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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04667065
Acronym
PREPACHIR
Enrollment
29
Registered
2020-12-14
Start date
2021-03-01
Completion date
2023-01-01
Last updated
2023-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

smartwatch, lung cancer operation, physical exercices

Brief summary

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.

Interventions

OTHERPhysical activity

Physical activity with the remotely guidance of physical activity teachers

Sponsors

Centre Hospitalier Intercommunal Creteil
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

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

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Measure of VO2 max .1 day before surgerycomparison of VO2 max at inclusion and one day before surgery

Secondary

MeasureTime frame
maximum distance covered in the 6-minute walking tone day before surgery
post-surgery complicationsAt 1 month and 3 months
number of individuals who participated in the physical activity programone day before surgery
post surgery intubation durationAt 1 month
Number of patients who used the remotely guided physical preparationone day before surgery
number of days with oxygenAt 1 month and 3 months
(forced expiratory volumeAt 1 month and 3 months
capacity of carbon monoxideAt 1 month and 3 months
number of days at hospitalAt 3 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026