Cognitive Behavioural Therapy for Anxiety Disorders in PD
Parkinson's Disease, Generalized Anxiety Disorder, Social Phobia
About this trial
This is an interventional treatment trial for Parkinson's Disease focused on measuring Parkinson's disease, Cognitive Behavioural therapy, generalized anxiety disorder, social phobia, cerebral connectivity
Eligibility Criteria
Inclusion Criteria:
- Idiopathic PD according to the Queens Square Brain Bank diagnostic criteria
- Presence of clinically relevant anxiety symptoms, as operationalized by the Mini International Neuropsychiatric Inventory (MINI), sections for social phobia (F) and GAD (H), and/or a Parkinson Anxiety Scale (PAS) persistent score >9 and/or PAS avoidance score >3.
- Using a stable dose of levodopa or other antiparkinsonian medication for at least one month
- No other current psychological treatment for anxiety; pharmacotherapy (e.g., selective serotonin re-uptake inhibitors) is allowed if a stable dose is used at least 2 months prior to participation and the patient still meets inclusion criteria. During the trial the dosage should not be changed. Medication use and mental health care will be tracked throughout the study.
- Signed informed consent
Note: In order to achieve a representative study sample, patients will be included irrespective of their disease stage or their current antiparkinsonian medication.
Exclusion Criteria:
- Parkinsonian syndromes or neurodegenerative disorders other than PD
- Dementia or severe cognitive decline, operationalized as a Montreal Cognitive Assessment (MOCA) score < 24
- Contra-indications for magnetic resonance imaging
- Major depressive disorder (MDD) as defined by the criteria of a DSM-V diagnosis for MDD
- Abuse of alcohol, drugs or benzodiazepines.
Sites / Locations
- Neurology and Movement Disorders Unit, Lille University Hospital
- Maastricht University Medical Centre
Arms of the Study
Arm 1
Arm 2
Experimental
Other
Cognitive Behavioural Therapy (CBT)
Clinical monitoring
Patients who will receive CBT plus clinical monitoring will receive 10 weekly individual sessions (60-75 minutes), tailored to the preferences and needs of each patient. In each session, a registered psychologist will address specified aspects of (coping with) anxiety and related concerns with a specific focus on behaviour and thoughts associated with anxiety.
Patients assigned to clinical monitoring only will receive general education material on coping with PD symptoms and behavioural symptoms such as anxiety. In addition, they will be followed-up 1 month after baseline assessment via telephone calls to inquire about current anxiety symptoms. Patients will remain under the care of their personal physicians, who will also monitor their medical and psychiatric status. Patients who receive clinical monitoring only will be given the option to receive CBT once the trial is completed.