Cardipulmonal Rehabilitation with geriatric patients.
Conditions
Interventions
Group 1: Preparation:
-Consultation of the medical report after accommodation
-decision of participation
-education of the patient and signing of the written consent under supervision of a medical doc
Sponsors
Universität Ulm. Hermann Buhl Institut für Hypoxie- und Schlafmedizinforschung
Eligibility
Sex/Gender
All
Age
65 Years to No maximum
Inclusion criteria
Inclusion criteria: •Age > 65; •Willingness to participate with written consent. •Sufficient peripheral blood flow to deliver a pulseoximetry signal. •Physical and mental capability to perform an Ergospirometry test. (Minimum : 25Watt for 8 minutes) •Minimum Heart Rate and systolic blood pressure adaption of 20% of the resting pulse.
Exclusion criteria
Exclusion criteria: •Final (palliative) status of any disease. •High risk for Cardiac events or Stroke •Cognitive Impairment •Insufficient peripheral blood flow for a reasonable pulseoximetry signal. •Unwillingness to sign the written consent. •Incapability to perform an Ergospirometry test. •Such high dosage of heart and blood circuit medication (ß-Blocker, Amyodaron) that the minimum requirements of adaption to physical stress and hypoxia are not fulfilled. (See above and Pretest) •Patients with a cardiac impairment equivalent to NYHA IV
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The data will be collected at the first day of accomodation in the Hospital via Ergospirometry and Echokardiography. Then each Patient will have to perform 7 trainings each second day. The final test will be after 3 weeks via Ergospirometry and Echokardiography. Main Parameter: Vo2peak | — |
Secondary
| Measure | Time frame |
|---|---|
| Pretest at first day of accomodation: Ecg, Workload, Weight, Bloodpreasure, Vo2 max, oxigensaturation, Puls, Diagnosis Posttest after 3 Weeks: Ecg, Workload, Weight, Bloodpreasure, Vo2 max, oxigensaturation, Puls, Diagnosis | — |
Countries
Germany
Contacts
Public ContactStephan Pramsohler
Universität Ulm. Hermann Buhl Institut für Hypoxie- und Schlafmedizinforschung
Outcome results
None listed