Skip to content

Study for Breathing Interventions in Congestive Heart Failure

Pilot Study for Breathing Interventions in Congestive Heart Failure

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03449121
Enrollment
0
Registered
2018-02-28
Start date
2018-11-30
Completion date
2019-05-31
Last updated
2019-03-04

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

Conditions

Congestive Heart Failure

Keywords

Breathing, Mind-body

Brief summary

Slow breathing may reduce stress. Adults with congestive heart failure have higher stress than the general population. This study will examine if using slow breathing is feasible among adults with heart failure.

Interventions

BEHAVIORALSlow breathing techniques

8 sessions of instruction in slow breathing exercises over 12 weeks of study

Sponsors

Vanderbilt University Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Documented heart failure from medical chart review with signs and symptoms consistent with disease * Reduced left ventricular function with ejection fraction of less than or equal to 40% * English speaking

Exclusion criteria

* New York Heart Failure Association Class I or IV * Myocardial infarction in the last 3 months * Cardiac surgery in the last 3 months * Significant valvular heart disease * Uncontrolled cardiac arrhythmias * Uncontrolled diabetes mellitus (hemoglobin a1c ≥ 8) * Uncontrolled hypertension * Systolic greater than 140 mmHg * Diastolic greater than or 90 mmHg * Cognitive impairment (Mini-mental state exam less than or equal to 24) * Acute major depression in the last 3 months * Other psychiatric conditions including schizophrenia or bipolar disorder * Attention-deficit-disorder or attention-deficit-hyperactivity disorder * Musculoskeletal condition limiting capacity to perform simple movements such as significant chronic lower back pain or neck pain * Unstable or severe chronic lung conditions * Current participation in a mind-body practice/program * Current cancer other than non-melanoma skin cancer * Regular swimmer * Plays wind or brass musical instruments

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of intervention administration measured by patient satisfactionOne time, at 12 week surveyA survey will be administered that assesses participant satisfaction with the yoga. Overall satisfaction will be assessed by Very Unsatisfied, Unsatisfied, Satisfied, Very Satisfied.
Safety of yoga practice as measured by occurrence of adverse eventsWeekly for 12 weeksInvestigators will monitor for adverse events related to yoga practice during the intervention and will solicit any adverse events during home practice since last meeting.
Feasibility of intervention administration measured by frequency of visitsWeekly for 12 weeksInvestigators will document weekly attendance
Feasibility of intervention administration measured by home practice adherenceWeekly for 12 weeksInvestigators will ask participants how often they practiced yoga at home since last session

Secondary

MeasureTime frameDescription
Magnitude of change in PROMIS Fatigue scaleBaseline, 6 week, 12 weekPatient-Reported Outcomes Measurement Information System (PROMIS) Fatigue Computer Adaptive Test (CAT). The PROMIS Fatigue instruments evaluate a range of self-reported symptoms, from mild subjective feelings of tiredness to an overwhelming, debilitating, and sustained sense of exhaustion that likely decreases one's ability to execute daily activities and function normally in family or social roles. With CAT, participant responses guide the system's choice of subsequent items from the full item bank (95 items in total) and a T-Score is generated. T-Score distributions are standardized such that a 50 represents the average (mean) for the US general population, and the standard deviation around that mean is 10 points. A higher score reflects higher levels of fatigue.
Magnitude of change in PROMIS Depression scaleBaseline, 6 week, 12 weekPatient-Reported Outcomes Measurement Information System (PROMIS) Depression Computer Adaptive Test (CAT). The PROMIS Depression instruments assess self-reported negative mood (sadness, guilt), views of self (selfcriticism, worthlessness), and social cognition (loneliness, interpersonal alienation), as well as decreased positive affect and engagement (loss of interest, meaning, and purpose). With CAT, participant responses guide the system's choice of subsequent items from the full item bank (28 items in total) and a T-Score is generated. T-Score distributions are standardized such that a 50 represents the average (mean) for the US general population, and the standard deviation around that mean is 10 points. A higher score reflects higher levels of depression.
Autonomic toneMonthly data extraction from ICD: Baseline, week 4, week 8, week 12The investigators will estimate autonomic tone of participants by extracting data from implantable cardioverter defibrillator (ICD). Data analyses will consist of heart rate spectral analyses.
Magnitude of change in PROMIS Dyspnea scaleBaseline, 6 week, 12 weekPatient-Reported Outcomes Measurement Information System (PROMIS) Dyspnea Severity Computer Adaptive Test (CAT). The PROMIS Dyspnea instruments evaluate a range of self-reported symptoms related to dyspnea. With CAT, participant responses guide the system's choice of subsequent items from the full item bank (33 items in total) and a T-Score is generated. T-Score distributions are standardized such that a 50 represents the average (mean) for the US general population, and the standard deviation around that mean is 10 points. A higher score reflects higher levels of dyspnea.
Magnitude of change in PROMIS Anxiety scaleBaseline, 6 week, 12 weekPatient-Reported Outcomes Measurement Information System (PROMIS) Anxiety Computer Adaptive Test (CAT). The PROMIS Anxiety instruments measure self-reported fear (fearfulness, panic), anxious misery (worry, dread), hyperarousal (tension, nervousness, restlessness), and somatic symptoms related to arousal (racing heart, dizziness). With CAT, participant responses guide the system's choice of subsequent items from the full item bank (29 items in total) and a T-Score is generated. T-Score distributions are standardized such that a 50 represents the average (mean) for the US general population, and the standard deviation around that mean is 10 points. A higher score reflects higher levels of anxiety.
Magnitude of change in PROMIS Global Health scaleBaseline, 6 week, 12 weekPatient-Reported Outcomes Measurement Information System (PROMIS) Global Health. The PROMIS Global Health measures assess an individual's physical, mental, and social health. Each of the 10 items are totaled into a raw sum score and Raw Sum Scores are then converted into T-Scores. T-Score distributions are standardized such that a 50 represents the average (mean) for the US general population, and the standard deviation around that mean is 10 points. A higher score reflects higher levels of physical, mental, and social health.
Magnitude of change in PROMIS Physical Function scaleBaseline, 6 week, 12 weekPatient-Reported Outcomes Measurement Information System (PROMIS) Physical Function Computer Adaptive Test (CAT). PROMIS Physical Function instruments measure self-reported capability rather than actual performance of physical activities. This includes the functioning of one's upper extremities (dexterity), lower extremities (walking or mobility), and central regions (neck, back), as well as instrumental activities of daily living, such as running errands. With CAT, participant responses guide the system's choice of subsequent items from the full item bank (165 items in total) and a T-Score is generated. T-Score distributions are standardized such that a 50 represents the average (mean) for the US general population, and the standard deviation around that mean is 10 points. A higher score reflects higher levels of physical functioning.

Outcome results

None listed

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