Geriatric Thoracic Surgery Ambulation Challenge

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65+
SponsorDana-Farber Cancer Institute

About this trial

This study is examining collecting data on steps walked (ambulation) per day by thoracic surgery patients over the age of 65 years-old before surgery.

The name(s) of the study device involved in this study is:

* Fitbit inspire

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients Aged ≥ 65 years

Who are preparing to undergo thoracic surgery at Brigham and Women's Hospital (BWH)

Disqualifiers

Patients who are completely non-ambulatory (i.e. wheelchair-bound-patients) *

Those who lack capacity to consent due to cognitive disease.

Patient for which surgery is felt to be more urgent and therefore performed earlier then our required timeframe for intervention.

Patients with cardiac disease or angina for which formal cardiac testing is required for clearance.

Trial design

Design model

Single group

Treatments tested in this trial

  • Fitbit

    Behavioral

    Electronic activity tracker

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: PRE-OPERATIVE EXERCISE TRACKINGExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Step Tracking Rate

Feasibility will be determined by the successful tracking of steps and keeping a diary of step-count for one-week duration. Completion of a minimum of 5/7 days will be considered as a success

Time frame
1 week
2

Diary of Steps Rate

Feasibility will be determined by the successful tracking of steps and keeping a diary of step-count for one-week duration. We will consider completion of a minimum of 5/7 days as a success.

Time frame
1 week
3

Return Rate

If 90% of trackers are returned, it will be considered a successful return.

Time frame
1 week
4

Data Retrieval Rate

assess extraction of the data from the mobility upon return. Success will be considered if 90% of data is retrievable

Time frame
1 week

Secondary outcomes

Other outcomes

Sponsors and contacts

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