Ambulation to Improve Recovery With Wearable TECHnology (AIRTECH) Study
Sponsor: M.D. Anderson Cancer Center
Trial Details
| Condition | Lung Carcinoma |
| Intervention | Best Practice; Health Promotion and Education; Medical Device Usage and Evaluation; Quality-of-Life Assessment; Questionnaire Administration |
| Phase | NA |
| Status | Recruiting |
| Participants | 240 |
| Est. Completion | 2 Feb 2027 |
| Last Updated | 16 Apr 2026 |
Primary Outcome
Clavien-Dindo postoperative morbidity (POM) score
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * 18 years or older * English speaking * Ambulatory preoperatively * Patients undergoing at least a lobectomy * Must own a smart phone and be willing to install the Fitbit application (App) * Adequate internet connection via wifi or wireless network connection with smartphone * Patients who are not already using a wearable device to track daily steps Exclusion Criteria: * Medical, psychiatric, cognitive or other conditions that compromise the patient's ability to understand the patient information, to give informed consent, to comply with the study protocol or to complete the study. * Cannot maintain activity monitor in place at the time of consent * Pregnant patients
Trial Sites
Countries
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