Physical Activity Measure Application (MARCHE)

Hopital Foch

Status: Completed

Conditions: Physical Inactivity; Post-Surgical Complication

Treatments: Device: Physical activity measure

Study type: Interventional

Funder types: Other

Identifiers

NCT06492161

2020_0140

Details and patient eligibility

About

Although there is a strong physiological rationale for the benefit of post-operative mobilization, the evidence supporting these effects in surgical cohorts is conflicting, and there is a lack of research to guide the clinical implementation of early mobilization protocols. There is also a need to better evaluate the physical activity performed by physical activity tients outside the supervised mobilization protocol, to better understand its potential benefits on post-operative recovery. In adition, the objective measurement of physical activity has several advantages over declarative measures.

Full description

Prolonged immobilization after surgery is known to have detrimental effects. Although postoperative recommendations favor early mobilization, the lack of quantification of physical activity poses a problem for the implementation of early mobilization protocols..

An application named "ACTIM" has been developed with the aim of automating the personalized assessment of postoperative physical activity. The healthcare team (nurses or physiotherapists...), will share the information with the patient and will complete the assessment using personalized physical activity objectives for the day.

The purpose of this study is to assess this application in real-life settings to provide patients with information on their physical activity after lung resection by thoracoscopy or robotic surgery. This assessment will serve as a reference for future studies.

Enrollment: 28 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient 18 years of age or older
• Scheduled for thoracoscopic or robotic lung resection
• Agreeing to wear an ActiGraph GT3X accelerometer from 4 days post-surgery
• Having signed a consent form
• Affiliated with a health insurance

Exclusion criteria

• Pregnant or breastfeeding woman
• Patient unable to move independently (paraplegic, etc.)
• Patient deprived of liberty or under guardianship

Trial design

Primary purpose: Prevention

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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28 participants in 1 patient group

GT3X ActiGraph's activity monitor

Experimental group

Description:

Patients who have undergone thoracic surgery wearing an ActiGraph GT3X-BT device that measures and records physical movement associated with daily activity.

Treatment:

Device: Physical activity measure