Ergometer Training in Patients With OSA

Patients with suspected OSA (obstructive sleep apnoea syndrome) are asked to use a standard bike ergometer which is additionally equipped with a system to gather training data and the ability to send daily training time to an internet server to which the physician has access. Training time of two groups is compared. Group one is not motivated while group two benefits from telephone feedback when training time declines. It is presumed that training time increases with better information and response to training behaviour.

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Key information

Conditions

Obstructive Sleep Apnea Apnea Dyssomnias Nervous System Diseases Respiration Disorders Respiratory Tract Diseases Sleep Apnea Syndromes Sleep Apnea, Obstructive Sleep Disorders, Intrinsic Sleep Wake Disorders

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Helios Klinik Hagen Ambrock

Hagen, North Rhine-Westphalia, 58091, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Suspected OSA
Capable of giving consent

Exclusion criteria

Symptomatic cardial infarction
Decompensated cardiac insufficiency
Hemodynamically effective cardiac arrhythmias
Hemodynamically significant Vitia (heart disease)
Insufficiently regulated arterial hypertension
Global respiratory insufficiency
Significant partial insufficiency (PAO2 <50mmHg or SaO2 < 80% at rest)
State after decompensation of Cor Pulmonale
Right ventricular strain at pulmonary hypertension at rest (pulmonary arterial pressure > 20 mmHg)
Severe osteoporosis
Higher degree of lung functional restriction: FEV1 <50% oder >60% of nominal value after bronchospasmolysis
Working performance on ergometer < 50%
Unstable bronchial asthma
Exacerbated COPD
Heavily overweight (BMI >40 or weight >140kg)

Treatment and study plan

Motivation by Telephone Call

Behavioral

Telephone call not exceeding 10 minutes according to a protocol

Primary outcomes

Training time

Time frame: 4 weeks

Sponsors and collaborators

Lead sponsor

Institut für Pneumologie Hagen Ambrock eV

Industry

Registry information

Official study title

Telemedizinisches Trainings-Monitoring Von Patienten Mit Obstruktivem Schlafapnoesyndrom

Important dates

Study start: 2011
Primary completion: 2011
Study completion: 2011
First posted: Oct 24, 2011
Registry last updated: Sep 18, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed