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Improving Symptoms and Quality of Life in Chronic Heart Failure: Pilot Study (CASA)

Primary Purpose

Chronic Heart Failure (CHF)

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Collaborative Care to Alleviate Symptoms and Adjust to Illness
Psychospiritual
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Heart Failure (CHF) focused on measuring palliative care, heart failure, delivery of health care

Eligibility Criteria

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

Inclusion Criteria:

  • eligible veterans from the Denver VAMC will have a prior primary discharge diagnosis of heart failure in the last year,
  • be at least 18 years of age, able to read and understand English,
  • have consistent access to a telephone
  • at least one of the following:

    1. Kansas City Cardiomyopathy Questionnaire (KCCQ) score less than or equal to 60;
    2. a second hospitalization for with a primary discharge diagnosis of heart failure in the last year;
    3. taking at least 80 mg oral furosemide (or equivalent) daily in a single or divided dose for at least 2 weeks;
    4. BNP greater than or equal to 250 or NT-proBNP greater than or equal to 1000; or
    5. estimated creatinine clearance 30-80 mL/min.

Exclusion Criteria:

  • previous diagnosis of dementia;
  • active substance abuse, defined as an AUDIT-C score greater than 7, two positive responses on substance abuse screening questions, or medical records indicating active substance abuse or dependence;
  • comorbid metastatic cancer, given the focus on heart failure palliative care;
  • nursing home resident; and
  • diagnosis of bipolar disorder or schizophrenia.

Sites / Locations

  • VA Eastern Colorado Health Care System, Denver, CO

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Collaborative Care to Alleviate Symptoms and Adjust to Illness

Psychospiritual

Arm Description

A palliative symptom management and psychosocial care intervention named Collaborative Care to Alleviate Symptoms and Adjust to Illness (CASA) that includes (a) evidence-based palliative symptom management of breathlessness, fatigue, and pain, provided by a nurse; (b) a 6-session structured psychosocial care protocol targeting depression and adjustment to illness, supplemented by informal (family) caregiver assessment and support, provided by a social worker or psychologist; and (c) brief weekly team meetings with the nurse, social worker/psychologist and a palliative care specialist, cardiologist, and primary care provider.

A psychospiritual intervention that is home-based, self-guided, and requires minimal resources. It will be delivered in written modular form via US Mail along with brief weekly telephone support.

Outcomes

Primary Outcome Measures

Cohort Retention
Cohort retention will be determined by examining the proportion of patients who complete the final study visit (at 3-month follow-up) over the total number of patients enrolled in the study (including deceased and lost-to-follow-up). Our goal is an 80% retention rate for this pilot study.

Secondary Outcome Measures

Was Depression Addressed?
The Patient Health Questionnaire-9 (PHQ-9) rates nine DSM-IV criteria of depression on a 0 (not at all) to 3 (nearly every day) scale. Scale range is 0-27, with depression severity scored: 0-4 (none), 5-9 (mild), 10-14 (moderate), 15-19 (moderately severe), 20-27 (severe). The suicidal item is "thoughts that you would be better off dead, or of hurting yourself in some way?"
Participation Rates
The investigators will use a CONSORT diagram to display participant flow, and determine how many of those who were approached enrolled in the trial.
Adherence to the Study Protocol (CASA Arm Only)
The investigators will calculate percentage adherence to pre-specified tasks on the intervention protocol, such as: how often is depression addressed with a treatment plan? how often are care team recommendations placed as orders in the medical record? how often are orders completed?

Full Information

First Posted
October 31, 2011
Last Updated
August 1, 2018
Sponsor
VA Office of Research and Development
Collaborators
University of Iowa
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1. Study Identification

Unique Protocol Identification Number
NCT01581008
Brief Title
Improving Symptoms and Quality of Life in Chronic Heart Failure: Pilot Study
Acronym
CASA
Official Title
Implementing Collaborative Care to Alleviate Symptoms and Adjust to Heart Failure: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
University of Iowa

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The overall goal of this study is to evaluate the pilot implementation of two palliative care interventions in veterans with chronic heart failure at the Denver VA Medical Center. This is a study of behavioral and care strategy interventions and involves no investigational drugs or devices.
Detailed Description
The investigators will examine the feasibility of two palliative care interventions designed to improve different facets of quality of life. Briefly, the two interventions are: A palliative symptom management and psychosocial care intervention named Collaborative Care to Alleviate Symptoms and Adjust to Illness (CASA) that includes evidence-based palliative symptom management of breathlessness, fatigue, and pain, provided by a nurse; a 6-session structured psychosocial care protocol targeting depression and adjustment to illness, supplemented by informal (family) caregiver assessment and support, provided by a social worker or psychologist; and brief weekly team meetings with the nurse, social worker/psychologist and a palliative care specialist, cardiologist, and primary care provider. A psychospiritual intervention that is home-based, self-guided, and requires minimal resources. It will be delivered in written modular form via US Mail along with brief weekly telephone support. The specific aims of the study are to: Examine intervention feasibility and determine preliminary estimates of intervention effect Determine patient participation rates and cohort retention Conduct a preliminary assessment of outcomes by measuring pre-post changes in quality of life, depressive symptoms, health status, life meaning, and spirituality. Obtain qualitative feedback from study participants, the persons providing the intervention, and providers/leaders in primary care, mental health, palliative care, chaplaincy, and hospital operations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Heart Failure (CHF)
Keywords
palliative care, heart failure, delivery of health care

