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Improving Quality of Life in Heart Failure

Improving Quality of Life in Outpatients With Heart Failure: A Two-arm Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03288194
Enrollment
14
Registered
2017-09-19
Start date
2015-10-31
Completion date
2017-04-24
Last updated
2022-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure, Quality of Life

Brief summary

This research study has been designed to test the efficacy of telephone-delivered Problem-Solving Treatment (PST) for improving the quality of life (QoL) in outpatients with stable heart failure (HF).

Detailed description

Heart failure (HF) is the end stage of all cardiovascular diseases, and it imposes a huge burden in the United States in terms of morbidity, mortality, and economic cost. Although disease management programs have been developed to curb these costs and address the complexities of HF management, evaluations of these programs have yielded equivocal results. With this study the Investigators plan to: (1) to determine the feasibility of telephone delivered PST for outpatients with HF and reduced QoL by obtaining estimates of yield, retention, patient acceptance, and patient satisfaction; (2) to determine whether telephone-delivered PST is associated with greater improvements in QoL than telephone-delivered Time Management over 8 weeks; and (3) to determine whether telephone-delivered PST is associated with greater reductions in depressive symptoms and/or greater improvements in self-efficacy or objectively assessed daily physical activity than telephone-delivered Time Management over 8 weeks.

Interventions

BEHAVIORALTime Management

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Outpatient * Age \> 21 * Exhibits symptoms of hear failure (NYHA Class II or III) * Left ventricular ejection fraction (LVEF) \>= 40% * Kansas City Cardiomyopathy Questionnaire (KCCQ) summary score \< 60

Exclusion criteria

* Cannot speak English * Lack telephone access * Unwilling to be randomized, or * Unavailable for the study period * Awaiting a heart transplant (United Network for Organ Sharing Status 1A or 1B), or * Planned (within 6 months) cardiac surgery * Cognitive impairment indicative of dementia * Recent (3 months) * acute myocardial infarction, * cardiac decompensation, or * HF-related hospitalization. * Use intravenous inotropic medication * Use an assistive circulatory device * Significantly reduced life expectancy due to co-morbidity (e.g., malignancy) * Currently receiving mental health counseling; * A history of: * bipolar disorder, * psychosis, or * substance abuse/dependency * Severe depressive symptoms or suicidality

Design outcomes

Primary

MeasureTime frameDescription
Change in Kansas City Cardiomyopathy Questionnaire1 month, 2 months, 3 months, 4 months, 5 monthsThe Kansas City Cardiomyopathy Questionnaire is a 23-item, self-administered instrument that quantifies physical function, symptoms (frequency, severity and recent change), social function, self-efficacy and knowledge, and quality of life.

Secondary

MeasureTime frameDescription
Change in Beck Depression Inventory1 month, 2 months, 3 months, 4 months, 5 monthsThe Beck Depression Inventory is a 21-question multiple-choice self-report inventory, one of the most widely used psychometric tests for measuring the severity of depression.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026