Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
ID04630496

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

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 65 years or older
  • Preparing to undergo thoracic surgery at Brigham and Women's Hospital (BWH)
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Pre-Operative Exercise Tracking

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

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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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