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The validity of performance tests, the 4 meter gait speed and the 5 repetitions sit to stand test, in patients suffering PF in daily clinical practice

The validity of performance tests, the 4 meter gait speed and the 5 repetitions sit to stand test, in patients suffering PF in daily clinical practice - Performance tests in pulmonary fibrosis: PT-PF

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42289
Enrollment
80
Registered
2015-04-24
Start date
2015-05-21
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

lung fibrosis Pulmonary fibrosis

Interventions

Pulmonary Fibrosis
Clinimetric research
Exercise

Sponsors

Sint Antonius Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Patients with PF, visiting outpatient respiratory clinic at St Antonius Hospital in Nieuwegein (Expertise Centre Interstitial Lung disease, cIL) for routine medical control

Exclusion criteria

Exclusion criteria: Absolute contraindications Acute myocardial infarction (3-5 days); Unstable angina; Uncontrolled arrhythmias causing symptoms or haemodynamic compromise; Syncope; Active endocarditis; Acute myocarditis or pericarditis; Symptomatic severe aortic stenosis; Uncontrolled heart failure; Acute pulmonary embolus or pulmonary infarction; Thrombosis of lower extremities; Suspected dissecting aneurysm; Uncontrolled asthma; Pulmonary oedema; Acute respiratory failure; Acute noncardiopulmonary disorder that may affect exercise performance or be aggravated by exercise (i.e. infection, renal failure, thyrotoxicosis); Mental impairment leading to inability to cooperate;A subject that meets any of the following criteria, will be in- or excluded by the judge of the pulmonologist:;Relative contraindications Room air SpO2 at rest 85% (arterial oxygen saturation measured by pulse oximetry); Left main coronary stenosis or its equivalent; Moderate stenotic valvular heart disease; Severe untreated arterial hypertension at rest (200 mmHg systolic, 120 mmHg diastolic); Tachyarrhythmias or bradyarrhythmias; High-degree atrioventricular block; Hypertrophic cardiomyopathy; Significant pulmonary hypertension; Advanced or complicated pregnancy; Electrolyte abnormalities; Orthopaedic impairment that prevents walking

Design outcomes

Primary

MeasureTime frame
The main study parameters are: 4MGS - the maximum gait speed in meters per second (m/sec). 5STS - the shortest time (seconds) required to stand five times from sitting in a chair. 6WMT - the maximum walking distance (meters).

Secondary

MeasureTime frame
• SF-36 (IPF): 8 dimensions of Health-related quality of life. • MRC: a self administered questionnaire about perceived breathlessness. • Self efficacy: self reported activity limitation • Borg dyspnoe and Borg fatigue • Pulmonary function, baseline pulmonary test results: FVC, FEV1, DLCO • Oxygen saturation • Blood pressure (systolic/diastolic). • Body Mass Index (height / weight*weight). • Lean Body Mass (subtracting body fat weight from total body weight). • Grip strength (Jamar dynamometer). • Feasibility of performance tests (Likert scale), patient experience. • Utility of performance tests (Likert scale), assessor experience.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)