NCT04583176

Completed

Measurement of Physical Activity in the First Days After Tho...

Hopital Foch Source

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Other study identifiers

Sponsor study identifier

2020_0046

Study Type

observational

Actual enrollment (reported)

60

Locations

1 country

Sites

1

Timeline

Study Start

November 16, 2020

Actual (reported)

Primary Completion

July 13, 2021

Actual (reported)

Study Completion

July 13, 2021

Actual (reported)

Brief Summary

Objective measurement of physical activity has several advantages compared to declarative measures: exemption from memory bias and desirability bias, more precise evaluation, taken into account activities of low intensity, measurement of physical activity and sedentariness profiles (number and duration of periods of activity, number of breaks in sedentary lifestyles). The aim of this study is to assess the early postoperative mobility of patients who have undergone pulmonary excision by thoracoscopy or robot surgery using ActiGraph GT3X accelerometer. This assessment will serve as a reference element for further studies.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 60 participants
Study completion date: July 13, 2021
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
October 5, 2020
Actual (reported)
First Posted
October 12, 2020
Actual (reported)
Study Start
November 16, 2020
Actual (reported)
Primary Completion
July 13, 2021
Actual (reported)
Study Completion
July 13, 2021
Actual (reported)

Last Updated: January 19, 2022
Status Verified: January 2022
Last Update Submitted: January 18, 2022

Conditions

Pulmonary Disease

Keywords

ActiGraph GT3XPhysical activity

Outcome Measures

Primary Outcomes (1)

Measurement of postoperative mobility during the first postoperative days
Number of steps
Day 5

Secondary Outcomes (11)

Volume of physical activity assessed by accelerometry during the first postoperative days
Day 5
Overall intensity of physical activity assessed by accelerometry during the first postoperative days
Day 5
Duration and intensity of physical activity assessed by accelerometry during the first postoperative days
Day 5
Sedentary time assessed by accelerometry during the first postoperative days
Day 5
Best natural effort assessed by accelerometry during the first postoperative days
Day 5
+6 more secondary outcomes

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

Patients having to undergo pulmonary excision by thoracoscopy or robotic surgery.

You may qualify if:

Age ≥ 18 years

Sponsors & Collaborators

Hopital Foch
Otherlead

Study Sites (1)

Hôpital Foch

Suresnes, 92150, France

MeSH Terms

Conditions

Lung DiseasesMotor Activity

Condition Hierarchy (Ancestors)

Respiratory Tract DiseasesBehavior

Study Officials

Julien FESSLER, MD
Foch Hospital
PRINCIPAL INVESTIGATOR
Marc FISCHLER, PhD
Foch Hospital
STUDY CHAIR

Enrollment

60 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

October 5, 2020

First Posted

October 12, 2020

Study Start

November 16, 2020

Actual (reported)

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Having to undergo pulmonary excision by thoracoscopy or robotic surgery

Accepting to wear a belt fitted with an ActiGraph GT3X accelerometer for a maximum of 5 days post surgery

Affiliated to a Health Insurance plan

Having given an oral non-opposition

You may not qualify if:

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

Contact the study team to confirm eligibility.

Primary Completion

July 13, 2021

Actual (reported)

Study Completion

July 13, 2021

Actual (reported)

Last Updated

January 19, 2022

Record last verified: 2022-01

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT04583176
Data provider: ClinicalTrials.gov
Source updated: 2022-01-19
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:38:34 UTC

Locations

FR(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (11)

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations