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Ergometer Training in Patients With OSA

Telemedizinisches Trainings-Monitoring Von Patienten Mit Obstruktivem Schlafapnoesyndrom

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01457729
Enrollment
24
Registered
2011-10-24
Start date
2011-02-28
Completion date
2011-12-31
Last updated
2012-09-18

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

Conditions

Obstructive Sleep Apnea

Keywords

ergometer, training, motivation, telemonitoring, sleep apnea

Brief summary

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.

Interventions

BEHAVIORALMotivation by Telephone Call

Telephone call not exceeding 10 minutes according to a protocol

Sponsors

Institut für Pneumologie Hagen Ambrock eV
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Suspected OSA 2. Capable of giving consent

Exclusion criteria

1. Symptomatic cardial infarction 2. Decompensated cardiac insufficiency 3. Hemodynamically effective cardiac arrhythmias 4. Hemodynamically significant Vitia (heart disease) 5. Insufficiently regulated arterial hypertension 6. Global respiratory insufficiency 7. Significant partial insufficiency (PAO2 \<50mmHg or SaO2 \< 80% at rest) 8. State after decompensation of Cor Pulmonale 9. Right ventricular strain at pulmonary hypertension at rest (pulmonary arterial pressure \> 20 mmHg) 10. Severe osteoporosis 11. Higher degree of lung functional restriction: FEV1 \<50% oder \>60% of nominal value after bronchospasmolysis 12. Working performance on ergometer \< 50% 13. Unstable bronchial asthma 14. Exacerbated COPD 15. Heavily overweight (BMI \>40 or weight \>140kg)

Design outcomes

Primary

MeasureTime frame
Training time4 weeks

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026