Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Bladder Cancer
  • Postoperative Complications
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Randomised Controlled TrialMasking: Single (Outcomes Assessor)Masking Description: Outcome assessors will not know if patients were allocated to intervention or control groupPrimary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 100 years
Gender
Both males and females

Description

The study is a multicenter randomised controlled trial involving 110 bladder cancer patients screened positive for at least 1 SNAP factor and undergoing neoadjuvant chemotherapy before radical cystectomy. Patients allocated to the intervention group will receive five counselling sessions in 6 weeks ...

The study is a multicenter randomised controlled trial involving 110 bladder cancer patients screened positive for at least 1 SNAP factor and undergoing neoadjuvant chemotherapy before radical cystectomy. Patients allocated to the intervention group will receive five counselling sessions in 6 weeks including an integrated prehabilitation program covering the time period until surgery tailored to meet the individual patient's need for risk reduction. Patients are ensured that they are free to access support to lifestyle changes in the community.

Tracking Information

NCT #
NCT04088968
Collaborators
  • Aarhus University Hospital
  • Copenhagen University Hospital at Herlev
  • Rigshospitalet, Denmark
Investigators
Not Provided