF BELIEFS SCALE)
Neurological markers n°3
score at UPDRS (Unified Parkinson's Disease Rating Scale)
Neuropsychological markers n°4
Score at OBQ-44 (Obsessive Beliefs Questionnaire)
Neuropsychological markers n°5
Score at MCQ (Metacognitions questionnaires)
Neuropsychological markers n°6
Score at URICA (University Rhode Island Change Assessment Scale)
Neuropsychological markers
Score at Addenbrooke Cognitive Examination (ACE) battery
Per-op electrophysiological mapping of the STN activity n°1
electrophysiological parameters at rest and during OCD provocative tests
Per-op electrophysiological mapping of the STN activity n°2
electrophysiological parameters at rest and during OCD uncertainty test
Per-op electrophysiological mapping of the STN activity n°3
electrophysiological parameters at rest and during OCD emotional test
Per-op electrophysiological mapping of the STN activity n°4
electrophysiological parameters at rest and during OCD cognitive and motor test
Assessment of the suicidal risk under DBS+BMT vs BMT in resistant OCD
Measure of suicidal risk with MADRS scale
Full Information
NCT ID
NCT02844049
First Posted
June 15, 2016
Last Updated
March 28, 2022
Sponsor
University Hospital, Grenoble
1. Study Identification
Unique Protocol Identification Number
NCT02844049
Brief Title
European Study of Quality of Life in Resistant OCD Patients Treated by STN DBS
Acronym
EQOLOC
Official Title
European Study of Quality of Life in Resistant OCD Patients Treated by STN DBS Versus Best Medical Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 2016 (Actual)
Primary Completion Date
July 2026 (Anticipated)
Study Completion Date
December 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Grenoble
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Obsessive-Compulsive Disorder (OCD) is among the most disabling psychiatric disorders as more than 40% of patients are resistant to the standard pharmacological and psychotherapy approaches and about 10% show severe disability and require institutionalization. These resistant patients may benefit from new surgical therapeutic approaches such as Deep Brain Stimulation (DBS) using high frequency stimulation of specific cerebral regions to modulate neural networks. Although promising, these results need nevertheless to be replicated and confirmed within a larger cohort of patients and considering a different main objective, instead of clinical improvement only. Indeed, despite a positive treatment response, adaptive functioning and quality of life may continue to be negatively impacted in OCD. Thus beyond symptom reduction, health-related quality of life (QoL) represents a more important objective of a treatment, as it includes both the individual's functional status and the individual's subjective perception of the impact of the illness on the patient's life. STN DBS induces significant clinical improvement, which may not be proportional to the QoL gain. Consequently, QoL appears to be a better outcome to target in the coming studies than clinical improvement alone. THe investigators thus propose a prospective study assessing the QoL changes of resistant OCD patients under STN DBS+BMT versus Best Medical Treatment (BMT) at 12 months, in order to assess the DBS induced gain in QoL in BMT-managed patients versus BMT alone.
