Clinical trial · Interventional
PREoPerAtive pREhabilitation in Patients With Head and Neck Cancer or Liver Cancer (PREPARE)
NCT05745558CI-TRIAL-00066302PREPAREunknownN/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)
The objective of this study is to determine the feasibility (main aim) and effectiveness (secondary aim) of a prehabilitation program in patients with head and neck cancer or liver cancer. Participating patients will participate in a 3-to-6 week rehabilitation program consisting of training and nutritional, smoking cessation and psychosocial counselling.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer Head Neck | — | UNRESOLVED | — |
| Cancer Liver | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Prehabilitation | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Prehabilitation
- description
- A 3-to-6-week prehabilitation program consisting of training and nutritional, smoking cessation and psychosocial counselling.
- interventionNames
- Behavioral: Prehabilitation
Primary outcomes (3)
- measure
- Program satisfaction
- timeFrame
- At completion of the prehabilitation program (3-6 weeks after baseline)
- description
- Self-designed questionnaire score (score between 1-10, higher score means higher satisfaction)
- measure
- Program compliance
- timeFrame
- At completion of the prehabilitation program (3-6 weeks after baseline)
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Age ≥18 years * Diagnosis of head and neck cancer or liver cancer * Scheduled for surgery in Erasmus MC * Provision of written informed consent * Only patient with a waiting time of at least 3 weeks till surgery can participate in this study Exclusion Criteria: * Patients that do not understand the Dutch language * Patients with severe physical or psychological comorbidities that limit participation in the prehabilitation program
References
Publications (0)
Data not yet available
No reference posted for this study.