Actively Recruiting
Pre-Operative Exercise Challenge in Geriatric Thoracic Patients
Led by Dana-Farber Cancer Institute · Updated on 2025-04-13
30
Participants Needed
2
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying thoracic surgery patients aged 65 and older to collect data on the number of steps they walk each day before surgery. The goal is to see if patients can wear a wrist step-tracker and keep a daily step log for one week, which will help in future studies where step-goals may be set to measure pre-surgery activity accurately. This study is a feasibility study to assess the willingness of patients to track their steps using technology. Participants will be given a Fitbit Inspire device to wear on their wrist for one week prior to their scheduled surgery. They will be instructed on how to use the device and asked to keep a daily log of their steps. During this week, the study team will call participants once to check on their progress. After the week, participants will return the Fitbit and their step log at a pre-surgery clinic visit or on the day of surgery, whichever comes first. During the study, baseline information will be collected from participants' electronic medical records. Researchers will measure outcomes such as the rate of step tracking, diary completion, return of the device and log, and data retrieval over the one-week period. The total participation time involves one week of wearing the tracker before surgery, with follow-up during the week and device return at or before surgery. About 30 people are expected to participate in this research conducted by the Dana-Farber Cancer Institute.
CONDITIONS
Brief Title
Geriatric Thoracic Surgery Ambulation Challenge
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 65 years or older
- Preparing to undergo thoracic surgery at Brigham and Women's Hospital (BWH)
You will not qualify if you...
- Patients who are completely non-ambulatory (wheelchair-bound)
- Patients lacking capacity to consent due to cognitive disease
- Patients requiring urgent surgery earlier than the study timeframe
- Patients with cardiac disease or angina requiring formal cardiac testing for clearance
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 week
Participants are provided a Fitbit to wear for tracking steps and keep a daily log for 1 week prior to their scheduled surgery. They receive one check-in call during this period.
1 week of step tracking with 1 progress check-in call
Trial Site Locations
Total: 2 locations
1
Brigham and Women's Hospital
Boston, Massachusetts, United States, 02115
Actively Recruiting
2
Dana-Farber Cancer Institute
Boston, Massachusetts, United States, 02215
Actively Recruiting
Research Team
M
Michael T Jaklitsch, MD
A
Anupama Singh, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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