Detailed Description
The study will focus on an innovative therapeutic strategy (DBS) and on an original objective, quality of life, which is considered to better reflect the impact of a therapeutic strategy. Moreover, the study will help to define the predictive biomarkers /biosignatures of response to STN DBS in OCD.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obsessive-Compulsive Disorder
Keywords
Deep Brain Stimulation, Quality of Life
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Deep Brain Stimulation
Arm Type
Active Comparator
Arm Description
DBS surgical procedure scheduled and realized
Arm Title
Control group
Arm Type
No Intervention
Arm Description
medical treatment (psycho- and pharmaco-therapy) will continue to be given and optimized according to the defined BMT strategies and criteria
Intervention Type
Device
Intervention Name(s)
Deep Brain Stimulation
Other Intervention Name(s)
DBS
Intervention Description
surgical procedure
Primary Outcome Measure Information:
Title
Assessment of the impact of DBS+BMT versus BMT alone on a measure of Quality of life in resistant OCD patients at 1-year follow-up
Description
QOL assessment : scores at SF36
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Psychiatric assessment n°1
Description
clinical profile defined by score at YBOCS -Yale Brown Obsessive Compulsive Scale
Time Frame
1 year
Title
Psychiatric assessment n°2
Description
clinical profile defined by score at DYBOCS- Dimensional Yale Brown Obsessive Compulsive Scale
Time Frame
1 year
Title
Psychiatric assessment n°3
Description
clinical profile defined by score at YMRS (Young Mania Rating Scale)
Time Frame
1 year
Title
Psychiatric assessment n°4
Description
clinical profile defined by score at HAMA (Hamilton Rating Scale for Anxiety)
Time Frame
1 year
Title
Psychiatric assessment n°5
Description
clinical profile defined by score at STAI (State-Trait Anxiety Inventory)
Time Frame
1 year
Title
Psychiatric assessment n°6
Description
clinical profile defined by score at UPPS-P Impulsive Behavior Scale
Time Frame
1 year
Title
Psychiatric assessment n°7
Description
clinical profile defined by score at Clinical Global Impression (Severity of OCD)
Time Frame
1 year
Title
Assessment of the impact of DBS+BMT versus BMT alone on a measure of Functioning score n°1
Description
Functioning scores : GAF (Global assessment functioning scale)
Time Frame
1 year
Title
Assessment of the impact of DBS+BMT versus BMT alone on a measure of Functioning score n°2
Description
Functioning scores : WHODAS 2.0
Time Frame
1 year
Title
side effects
Description
Number of patients with side effects related to medical treatment, surgery and to stimulation
Time Frame
1 year
Title
Psychiatric markers n°1
Description
scores at Big Five Inventory
Time Frame
1 year
Title
Psychiatric markers n°2
Description
scores at BABS (BROWN ASSESSMENT OF BELIEFS SCALE)
Time Frame
1 year
Title
Neurological markers n°3
Description
score at UPDRS (Unified Parkinson's Disease Rating Scale)
Time Frame
1 year
Title
Neuropsychological markers n°4
Description
Score at OBQ-44 (Obsessive Beliefs Questionnaire)
Time Frame
1 year
Title
Neuropsychological markers n°5
Description
Score at MCQ (Metacognitions questionnaires)
Time Frame
1 year
Title
Neuropsychological markers n°6
Description
Score at URICA (University Rhode Island Change Assessment Scale)
Time Frame
1 year
Title
Neuropsychological markers
Description
Score at Addenbrooke Cognitive Examination (ACE) battery
Time Frame
1 year
Title
Per-op electrophysiological mapping of the STN activity n°1
Description
electrophysiological parameters at rest and during OCD provocative tests
Time Frame
1 year
Title
Per-op electrophysiological mapping of the STN activity n°2
Description
electrophysiological parameters at rest and during OCD uncertainty test
Time Frame
1 year
Title
Per-op electrophysiological mapping of the STN activity n°3
Description
electrophysiological parameters at rest and during OCD emotional test
Time Frame
1 year
Title
Per-op electrophysiological mapping of the STN activity n°4
Description
electrophysiological parameters at rest and during OCD cognitive and motor test
Time Frame
1 year
Title
Assessment of the suicidal risk under DBS+BMT vs BMT in resistant OCD
Description
Measure of suicidal risk with MADRS scale
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
OCD for > 5 years
YBOCS> 25 and/or YBOCS sub-scale >15
GAF< 45
3 or more documented SRI trials, including clomipramine (10-12 weeks at adequate dose)
SRI augmentation for > 4 weeks with at least one antipsychotic and with one of the following: lithium, clonazepam
Adequate trial of CBT (Exposure Therapy and Response Prevention) (intolerance or >15 sessions)
Ability to provide informed consent
Exclusion Criteria:
Hoarding (if the only OCD symptom)
OCD with poor insight (BABS score > 12)
Lifetime diagnosis of psychosis or bipolar disorder;
Substance abuse or dependence within the previous six months;
Baseline Montgomery and Asberg (MADRS) suicidality item (item 10) score >2;
Current DSM-5 personality disorder of Cluster A (e.g., paranoid or schizotypal personality disorder) or B (e.g., borderline or antisocial personality disorder);
Brain pathology, such as moderate or marked cerebral atrophy, stroke, tumor or previous neurosurgical procedures (i.e. capsulotomy etc), history of cognitive impairment and cognitive deterioration (Addenbrooke's Cognitive Examination ACE score of < 80).
