Development & Validation of Preoperative Objective Physiological Evaluation
ConditionCardiorespiratory Fitness
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorDuke University
About this trial
This study will compare the measured oxygen consumption (VO2) obtained during sub-maximal exercise testing with the estimated VO2 derived from a non-exercise questionnaire.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age 18 and older
Able to speak English
Ambulatory [assistive devices ok]
Preoperative Anesthesia and Surgical Screening (PASS) clinic patient with DASI score <34
Disqualifiers
Acute myocardial infarction (3-5 days)
Unstable angina
Severe untreated arterial hypertension at rest (>200 mm Hg systolic, >120 mm Hg diastolic)
Resting heart rate > 120 bpm
Trial design
Design model
Crossover
Treatments tested in this trial
Exercise
BehavioralCalculate oxygen consumption
Treatment groups
100 Participants
are divided into 2 treatment groupsGroup A: 6MST VO2Active comparator 1 intervention
Group B: DASI VO2Active comparator 1 intervention
Trial outcomes
Primary outcomes
1
Total amount of oxygen consumed per minute
Oxygen consumption measured in mL/min
Time frame
Up to 15 minutesSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov