RECRUITING

Development & Validation of Preoperative Objective Physiological Evaluation

Conditions

Cardiorespiratory Fitness areobic power cardiopulmonary exercise testing exercise capacity functional capacity physical activity

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Development & Validation of Preoperative Objective Physiological Evaluation

Quick Facts

Study Start:2021-11-23

Study Completion:2026-01-01

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05092126

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Age 18 and older * Able to speak English * Ambulatory \[assistive devices ok\] * Preoperative Anesthesia and Surgical Screening (PASS) clinic patient with DASI score \<34 * Able to provide informed consent	* 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 * Room air desaturation at rest on room air \<85% * Inmate of correctional facility (i.e. prisoner) * Diagnosed history of dementia * Inability to ambulate independently * Considered inappropriate to participate by Principal Investigator

Inclusion Criteria

Exclusion Criteria

* Age 18 and older
* Able to speak English
* Ambulatory \[assistive devices ok\]
* Preoperative Anesthesia and Surgical Screening (PASS) clinic patient with DASI score \<34
* Able to provide informed consent

* 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
* Room air desaturation at rest on room air \<85%
* Inmate of correctional facility (i.e. prisoner)
* Diagnosed history of dementia
* Inability to ambulate independently
* Considered inappropriate to participate by Principal Investigator

Contacts and Locations

Study Contact

David MacLeod, FRCA

CONTACT

919-812-3201

david.macleod@duke.edu

Ashley Burke, BS

CONTACT

Principal Investigator

David MacLeod, FRCA

PRINCIPAL_INVESTIGATOR

Duke University

Study Locations (Sites)

Duke University Health System

Durham, North Carolina, 27710

United States

Collaborators and Investigators

Sponsor: Duke University

David MacLeod, FRCA, PRINCIPAL_INVESTIGATOR, Duke University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-11-23

Study Completion Date2026-01-01

Study Record Updates

Study Start Date2021-11-23

Study Completion Date2026-01-01

Terms related to this study

Keywords Provided by Researchers

areobic power
cardiopulmonary exercise testing
exercise capacity
functional capacity
physical activity

Additional Relevant MeSH Terms

Cardiorespiratory Fitness