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DTA (Dopaminergic Therapy for Anhedonia) Study

Primary Purpose

Depression, Anhedonia

Status

Completed

Phase

Phase 4

Locations

United States

Study Type

Interventional

Intervention

Carbidopa Levodopa

Placebo

About this trial

This is an interventional treatment trial for Depression focused on measuring Depression, Anhedonia

Eligibility Criteria

25 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

willing and able to give written informed consent;
men or women, 25-55 years of age
a primary diagnosis of DSM-V MD, current, as diagnosed by the SCID-I;
score >10 on the Patient Health Questionnaire [PHQ]-9
off all antidepressant or other psychotropic therapy (e.g. mood stabilizers, antipsychotics, anxiolytics, and sedative hypnotics) for at least 4 weeks prior to baseline visit (8 weeks for fluoxetine)
CRP ≥2 mg/L
Score >/=2 on the anhedonia question of Patient Health Questionnaire [PHQ]-9

Exclusion Criteria:

history or evidence (clinical or laboratory) of an autoimmune disorder ;
history or evidence (clinical or laboratory) of hepatitis B or C infection or human immunodeficiency virus infection; - history of any type of cancer requiring treatment with more than minor surgery;
unstable cardiovascular, endocrinologic, hematologic, hepatic, renal, or neurologic disease (as determined by physical examination, EKG and laboratory testing);
history of any (non-mood-related) psychotic disorder; active psychotic symptoms of any type; history or current bipolar disorder; history or current gambling disorder; substance abuse/dependence within 6 months of study entry (as determined by SCID);
active suicidal plan as determined by a score >3 on item #3 on the HAM-D; g. an active eating disorder (except for patients with binge eating disorder in whom binging is clearly associated with worsening of mood symptoms) ;
a history of a cognitive disorder
pregnancy or lactation;
chronic use of non-steroidal anti-inflammatory agents (NSAIDS) (excluding 81mg of aspirin), glucocorticoid containing medications or statins;
use of NSAIDS, glucocorticoids, or statins at any time during the study;
urine toxicology screen is positive for drugs of abuse,
any contraindication for MRI scanning; n. intolerance, sensitivity or contraindication to carbidopa-levodopa (including history of narrow-angle glaucoma, melanoma, gastric and/or duodenal ulcers, bleeding disorders, or frequent migraines).

Sites / Locations

Emory University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Arm Label

Carbidopa Levodopa followed by Placebo

Placebo followed by Carbidopa Levodopa

Arm Description

Participants will receive first Carbidopa Levodopa at doses ranging from 150 to 450 mg administered at a ratio of 1 mg carbidopa for every 4 mg L-DOPA with a starting dose of 150 mg/day with dose escalation 150 mg/day per week to a final dose of 450 mg/day; and then placebo.

Participants will receive first placebo, and then Carbidopa Levodopa (L-DOPA) at doses ranging from 150 to 450 mg administered at a ratio of 1 mg carbidopa for every 4 mg L-DOPA with a starting dose of 150 mg/day with dose escalation 150 mg/day per week to a final dose of 450 mg/day.

Outcomes

Primary Outcome Measures

Change in targeted ventral striatum to ventromedial prefrontal cortex (VS-vmPFC) connectivity

Patients will undergo resting-state and task-based functional magnetic resonance imaging (fMRI) to calculate functional connectivity (FC) between the ventral striatum (VS) and ventromedial prefrontal cortex (vmPFC). FC is measured as continuous Z scores reflecting the correlation of activity between the brain regions. Higher FC Z scores reflect stronger connectivity.

Secondary Outcome Measures

Change in Effort-Expenditure for Rewards Task (EEfRT)

The EEfRT is a widely used, multi-trial task in which participants are given an opportunity on each trial to choose between two different task difficulty levels in order to obtain monetary rewards. EEfRT will be used as an objective measure of motivation and will be administered following MRI scans during the study. The EEfRT is reported as the percent of high effort trials selected. A higher percentage reflects higher motivation for effort expenditure.

Change in Inventory of Depressive Symptomatology- Self-Report (IDS-SR)

Anhedonia will be assessed from a subscale of the Inventory of Depressive Symptomatology- Self-Report (IDS-SR). Scores on this 3-question scale range from 0-9 with higher scores reflecting greater anhedonia.

Change in Snaith-Hamilton Pleasure Scale-Clinician (SHAPS-C )

The Snaith-Hamilton Pleasure Scale-Clinician (SHAPS-C) is a clinician administered tool to assess symptoms of anhedonia. The SHAPS-C uses 14 question each rated on a Likert scale of 1-4, with higher scores reflecting greater pathology.