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
31 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Collaborative Care to Alleviate Symptoms and Adjust to Illness
Arm Type
Experimental
Arm Description
A palliative symptom management and psychosocial care intervention named Collaborative Care to Alleviate Symptoms and Adjust to Illness (CASA) that includes (a) evidence-based palliative symptom management of breathlessness, fatigue, and pain, provided by a nurse; (b) a 6-session structured psychosocial care protocol targeting depression and adjustment to illness, supplemented by informal (family) caregiver assessment and support, provided by a social worker or psychologist; and (c) brief weekly team meetings with the nurse, social worker/psychologist and a palliative care specialist, cardiologist, and primary care provider.
Arm Title
Psychospiritual
Arm Type
Active Comparator
Arm Description
A psychospiritual intervention that is home-based, self-guided, and requires minimal resources. It will be delivered in written modular form via US Mail along with brief weekly telephone support.
Intervention Type
Other
Intervention Name(s)
Collaborative Care to Alleviate Symptoms and Adjust to Illness
Other Intervention Name(s)
Palliative symptom management and psychosocial care
Intervention Description
A palliative symptom management and psychosocial care intervention named Collaborative Care to Alleviate Symptoms and Adjust to Illness (CASA) that includes (a) evidence-based palliative symptom management of breathlessness, fatigue, and pain, provided by a nurse; (b) a 6-session structured psychosocial care protocol targeting depression and adjustment to illness, supplemented by informal (family) caregiver assessment and support, provided by a social worker or psychologist; and (c) brief weekly team meetings with the nurse, social worker/psychologist and a palliative care specialist, cardiologist, and primary care provider.
Intervention Type
Behavioral
Intervention Name(s)
Psychospiritual
Intervention Description
A psychospiritual intervention that is home-based, self-guided, and requires minimal resources. It will be delivered in written modular form via US Mail along with brief weekly telephone support.
Primary Outcome Measure Information:
Title
Cohort Retention
Description
Cohort retention will be determined by examining the proportion of patients who complete the final study visit (at 3-month follow-up) over the total number of patients enrolled in the study (including deceased and lost-to-follow-up). Our goal is an 80% retention rate for this pilot study.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Was Depression Addressed?
Description
The Patient Health Questionnaire-9 (PHQ-9) rates nine DSM-IV criteria of depression on a 0 (not at all) to 3 (nearly every day) scale. Scale range is 0-27, with depression severity scored: 0-4 (none), 5-9 (mild), 10-14 (moderate), 15-19 (moderately severe), 20-27 (severe). The suicidal item is "thoughts that you would be better off dead, or of hurting yourself in some way?"
Time Frame
3 months
Title
Participation Rates
Description
The investigators will use a CONSORT diagram to display participant flow, and determine how many of those who were approached enrolled in the trial.
Time Frame
7 months
Title
Adherence to the Study Protocol (CASA Arm Only)
Description
The investigators will calculate percentage adherence to pre-specified tasks on the intervention protocol, such as: how often is depression addressed with a treatment plan? how often are care team recommendations placed as orders in the medical record? how often are orders completed?
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: eligible veterans from the Denver VAMC will have a prior primary discharge diagnosis of heart failure in the last year, be at least 18 years of age, able to read and understand English, have consistent access to a telephone at least one of the following: Kansas City Cardiomyopathy Questionnaire (KCCQ) score less than or equal to 60; a second hospitalization for with a primary discharge diagnosis of heart failure in the last year; taking at least 80 mg oral furosemide (or equivalent) daily in a single or divided dose for at least 2 weeks; BNP greater than or equal to 250 or NT-proBNP greater than or equal to 1000; or estimated creatinine clearance 30-80 mL/min. Exclusion Criteria: previous diagnosis of dementia; active substance abuse, defined as an AUDIT-C score greater than 7, two positive responses on substance abuse screening questions, or medical records indicating active substance abuse or dependence; comorbid metastatic cancer, given the focus on heart failure palliative care; nursing home resident; and diagnosis of bipolar disorder or schizophrenia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Bekelman, MD MPH
Organizational Affiliation
VA Eastern Colorado Health Care System, Denver, CO
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Eastern Colorado Health Care System, Denver, CO
City
Denver
State/Province
Colorado
ZIP/Postal Code
80220
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
24329424
Citation
Bekelman DB, Hooker S, Nowels CT, Main DS, Meek P, McBryde C, Hattler B, Lorenz KA, Heidenreich PA. Feasibility and acceptability of a collaborative care intervention to improve symptoms and quality of life in chronic heart failure: mixed methods pilot trial. J Palliat Med. 2014 Feb;17(2):145-51. doi: 10.1089/jpm.2013.0143. Epub 2013 Dec 11.
Results Reference
result
PubMed Identifier
27076391
Citation
Hooker SA, Ross K, Masters KS, Park CL, Hale AE, Allen LA, Bekelman DB. Denver Spirited Heart: Mixed-Methods Pilot Study of a Psychospiritual Intervention for Heart Failure Patients. J Cardiovasc Nurs. 2017 May/Jun;32(3):226-235. doi: 10.1097/JCN.0000000000000337.
Results Reference
result

Learn more about this trial

Improving Symptoms and Quality of Life in Chronic Heart Failure: Pilot Study

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