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Antidepressant Medication Treatment for Depression in Individuals With Chronic Heart Failure (SADHART-CHF)

Primary Purpose

Heart Failure, Congestive, Chronic Heart Failure, Depression

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Sertraline
Placebo
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure, Congestive focused on measuring Antidepressive Agents

Eligibility Criteria

45 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Chronic heart failure Diagnostic and Statistical Manual- Fourth Edition (DSM-IV) criteria for major depression Current use of any antipsychotic medication at study entry Exclusion Criteria: Life-threatening comorbidity with a 50% or higher likelihood of death within 1 year History of psychoses, bipolar disorder, or severe personality disorder History of alcohol or drug dependence in the last year Severe physical disability that may interfere with the study Neurological impairment Active suicidal ideations Current use of antidepressant medication(s) at the start of study medication

Sites / Locations

  • Duke Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Sertraline

Placebo

Arm Description

Participants will take sertraline for 12 weeks

Participants will take placebo for 12 weeks

Outcomes

Primary Outcome Measures

Symptoms of Depression in Congestive Heart Failure Patients With Clinical Depression After Treatment With Sertraline or Placebo
Symptoms of depression (as measured by the Hamilton Depression Rating Scale, HDRS) in congestive heart failure patients with clinical depression after treatment with sertraline or placebo. The 17-item Hamilton Depression Rating Scale (HDRS) is a rater-administered assessment of depression severity, with total score ranges from 0 (not at all depressed) to 52 (most severely depressed). Change in depression was measured as the difference between the 12-week HDRS scores and the baseline HDRS scores. Thus, a negative value reflects an improvement in depressive symptoms over the 12-week period.

Secondary Outcome Measures

Percentage of Cardiac Events and Morbidity / Mortality, Including Rehospitalization, in Congestive Heart Failure Patients With Depression After Treatment With Sertraline or Placebo.
Composite cardiovascular scores are calculated for each participant using recorded cardiac events, morbidity/mortality, rehospitalization, and discontinuation due to cardiovascular events. Composite score is compared for sertraline and placebo treatment groups.

Full Information

First Posted
February 20, 2004
Last Updated
January 23, 2013
Sponsor
Duke University
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00078286
Brief Title
Antidepressant Medication Treatment for Depression in Individuals With Chronic Heart Failure
Acronym
SADHART-CHF
Official Title
Safety and Efficacy of Sertraline for Depression CHF
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
November 2003 (undefined)
Primary Completion Date
March 2008 (Actual)
Study Completion Date
September 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will examine the effect of antidepressant medication on rates of death and disease in depressed people with chronic heart failure.
Detailed Description
Comorbid depression in people with chronic medical illness is a serious public health concern. Depressive disorders lead to increased morbidity, mortality, and poorer outcomes in ischemic heart disease, a leading cause of chronic heart failure (CHF). Evidence suggests that a relationship exists between depression and CHF; studies that examine the way CHF is affected by depression treatments are needed. Participants in this study will be randomly assigned to receive either sertraline or placebo for 12 weeks. Assessments will be made at Weeks 2, 4, 6, 8, 10, and 12. Participants who do not respond to their treatment will have their medication dose adjusted following assessment. Interviews and rating scales will be used to assess depressive symptoms, cognitive status, psychiatric comorbidity, daily and chronic stress, and social support. A follow-up visit will take place 6 months, 1 year, 2 years, and 3 years after study completion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Congestive, Chronic Heart Failure, Depression
Keywords
Antidepressive Agents

