Clinical trial · Interventional
Evaluation of a Remotely Guided Physical Preparation by a Physical Activity Teacher Adapted With the Help of a Smartwatch Before Bronchial Cancer Surgery
NCT04667065CI-TRIAL-00066595PREPACHIRcompletedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lung Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Physical activity | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- OTHER
- label
- Physical activity with smartwatch before bronchial cancer surgery
- interventionNames
- Other: Physical activity
Primary outcomes (1)
- measure
- Measure of VO2 max .
- timeFrame
- 1 day before surgery
- description
- comparison of VO2 max at inclusion and one day before surgery
Secondary outcomes (9)
- measure
- Number of patients who used the remotely guided physical preparation
- timeFrame
- one day before surgery
- measure
- maximum distance covered in the 6-minute walking t
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.