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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04034082
Other study ID # 2233CE
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 12, 2019
Est. completion date October 30, 2020

Study information

Verified date July 2019
Source Istituti Clinici Scientifici Maugeri SpA
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Because the improvement of exercise tolerance reduces mortality in elderly patients affected by cardiovascular disease, intermittent hypoxia therapy (IHT) - defined as repeated episodes of hypoxia interspersed with normoxic periods delivered by an ad hoc device - might be a valuable tool to be associated to structured cardiac rehabilitation (CR) interventions. The present study is a pilot, monocentric, randomized (randomization ratio 1:1), parallel group study to assess the effect of IHT on functional capacity vs conventional care in old patients with functional impairment admitted to a phase 2 in-hospital cardiac rehabilitation program. The study will enroll cardiac patients of both genders, ≥ 75 years and with a functional impairment assessed by a Short Physical Performance Battery (SPPB) score < 7. The effect of IHT on functional capacity will be evaluated on top of the conventional multidisciplinary CR intervention, by means of SPPB score variation; variations in quality of life and cognitive status will also be evaluated as secondary goals of the study. The total amount of IHT sessions per patient will be 10, 1 per day over 2 weeks, the duration of each single procedure will be 45 min and the Hypoxic O2 conc.% will be 14-10. The study was approved by local ethic committee.


Recruitment information / eligibility

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.

Study Design


Intervention

Device:
Intermittent hypoxia therapy
Intermittent Hypoxic Therapy (further referred to as IHT). A typical IHT session consists of repeated short-term moderate hypoxia (down to 10 vol.% O2), interrupted by brief periods of reoxygenation. These periods of recovery could be either normoxic (21 vol.% O2, Hypoxia-Normoxia mode) or hyperoxic (30-35 vol.% O2, Hypoxia-Hyperoxia mode, further referred to as IHHT). The gas mixtures are supplied to a patient via facial mask.
Other:
Conventional phase 2 cardiac rehabilitation programme
The core components of a Phase 2 in-hospital cardiac rehabilitation program include: 1) patient assessment with medical control to promote clinical stabilization and optimization of pharmacologic treatment; 2) physical activity counselling; 3) prescription of an individualized exercise training; 4) diet/nutritional counselling; 5) weight control management; 6) Lipid management; 7) blood pressure monitoring and management; 8) smoking cessation; 9) vocational support; 10) psychosocial management..

Locations

Country Name City State
Italy Istituti Clinici Scientifici Maugeri IRCCS Pavia

Sponsors (1)

Lead Sponsor Collaborator
Istituti Clinici Scientifici Maugeri SpA

Country where clinical trial is conducted

Italy, 

Outcome

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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