RecruitingPhase 2NCT04422652

Combination of Novel Therapies for CKD Comorbid Depression

Combination of Novel Therapies for CKD Comorbid Depression (CONCORD)


Sponsor

Stony Brook University

Enrollment

201 participants

Start Date

Sep 24, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

The overall goal of the study is to determine if treatment of a Major Depressive Disorder (MDD) improves the outcomes of patients with chronic kidney disease (CKD). We showed that MDD is present in 25% of CKD patients and independently associated with progression to End-Stage Kidney Disease, hospitalization, and death. Depression is also associated with lower quality of life (QOL), fatigue, poor sleep, and non-adherence to diet and medications. However, evidence for efficacy and tolerability of commonly-used antidepressant medications or nonpharmacologic treatments are limited in CKD patients. Our group was the first to conduct a double-blind randomized controlled trial for MDD treatment in 201 patients with non-dialysis CKD, and showed that sertraline, a commonly used selective serotonin reuptake inhibitor (SSRI), was no more efficacious than placebo for improving depressive symptoms. It becomes imperative to test novel strategies to treat MDD in CKD. We propose to compare with a control group, the efficacy and tolerability of two novel treatment strategies - (1) Behavioral Activation Teletherapy (BAT) for 16 weeks, with the addition of bupropion, a non-SSRI antidepressant, at 8 weeks for patients whose depression has not remitted (non-remitters); and (2) bupropion for 16 weeks, with the addition of BAT at 8 weeks for non-remitters. In Aim 1, we will investigate the efficacy and tolerability of these 2 strategies vs. control for improvement in a primary endpoint of depressive symptoms in 201 patients (67 per group) with CKD stages 3b-5 and MDD at 2 sites, randomized 1:1:1 to either strategy or a control group of Clinical Management plus placebo. We hypothesize that either approach vs. control will result in a minimal clinically important difference of 2 points improvement in depressive symptoms, as ascertained blindly by the Quick Inventory of Depressive Symptomatology. In Aim 2 we will investigate the efficacy and tolerability of 8 weeks of (1) single-blind BAT plus placebo or (2) double-blind bupropion plus Clinical Management vs. control for improvement in depressive symptoms. In Aim 3, we will compare the efficacy of these 2 treatments strategies vs. control for improvement in CKD patient-centered outcomes including a. adherence to medications and healthcare visits; b. fatigue; c. sleep; and d. overall functioning. A clinical trial is urgently needed to address the evidence gap that exists for MDD treatment in CKD patients.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a combination of treatments for people who have both chronic kidney disease (CKD) and major depression, to see whether treating both conditions together leads to better mental and physical health outcomes. **You may be eligible if...** - You are 18 or older - You have moderate-to-severe chronic kidney disease (stage 3b, 4, or 5), or had a kidney transplant at least 6 months ago - You have been diagnosed with major depressive disorder (MDD) and have moderate-to-severe symptoms - You can give informed consent **You may NOT be eligible if...** - You have significant liver disease - You have terminal lung disease or cancer - You have a seizure disorder - You are taking certain medications that interact with antidepressants (MAO inhibitors, certain heart rhythm drugs, or tricyclic antidepressants) - You cannot understand or comply with the study requirements Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGBupropion

Bupropion is an anti-depressant medication.

BEHAVIORALBehavioral activation therapy

Brief behavioral activation treatments administered via video tele-conferencing.

DRUGPlacebo

Double-blind placebo.

OTHERClinical Management

Clinical management will serve as the attention control for the Behavioral Activation Therapy intervention.


Locations(4)

Stony Brook University Medical Center

Stony Brook, New York, United States

Parkland Health and Hospital System

Dallas, Texas, United States

UT Southwestern and Affiliates

Dallas, Texas, United States

University of Washington

Seattle, Washington, United States

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NCT04422652


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