Feasibility of a Preoperative, Multimodal Lifestyle Intervention in Patients With Breastcancer
Recruiting
N/A
Interventional Study
Breast Cancer
Breast Neoplasms
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 11 (estimated)
- Sponsor
- Maastricht University Medical Center · Other
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About This Trial
The primary objective of this study is to investigate the feasibility of a multimodal prehabilitation programme consisting of MIET during neoadjuvant intravenous chemotherapy infusion, HITT and strength training during the last six weeks prior to surgery, and optimising nutritional intake throughout the total preoperative period in patients with breast cancer with respect to recruitment, adherence…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients diagnosed with stage I-III breast cancer eligible for neoadjuvant intravenous chemotherapy at the MUMC+
* Aged ