Viewing Study NCT03615157


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Study NCT ID: NCT03615157
Status: UNKNOWN
Last Update Posted: 2018-08-03
First Post: 2018-07-30
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Effects of a Home-based Exercise Program on Functional Capacity and Quality of Life in Heart Failure Patients
Sponsor: University of Sao Paulo
Organization:

Study Overview

Official Title: Effects of a Home-based Exercise Program on Functional Capacity and Quality of Life in Heart Failure Patients
Status: UNKNOWN
Status Verified Date: 2018-07
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Heart failure (HF) is a multisystemic disease leading to exercise intolerance and fatigue. Supervised physical training improves functional capacity, quality of life and reduces hospital admissions in HF patients. In this way, home physical training may be a good alternative to patients who, for any reason, cannot perform supervised training. Objective: To asses the effects of a home-based training program on functional capacity, sedentary lifestyle and quality of life of patients with chronic HF compared to supervised training.
Detailed Description: After agreement with the written informed consent, subjects with heart failure (left ventricle ejection fraction bellow or equal 40%) will be included in this study. They will be randomized in two groups: Home-based and Supervised exercise groups. The two groups will be submitted to a twelve-week combined exercise program of aerobic and peripheral muscle training. All volunteers will be assessed at baseline and after twelve weeks of intervention. Peripheric and respiratory muscle strength as well the 6MW analyses were assessed also at 4 and 8 weeks after baseline.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: