Cardiovascular Disease Clinical Trial
Official title:
Effect of Intermittent Hypoxia Therapy on Functional Capacity in Geriatric Cardiac Patients With Functional Impairment During a Cardiac Rehabilitation Program: a Pilot Study
Verified date | July 2019 |
Source | Istituti Clinici Scientifici Maugeri SpA |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a randomized control pilot study to assess the effect of intermittent hypoxia therapy on functional capacity vs conventional care in old patients with functional impairment admitted to a Phase 2 in-hospital cardiac rehabilitation program.
Status | Completed |
Enrollment | 30 |
Est. completion date | October 30, 2020 |
Est. primary completion date | June 30, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 75 Years and older |
Eligibility | Inclusion Criteria: - Admission to a Phase 2 in-hospital cardiac rehabilitation program because of a recent index event; - Provision of signed and dated informed consent form; - Age = 75 years; - Basic venous blood oxygen saturation (SpO2) level > 93% measured at the fingertip; - SPPB score < 7; - New York Heart Association (NYHA) Class I-III. Exclusion Criteria: - Inability to give informed consent (diminished understanding or comprehension); - Age < 75 years; - SPPB Score = 7; - NYHA Class IV and/or concomitant i.v. therapy with cardiovascular active drugs; - Uncontrolled angina pectoris; - Uncontrolled arterial hypertension; - Uncontrolled atrial or ventricular arrhythmias; - Active pericarditis or myocarditis; - Need of continuous or intermittent O2 therapy; - Hb < 10 g/dl; - Severe concomitant non-cardiac diseases such as cancer or any other systemic disease limiting to participate in the study - Acute inflammatory diseases; - Acute non-cardiac somatic diseases, or somatic diseases with symptoms of decompensation; - Currently implanted left ventricular assist device; - Inability to accept the procedure of breathing via facial mask. |
Country | Name | City | State |
---|---|---|---|
Italy | Istituti Clinici Scientifici Maugeri IRCCS | Pavia |
Lead Sponsor | Collaborator |
---|---|
Istituti Clinici Scientifici Maugeri SpA |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in SPPB score | The Short Physical Performance Battery (SPPB) is a series of physical performance tests used in older persons to assess lower extremity function and mobility.
Score total: minimum 0 (lowest performance), maximum 12 (highest performance). Three subscales (minimum 0, maximum 4 points each one): balance test, gait speed test, chair stand test. |
30 days | |
Secondary | Changes in distance at the 6-min walking test | 6-min walking test is a test for functional evaluation based on walking distance performed by the patient in the time window at the individual walking speed. Score in meters: minimum zero, maximum indefinite | 30 days | |
Secondary | Changes in peak exercise oxygen uptake (peak VO2) | Peak VO2 represents the maximal individualized oxygen consumption at the peak effort, evaluated by means of cardiopulmonary exercise testing, expressed by means of ml of oxygen per Kg of body weight per minute. | 30 days | |
Secondary | Changes in basal blood pressure | Expressed by means of mmHg. Indicator of haemodynamic status. | 30 days | |
Secondary | Changes in basal heart rate | Expressed by means of number of beats per minute. Indicator of haemodynamic status. | 30 days | |
Secondary | Changes in EuroQoL score | European Quality of Life score (EuroQoL). Score: from 0 (lowest condition) to 10 (best condition). | 30 days | |
Secondary | Changes in geriatric depression scale | 30 items with relative categorization (1 present; 0 absent). Minimum 0 points (absence of depression), maximum 30 point (highest grade of depression). | 30 days | |
Secondary | Changes in minimental state evaluation | Tool for evaluation of cognitive status in older patients. Minimum score 0 (absence of cognitive impairment), maximum 30 (highest grade of cognitive impairment) | 30 days |
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