Contra-indications to surgery, anaesthesia, or MRI
compulsory hospitalization/ care; pregnant or nursing patients
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sandra David-tchouda, MD
Phone
+33476767186
Email
SDavidTchouda@chugrenoble.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Sandrine Massicot, Master
Phone
+33476768860
Email
smassicot@chu-grenoble.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mircea Polosan, MD PhD
Organizational Affiliation
University Hospital, Grenoble
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Henri Mondor
City
Creteil
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luc MALLET, MD PhD
Phone
33149813052
Email
luc.mallet@upmc.fr
First Name & Middle Initial & Last Name & Degree
Philippe DOMENECH, MD
First Name & Middle Initial & Last Name & Degree
Luc MALLET, MD PhD
Facility Name
University Hospital of Grenoble Michallon
City
Grenoble
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mircea POLOSAN, MD PhD
Phone
0033476765414
Email
MPolosan@chu-grenoble.fr
First Name & Middle Initial & Last Name & Degree
Mircea Polosan, MD PhD
First Name & Middle Initial & Last Name & Degree
Stéphan Chabardès, MD PhD
First Name & Middle Initial & Last Name & Degree
Anna Castrioto, MD
Facility Name
Chu Nice - Hopital Pasteur
City
Nice
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Denys FONTAINE, MD
Phone
04 92 03 84 50
Email
fontaine.d@chu-nice.fr
First Name & Middle Initial & Last Name & Degree
Hélène BRUCKER
Phone
04 92 03 75 57
Email
bruckert.h@chu-nice.fr
First Name & Middle Initial & Last Name & Degree
Denys FONTAINE, MD
First Name & Middle Initial & Last Name & Degree
Bruno GIORDANA, MD
Facility Name
APHP La Pitié Salpêtrière
City
Paris
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bruno Millet, MD PhD
Phone
33142162894
Email
b.millet@psl.aphp.fr
First Name & Middle Initial & Last Name & Degree
Carine KARACHI, MD
First Name & Middle Initial & Last Name & Degree
Bruno MILLET, MD PhD
Facility Name
Universitätsklinikum Köln (AöR)
City
Koln
Country
Germany
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Veerle VISSER-VANDEWALLE, MD
Phone
+49 221 478-82793
Email
veerle.visser-vandewalle@uk-koeln.de
First Name & Middle Initial & Last Name & Degree
Jens KUHN, MD PhD
First Name & Middle Initial & Last Name & Degree
Veerle VISSER-VANDEWALLE, MD
Facility Name
Hadassah Medical Center The Hebrew University
City
Jerusalem
Country
Israel
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zvi ISRAEL, MD
Email
israelz@hadassah.org.il
First Name & Middle Initial & Last Name & Degree
Renana EITAN, MD
First Name & Middle Initial & Last Name & Degree
Hagaï BERGMAN, MD
First Name & Middle Initial & Last Name & Degree
Zvi ISRAEL, MD
Facility Name
Karolinska University Hospital
City
Stockholm
Country
Sweden
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gaston SCHECHTMANN, MD PhD
Phone
+46 70 403 5999
Email
gaston.schechtmann@karolinska.se
First Name & Middle Initial & Last Name & Degree
Diana DJURFELDT, MD
First Name & Middle Initial & Last Name & Degree
Gaston SCHECHTMANN, MD PhD
Facility Name
Hôpitaux Universitaires de Genève
City
Geneve
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joao FLORES, MD
Email
Joao.FloresAlvesDosSantos@hcuge.ch
First Name & Middle Initial & Last Name & Degree
Shahan MOMJIAN, MD
First Name & Middle Initial & Last Name & Degree
Joao FLORES, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
23580175
Citation
Subramaniam M, Soh P, Vaingankar JA, Picco L, Chong SA. Quality of life in obsessive-compulsive disorder: impact of the disorder and of treatment. CNS Drugs. 2013 May;27(5):367-83. doi: 10.1007/s40263-013-0056-z.