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
469 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sertraline
Arm Type
Experimental
Arm Description
Participants will take sertraline for 12 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Participants will take placebo for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Sertraline
Other Intervention Name(s)
Zoloft
Intervention Description
Dosage ranging from 50 mg to 200 mg once a day
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Inactive pill
Intervention Description
Dosage ranging from 50 mg to 200 mg once a day
Primary Outcome Measure Information:
Title
Symptoms of Depression in Congestive Heart Failure Patients With Clinical Depression After Treatment With Sertraline or Placebo
Description
Symptoms of depression (as measured by the Hamilton Depression Rating Scale, HDRS) in congestive heart failure patients with clinical depression after treatment with sertraline or placebo. The 17-item Hamilton Depression Rating Scale (HDRS) is a rater-administered assessment of depression severity, with total score ranges from 0 (not at all depressed) to 52 (most severely depressed). Change in depression was measured as the difference between the 12-week HDRS scores and the baseline HDRS scores. Thus, a negative value reflects an improvement in depressive symptoms over the 12-week period.
Time Frame
Measured at Week 12
Secondary Outcome Measure Information:
Title
Percentage of Cardiac Events and Morbidity / Mortality, Including Rehospitalization, in Congestive Heart Failure Patients With Depression After Treatment With Sertraline or Placebo.
Description
Composite cardiovascular scores are calculated for each participant using recorded cardiac events, morbidity/mortality, rehospitalization, and discontinuation due to cardiovascular events. Composite score is compared for sertraline and placebo treatment groups.
Time Frame
Measured at Week 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chronic heart failure Diagnostic and Statistical Manual- Fourth Edition (DSM-IV) criteria for major depression Current use of any antipsychotic medication at study entry Exclusion Criteria: Life-threatening comorbidity with a 50% or higher likelihood of death within 1 year History of psychoses, bipolar disorder, or severe personality disorder History of alcohol or drug dependence in the last year Severe physical disability that may interfere with the study Neurological impairment Active suicidal ideations Current use of antidepressant medication(s) at the start of study medication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ranga Krishnan, PhD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duke Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20723799
Citation
O'Connor CM, Jiang W, Kuchibhatla M, Silva SG, Cuffe MS, Callwood DD, Zakhary B, Stough WG, Arias RM, Rivelli SK, Krishnan R; SADHART-CHF Investigators. Safety and efficacy of sertraline for depression in patients with heart failure: results of the SADHART-CHF (Sertraline Against Depression and Heart Disease in Chronic Heart Failure) trial. J Am Coll Cardiol. 2010 Aug 24;56(9):692-9. doi: 10.1016/j.jacc.2010.03.068.
Results Reference
result
PubMed Identifier
26186432
Citation
Xiong GL, Prybol K, Boyle SH, Hall R, Streilein RD, Steffens DC, Krishnan R, Rogers JG, O'Connor CM, Jiang W; SADHART-CHF Investigators. Inflammation Markers and Major Depressive Disorder in Patients With Chronic Heart Failure: Results From the Sertraline Against Depression and Heart Disease in Chronic Heart Failure Study. Psychosom Med. 2015 Sep;77(7):808-15. doi: 10.1097/PSY.0000000000000216.
Results Reference
derived
PubMed Identifier
20101071
Citation
Steffens DC, Wei Jiang, Krishnan KR, Karoly ED, Mitchell MW, O'Connor CM, Kaddurah-Daouk R. Metabolomic differences in heart failure patients with and without major depression. J Geriatr Psychiatry Neurol. 2010 Jun;23(2):138-46. doi: 10.1177/0891988709358592. Epub 2010 Jan 25.
Results Reference
derived
PubMed Identifier
18760123
Citation
Jiang W, O'Connor C, Silva SG, Kuchibhatla M, Cuffe MS, Callwood DD, Zakhary B, Henke E, Arias RM, Krishnan R; SADHART-CHF Investigators. Safety and efficacy of sertraline for depression in patients with CHF (SADHART-CHF): a randomized, double-blind, placebo-controlled trial of sertraline for major depression with congestive heart failure. Am Heart J. 2008 Sep;156(3):437-44. doi: 10.1016/j.ahj.2008.05.003. Epub 2008 Jul 7.
Results Reference
derived

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Antidepressant Medication Treatment for Depression in Individuals With Chronic Heart Failure

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