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Clinical Trials/NCT01625819
NCT01625819CompletedNot Applicable

Exploring Tai Chi as a Behavioral Intervention for Heart Failure Patients

University of California, San Diego1 site in 1 country135 target enrollmentStarted: August 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
135
Locations
1
Primary Endpoint
End Systolic Volume (ESV)

Study Overview

Brief Summary

The objective of this research is to compare Tai Chi versus Resistance Exercise, Health Education and usual care for changes in cardiac functional capacity measured for ability of the heart to pump by measuring ejection fraction (EF), end systolic and diastolic volumes in heart failure (HF) patients. Also measured will be changes in physical function measured by walking speed and distance in the 6-min walk task, work performed during a bicycle task, and changes in daily physical activity. The investigators will compare groups for altered well-being including: depression, sleep disturbances, fatigue, mindfulness, spirituality and quality of life. In addition the investigators will compare groups for altered vascular and pro-inflammatory markers, catecholamines, and autonomic function at rest and in response to the bicycle task. Also, the investigators will assess cardiac related hospitalization and death over a 12 month period by examining medical records.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Ability to perform a 6-minute walk task, with or without use of a cane or walker (must use the same walking assistance device during each session), and walk under 500 meters during task.
  • •Symptoms of chronic heart failure for at least 3 months.
  • •Clinically stable- defined as not having been hospitalized for a 3 month period, on stable doses of neurohormonal blocking agents and diuretics for at least 3 months.
  • •ACC/AHA stages B and C
  • •Ability to perform light to moderate exercise (NYHA functional class II and III)
  • •Presence of HF with an ejection fraction less than 40%, or diastolic dysfunction
  • •Ability to give informed consent
  • •At least18 years of age

Exclusion Criteria

  • •History of recent myocardial infarction (1 month)
  • •Angina not adequately managed with nitrates.
  • •Aortic or mitral stenosis
  • •Coronary revascularization, mitral valve repair or any other cardiac surgery or implantation of a biventricular pacemaker within the past 6 months.
  • •Severe COPD
  • •Recent stroke or significant cerebral neurologic impairment.
  • •Active Suicidality
  • •Currently participating in an exercise program.
  • •Currently taking mood stabilizers (e.g. lithium), benzodiazepines or antipsychotics.
  • •Medications (steroids) and medical conditions affecting immune status not limited to Grave's Disease, Rheumatoid Arthritis, Hashimoto's Disease, Sjogren's Disease, Lupus, Multiple Sclerosis

Arms & Interventions

Tai Chi

Experimental

32 1-hour group sessions of Tai Chi instruction

Intervention: Tai Chi (Behavioral)

Resistance Band

Active Comparator

32 1-hour bi-weekly group sessions of Resistance Band exercises

Intervention: Resistance Band (Behavioral)

Health Education

Placebo Comparator

32 1-hour bi-weekly group sessions of health education

Intervention: Health Education (Behavioral)

Care as Usual

No Intervention

Receive usual cardiology care for 4 months between pre- and post-treatment testing

Outcomes

Primary Outcomes

End Systolic Volume (ESV)

Time Frame: Change from Baseline in ESV Immediately Following 16 Weeks of Treatment

Determine whether Tai Chi compared with Resistance Exercise and Health Education control condition will lead to a greater improvement in cardiac functional capacity as measured by ESV on echocardiogram.

Left Ventricular Ejection Fraction (%LVEF)

Time Frame: Change from Baseline in %LVEF Immediately Following 16 Weeks of Treatment

Determine whether Tai Chi compared with Resistance Exercise and Health Education control condition will lead to a greater improvement in cardiac functional capacity as measured by %LVEF on echocardiogram.

End Diastolic Volume (EDV)

Time Frame: Change from Baseline in EDV Immediately Following 16 Weeks of Treatment

Determine whether Tai Chi compared with Resistance Exercise and Health Education control condition will lead to a greater improvement in cardiac functional capacity as measured by EDV on echocardiogram.

Secondary Outcomes

  • Beck Depression Inventory (BDI) at Post-Treatment(Change from Baseline in BDI Scores Immediately Following 16 Weeks of Treatment)
  • Minnesota Living with Heart Failure Questionnaire (MLHFQ) at Post-Treatment(Change from Baseline in MLHFQ Scores Immediately Following 16 Weeks of Treatment)
  • B-type Natriuretic Peptide (BNP)(Change from Baseline in BNP Immediately Following 16 Weeks of Treatment)
  • Average Number of Steps Across 3 Days (Steps)(Change from Baseline in Steps Immediately Following 16 Weeks of Treatment)
  • MFSI at 1-Year Follow-Up(Change From Baseline in MFSI Scores at the 1-Year Follow-Up Assessment)
  • MHLFQ at 8-Week Follow-Up(Change from Baseline in MHLFQ at 8-Week Follow-Up Assessment)
  • Six-Minute Walk Task (6MWT)(Change from Baseline in 6MWT Immediately Following 16 Weeks of Treatment)
  • Work Performed on Bicycle Ergometer Task (Watts)(Change from Baseline in Watts Immediately Following 16 Weeks of Treatment)
  • PSQI at 8-Week Follow-Up(Change from Baseline in PSQI scores at 8-week follow-up)
  • MFSI at 8-Week Follow-Up(Change From Baseline in MFSI Scores at 8-week Follow-up Assessment)
  • Pittsburgh Sleep Quality Inventory (PSQI) at Post-Treatment(Change from Baseline on the (PSQI) Immediately Following 16 Weeks of Treatment)
  • BDI at 8-Week Follow-Up(Change from Baseline in BDI scores at 8-week follow-up)
  • BDI at 1-Year Follow-Up(Change from Baseline in BDI Scores at 1-year follow-up)
  • PSQI at 1-Year Follow-Up(Change from Baseline in PSQI Scores at 1-year Follow-Up Assessment)
  • Multidimensional Fatigue Symptom Inventory (MFSI) at Post-Treatment(Change from Baseline in MFSI Scores Immediately Following 16 Weeks of Treatment)
  • MHLFQ at 1-Year Follow-Up Assessment(Change from Baseline in MHLFQ Scores at 1-year Follow-Up Assessment)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Laura S. Redwine, PhD

Assistant Adjunct Professor

University of California, San Diego

Study Sites (1)

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