Status
Conditions
Treatments
About
Goal of this study is to evaluate management with high intensity re-entrainment during the postoperative hospital phase.
This type of early treatment with as little intervention time has so far never been done. The investigators therefore want to carry out this feasibility study in order to collect the data needed to calculate the number of randomized control trial. Investigators will also evaluate the feasibility of this project concerning recruitment, intervention in the hospital phase and data collection once the return home. The evaluation of the activity will be done one month after the return to home by means of a actigraphy of one week.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
30 participants in 2 patient groups
Loading...
Central trial contact
Olivier Contal, phD; Mélissa Lecocq, MscStudent
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal