Skip to main content
OpenTrials
Completed

NCT Number: NCT04667065

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Lung Cancer Lung Diseases Lung Neoplasms Neoplasms Neoplasms by Site Respiratory Tract Diseases Respiratory Tract Neoplasms Thoracic Neoplasms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre hospitalier intercommunal de Créteil

Créteil, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Physical activity

Other

Physical activity with the remotely guidance of physical activity teachers

Primary outcomes

  1. Measure of VO2 max .

    Time frame: 1 day before surgery

    comparison of VO2 max at inclusion and one day before surgery

Secondary outcomes

  1. Number of patients who used the remotely guided physical preparation

    Time frame: one day before surgery

  2. maximum distance covered in the 6-minute walking t

    Time frame: one day before surgery

  3. post-surgery complications

    Time frame: At 1 month and 3 months

  4. number of individuals who participated in the physical activity program

    Time frame: one day before surgery

  5. post surgery intubation duration

    Time frame: At 1 month

  6. number of days at hospital

    Time frame: At 3 months

  7. number of days with oxygen

    Time frame: At 1 month and 3 months

  8. (forced expiratory volume

    Time frame: At 1 month and 3 months

  9. capacity of carbon monoxide

    Time frame: At 1 month and 3 months

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Intercommunal Creteil

Other

Registry information

Acronym: PREPACHIR

Important dates

Study start
2021
Primary completion
2021
Study completion
2023
First posted
Dec 14, 2020
Registry last updated
May 23, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.