Change in Motivation and Pleasure-Self-Report (MAP-SR)

The Motivation and Pleasure-Self-Report (MAP-SR) will be used to capture self-reported aspects of anhedonia and reduced motivation. The scale uses 18 question each rated on a Likert scale of 0-4, with higher scores reflecting greater pathology.

Change in Hamilton Depression Rating Scale (HAM-D)

The anhedonia and motivation-related item from the clinician administered Hamilton Depression Rating Scale (HAM-D) (item #7: work and activities) will be used to measure anhedonia. This item is rated on a scale of 0-4 with higher scores reflecting greater pathology

Full Information

NCT ID

NCT04723147

First Posted

January 21, 2021

Last Updated

October 24, 2023

Sponsor

Emory University

Collaborators

National Institute of Mental Health (NIMH)

1. Study Identification

Unique Protocol Identification Number

NCT04723147

Brief Title

DTA (Dopaminergic Therapy for Anhedonia) Study

Official Title

Dopaminergic Therapy for Inflammation-Related Anhedonia in Depression

Study Type

Interventional

2. Study Status

Record Verification Date

October 2023

Overall Recruitment Status

Completed

Study Start Date

January 29, 2021 (Actual)

Primary Completion Date

October 11, 2023 (Actual)

Study Completion Date

October 11, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Principal Investigator

Name of the Sponsor

Emory University

Collaborators

National Institute of Mental Health (NIMH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Yes

Studies a U.S. FDA-regulated Device Product

Product Manufactured in and Exported from the U.S.

Data Monitoring Committee

Yes

5. Study Description

Brief Summary

The purpose of this 6-week, double-blind, placebo-controlled, crossover study is to explore new treatment options for people with depression who have high inflammation and anhedonia. Thirty-five male and female participants with depression, between the ages of 25-55 years of age, will be randomized to two study tracks (A and B) to receive both placebo and three doses of L-DOPA, given in different orders. Increases or decreases in each dose will occur gradually over 6 weeks of the study. Participants will complete lab tests, medical and psychiatric assessments, neurocognitive testing and functional MRI (fMRI) scans as part of the study. The total length of participation is about 2 months.

Detailed Description

Depression is a widespread disorder (lifetime prevalence >20%). Current antidepressant medications are effective for many patients; however, more than 30% fail to respond. Of the patients that do respond to treatment, some continue to suffer with primary symptoms of depression like an inability to experience pleasure, called anhedonia. In this regard, one biological pathway that may contribute to symptoms of depression and particularly anhedonia is inflammation. The purpose of this 6-week, double-blind, placebo-controlled, crossover study is to explore new treatment options for people with depression who have high inflammation and anhedonia. Despite evidence of low dopamine function in patients with depression, the ability of existing dopaminergic therapies, like L-DOPA, to affect brain circuits in depression has yet to be explored. This study will help determine the best dose of an FDA-approved medication, Sinemet (L-DOPA) that might be used in the future to treat sub-groups of depressed individuals. Forty male and female participants with depression, between the ages of 25-55 years of age, will be randomized to two study tracks (A and B) to receive both placebo and three doses of L-DOPA, given in different orders. Increases or decreases in each dose will occur gradually over 6 weeks of the study. Participants will complete lab tests, medical and psychiatric assessments, neurocognitive testing and functional MRI (fMRI) scans as part of the study. The total length of participation is about 2 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Depression, Anhedonia

Keywords

Depression, Anhedonia

7. Study Design

Primary Purpose

Treatment

Study Phase

Phase 4

Interventional Study Model

Crossover Assignment

Masking

ParticipantInvestigator

Allocation

Randomized

Enrollment

20 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Carbidopa Levodopa followed by Placebo

Arm Type

Experimental

Arm Description

Arm Title

Placebo followed by Carbidopa Levodopa

Arm Type

Experimental

Arm Description

Intervention Type

Drug

Intervention Name(s)

Carbidopa Levodopa

Other Intervention Name(s)

Sinemet, L-DOPA

Intervention Description

Patients will receive L-DOPA at doses ranging from 150 to 450 mg administered at a ratio of 1 mg carbidopa for every 4 mg L-DOPA. Starting dose is 150 mg/day with dose escalation 150 mg/day per week to a final dose of 450 mg/day

Intervention Type

Drug

Intervention Name(s)

Placebo

Other Intervention Name(s)

Placebo tablet

Intervention Description

A placebo is a sugar pill that has no therapeutic effect and will be administered orally. Participants will receive 1 placebo tablet matching the Carbidopa Levodopa tablet.

Primary Outcome Measure Information:

Title

Change in targeted ventral striatum to ventromedial prefrontal cortex (VS-vmPFC) connectivity

Description

Time Frame