Patient Empowerment for Major Surgery Preparation @ Home

NCT04190719 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 225

Last updated 2021-04-30

No results posted yet for this study

Summary

Non-randomized monocentric open cohort study vs historical comparative group testing the efficacy of a multimodal prehabilitation program (based on physical activity, nutritional support and mental preparation) for unfit patients based on nutrition, physical activity and mental preparation in reducing postoperative complications in elective major surgery

Conditions

Interventions

OTHER

multimodal prehabilitation

Paprika prehabilitation program content: patients will have choices for each activity. Messages and motivation will be reinforced by using a mobile app or leaflet advices, according to patient's preferences. * Physical activity promotion by discovering ebike, personalised gymnastics and encouragement to increase the number of daily steps of patients, measured by a wristband and a mobile App * An individualized nutritional optimization plan with dietary advices and protein supplementation (if necessary). * Psychological support will be proposed through auto-hypnosis sensibilisation or management of stress with Cognitive Behavior Stress Management technics

Sponsors & Collaborators

  • EIT Health

    collaborator OTHER
  • Hospital Clinic of Barcelona

    collaborator OTHER
  • Universitätsklinikum Köln

    collaborator OTHER
  • University Clinical Centre, Gdansk

    collaborator OTHER
  • University Hospital, Grenoble

    lead OTHER

Principal Investigators

  • Pierre Albaladejo, Prof. · CHU Grenoble Alpes

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-03
Primary Completion
2021-09-30
Completion
2021-12-31

Countries

  • France

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04190719 on ClinicalTrials.gov