Combination of Novel Therapies for CKD Comorbid Depression

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorStony Brook University

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female adults aged 18 years or greater. There will be no upper age limit.

Presence of CKD stages 3b, 4 or 5, with an estimated glomerular filtration rate (GFR) of <45 mL/min/1.73 m2 for a period of at least 3 months, as defined by the National Kidney Foundation and determined using the four-variable Modification of Diet for Renal Diseases Study formula.

Presence of a current Major Depressive Disorder (MDD) based on MINI DSM IV-based criteria

Quick Inventory of Depressive Symptomatology-Self-report (QIDS-SR) score of ≥11 at enrollment and ≥11 on QIDS-Clinician Rated (QIDS-C) at randomization.

Disqualifiers

Unable to understand or give informed consent.

Unwilling or unable to participate in the protocol or comply with any of its components

Significant hepatic dysfunction or liver enzyme abnormalities 3 times or greater than the upper limit of normal

Terminal chronic obstructive pulmonary disease or cancer

Trial design

Design model

Parallel

Treatments tested in this trial

  • Bupropion

    Drug

    Bupropion is an anti-depressant medication.

  • Behavioral activation therapy

    Behavioral

    Brief behavioral activation treatments administered via video tele-conferencing.

  • Placebo

    Drug

    Double-blind placebo.

  • Clinical Management

    Other intervention

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

Treatment groups

201 Participants
are divided into 3 treatment groups
Group A: Strategy 1Active comparator 2 interventions
Group B: Strategy 2Active comparator 2 interventions
Group C: ControlPlacebo comparator 2 interventions

Trial outcomes

Primary outcomes

1

Quick Inventory of Depressive Symptomatology-Clinician Rated scale (QIDS-C)

Assess the change from baseline in the QIDS-C total score in each of the intervention arms vs. the control arm. The score on the QIDS-C ranges from 0-27, with higher scores indicating more severe depressive symptoms.

Time frame
Assessed at baseline and weeks 4, 6, 8, 12, and 16

Secondary outcomes

1

Serious adverse events

Pre-specified serious adverse events include death, hospitalization, renal replacement therapy (dialysis or kidney transplantation), and acute suicidal intent.

Time frame
Assessed at weeks 4, 6, 8, 12, and 16.
2

Quick Inventory of Depressive Symptomatology-Clinician Rated scale (QIDS-C)

Assess the change from baseline in the QIDS-C total score in each of the intervention arms vs. the control arm during the first 8 weeks of the study when participants in the treatment arms will be receiving monotherapy with BAT or bupropion.

Time frame
Assessed at baseline and weeks 4, 6, and 8.
3

Serious adverse events with monotherapy

Pre-specified serious adverse events include death, hospitalization, renal replacement therapy (dialysis or kidney transplantation), and acute suicidal intent during the first 8 weeks of the study.

Time frame
Assessed at weeks 4, 6, and 8.
4

Quick Inventory of Depressive Symptomatology-Clinician Rated scale (QIDS-C)

Assess the change from baseline in the QIDS-C total score in each of the intervention arms vs. the control arm during the second 8 weeks of the study when participants who did not respond to the treatment arms will be receiving combination therapy with BAT and bupropion.

Time frame
Assessed at weeks 8, 12, and 16.

Other outcomes

Sponsors and contacts

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Stony Brook University

Lead sponsor

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborator