Depression Clinical Trial
Official title:
Treating Depression in Parkinson's Disease: A New Method
The purpose of this study is to evaluate the efficacy of a cognitive-behavioral treatment,
that includes a caregiver-focused social support intervention, for depression in persons
with Parkinson's disease.
Individuals who are unable to travel to the study site, but are interested in participating
and meet all other eligibility requirements, will be allowed to participate over the phone.
Depression is the most common emotional problem found in persons with Parkinson's disease
(PD). It causes immense personal suffering and is associated with increased disability and
burden to caregivers. Despite the adverse consequences of depression in PD, there are
virtually no studies to guide clinical treatment. Several studies are currently examining
the effectiveness of antidepressant medication for depression in PD. However, there have
been no studies to examine the effectiveness of non-medication approaches, such as
cognitive-behavioral therapy, despite the success of these techniques in other populations.
Cognitive-behavioral therapy teaches people with PD to become more aware of their thoughts
and feelings and to change thinking patterns and behaviors that may be related to symptoms
of depression.
The purpose of this study is to determine if cognitive-behavioral therapy—-with a
caregiver-focused social support intervention—-is effective in treating depression in
persons with PD. This study will enroll 80 people with PD and their caregivers. Forty
participants with PD will be randomly chosen to receive the study treatment in addition to
standard medical care. The other 40 will only receive standard medical care and will have
the option to receive the study treatment after completing all study assessments (4 months
after the initial evaluation).
The study treatment will consist of 10 weekly individual cognitive-behavioral treatment
sessions, lasting 1 hour each and modified to meet the unique needs of each individual with
PD. Caregivers will attend 4 separate educational sessions—lasting 30 minutes each—-designed
to provide them with the tools needed to reinforce and supplement the material presented in
the cognitive-behavioral sessions. Duration of the study for participants is 15 weeks.
This is the first study to evaluate the impact of a cognitive-behavioral treatment for PD
depression in a randomized controlled trial. Information gained from this study may be
beneficial in treating depression in persons with PD.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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