Results Reference
background
PubMed Identifier
19005196
Citation
Mallet L, Polosan M, Jaafari N, Baup N, Welter ML, Fontaine D, du Montcel ST, Yelnik J, Chereau I, Arbus C, Raoul S, Aouizerate B, Damier P, Chabardes S, Czernecki V, Ardouin C, Krebs MO, Bardinet E, Chaynes P, Burbaud P, Cornu P, Derost P, Bougerol T, Bataille B, Mattei V, Dormont D, Devaux B, Verin M, Houeto JL, Pollak P, Benabid AL, Agid Y, Krack P, Millet B, Pelissolo A; STOC Study Group. Subthalamic nucleus stimulation in severe obsessive-compulsive disorder. N Engl J Med. 2008 Nov 13;359(20):2121-34. doi: 10.1056/NEJMoa0708514. Erratum In: N Engl J Med. 2009 Sep 3;361(10):1027.
Results Reference
background
PubMed Identifier
25085317
Citation
Kohl S, Schonherr DM, Luigjes J, Denys D, Mueller UJ, Lenartz D, Visser-Vandewalle V, Kuhn J. Deep brain stimulation for treatment-refractory obsessive compulsive disorder: a systematic review. BMC Psychiatry. 2014 Aug 2;14:214. doi: 10.1186/s12888-014-0214-y.
Results Reference
background
PubMed Identifier
24194703
Citation
Eitan R, Shamir RR, Linetsky E, Rosenbluh O, Moshel S, Ben-Hur T, Bergman H, Israel Z. Asymmetric right/left encoding of emotions in the human subthalamic nucleus. Front Syst Neurosci. 2013 Oct 29;7:69. doi: 10.3389/fnsys.2013.00069. eCollection 2013.
Results Reference
background
PubMed Identifier
26833615
Citation
Mataix-Cols D, Fernandez de la Cruz L, Nordsletten AE, Lenhard F, Isomura K, Simpson HB. Towards an international expert consensus for defining treatment response, remission, recovery and relapse in obsessive-compulsive disorder. World Psychiatry. 2016 Feb;15(1):80-1. doi: 10.1002/wps.20299. No abstract available.
Results Reference
background
PubMed Identifier
21520240
Citation
Piallat B, Polosan M, Fraix V, Goetz L, David O, Fenoy A, Torres N, Quesada JL, Seigneuret E, Pollak P, Krack P, Bougerol T, Benabid AL, Chabardes S. Subthalamic neuronal firing in obsessive-compulsive disorder and Parkinson disease. Ann Neurol. 2011 May;69(5):793-802. doi: 10.1002/ana.22222. Epub 2010 Dec 28.
Results Reference
background
PubMed Identifier
23715912
Citation
Ooms P, Mantione M, Figee M, Schuurman PR, van den Munckhof P, Denys D. Deep brain stimulation for obsessive-compulsive disorders: long-term analysis of quality of life. J Neurol Neurosurg Psychiatry. 2014 Feb;85(2):153-8. doi: 10.1136/jnnp-2012-302550. Epub 2013 May 28.
Results Reference
background
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European Study of Quality of Life in Resistant OCD Patients Treated by STN DBS
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