Evaluation of a Remotely Guided Physical Preparation by a Physical Activity Teacher Adapted With the Help of a Smartwatch Before Bronchial Cancer Surgery

NCT ID: NCT04667065

Last Updated: 2023-05-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

29 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-01

Study Completion Date

2023-01-01

Brief Summary

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This is a study of a preoperative rehabilitation program with remotely guided high-intensity exercises by physical activity teachers adapted to a smartwatch in patients with operable lung cancer.

Detailed Description

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Conditions

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Lung Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Patient with non-small cell bronchial cancer with indication of curative surgical resection.
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Physical activity with smartwatch before bronchial cancer surgery

Group Type OTHER

Physical activity

Intervention Type OTHER

Physical activity with the remotely guidance of physical activity teachers

Interventions

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Physical activity

Physical activity with the remotely guidance of physical activity teachers

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Major patient, age ≥ 18
* Patient with non-small cell operable bronchial cancer without indication of neo-adjuvant chemotherapy
* Affiliated with a social security plan
* VEMS \< 80% and/or DLCO\<80%
* High-intensity training achievable for at least 10 days before surgery
* Acceptant to participate in the protocol
* Ability to follow the STIMUL program of education focused on adapted physical activity
* Have a smartphone that can download the mobile app
* have the ability to understand, read and write French

Exclusion Criteria

* Patient unable to consent: under guardianship or curatorship
* Patient refusing surgery
* Non-operable patient due to comorbidities or unseable tumour
* Poor understanding of the smartwatch
* Severe cognitive or psychiatric disorders
* Pregnancy in progress
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Intercommunal Creteil

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Centre hospitalier intercommunal de Créteil

Créteil, , France

Site Status

Countries

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France

Other Identifiers

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PREPACHIR

Identifier Type: -

Identifier Source: org_study_id

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