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Reward Function and Therapy for Late-Life Depression

Not Applicable
Completed
Conditions
Major Depressive Disorder
Interventions
Behavioral: Engage Therapy
Behavioral: Supportive Therapy
Registration Number
NCT03688139
Lead Sponsor
Weill Medical College of Cornell University
Brief Summary

The goal of this study is to learn about changes in the brain that occur during Engage, a psychotherapy for depression in older adults, and how they may differ from changes that occur during supportive therapy. Older adults with depression will receive 9 weeks of either Engage or supportive therapy and will complete research assessments before the therapy begins and at weeks 3, 6, and 9 of treatment. Research assessments will include questionnaires, computer tasks, and recordings of electrical brain activity (also called electroencephalography or EEG).

Detailed Description

Late-life depression is prevalent and devastating, and response rates to even the most effective treatments are low. Outcomes may be improved by developing targeted interventions such as Engage - a new, easily disseminated, neurobiologically informed psychotherapy for late-life depression designed to restore impaired function of neural reward systems. This study will use event-related potentials and a panel of other reward system measures to assess target engagement in depressed older adults receiving Engage therapy, with a comparison group of depressed peers receiving supportive therapy. Participants will be randomly assigned to either Engage or supportive therapy and will complete research assessments at baseline and weeks 3, 6, and 9 (end of treatment).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
65
Inclusion Criteria
  • Age greater than or equal to 60 years.
  • Diagnosis of unipolar major depressive disorder without psychotic features, determined by Structured Clinical Interview for the Diagnostic and Statistical Manual for Mental Disorders (SCID).
  • Montgomery-Asberg Depression Rating Scale (MADRS) score greater than or equal to 20.
  • Mini Mental State Exam (MMSE) score greater than or equal to 24.
  • Off antidepressants or on a stable dose of an antidepressant for 12 weeks and no intent to change the dose in the next 10 weeks.
  • Capacity to provide written consent for both research assessment and treatment.
Exclusion Criteria
  • Intent or plan to attempt suicide in the near future.
  • Presence of current psychiatric diagnoses other than major depressive disorder without psychotic features, generalized anxiety disorder, or specific phobia.
  • History of past psychiatric diagnoses other than major depressive disorder without psychotic features or anxiety disorders (separation anxiety disorder, specific phobia, social phobia, panic disorder, agoraphobia, or generalized anxiety disorder).
  • Use of psychotropic drugs or cholinesterase inhibitors other than use of less than or equal to 0.5 mg of lorazepam daily up to five times per week.
  • Neurological disorders (dementias, history of stroke, multiple sclerosis, Parkinson's disease, epilepsy, etc.); cardiac, renal, or respiratory failure; severe chronic obstructive pulmonary disease; metastatic cancer; or debilitated states or less common medical illnesses that may either influence neural systems of interest or ability to participate in the study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Engage TherapyEngage TherapyParticipants receive Engage therapy for 9 weeks.
Supportive TherapySupportive TherapyParticipants receive supportive therapy for 9 weeks.
Primary Outcome Measures
NameTimeMethod
Change in Late Positive Potential to Rewarding StimuliChange from baseline to week 9

The late positive potential (LPP) is an electroencephalographic (EEG)-derived measure of emotional engagement with positively valanced images.

Change in the Reward PositivityChange from baseline to week 9

The reward positivity (RewP) is an electroencephalographic (EEG)-derived response to rewarding feedback from a guessing task.

Change in P1Change from baseline to week 9

The P1 is an electroencephalographic (EEG)-derived measure of early visual attention that is elicited by visual stimuli.

Change in Behavioral ActivationChange from baseline to week 9

Behavioral activation will be measured using the Behavioral Activation for Depression Scale (BADS), a 25-item measure of behaviors targeted in behavioral activation therapies such as Engage. Scores range from 0 to 150, where higher scores on this measure indicate more participation in activities and social interactions, and lower scores indicate more social isolation, rumination, and avoidance of activities.

Secondary Outcome Measures
NameTimeMethod
Change in AnhedoniaChange from baseline to week 9

Anhedonia will be measured by the clinician-rated Snaith-Hamilton Pleasure Scale (SHAPS-C). The SHAPS-C measures pleasure and enjoyment experienced in response to a variety of situations. Scores range from 14 to 56, where higher scores indicate greater severity of anhedonia and lower scores indicate lower severity of anhedonia.

Trial Locations

Locations (1)

Weill Cornell Medicine

🇺🇸

White Plains, New York, United States

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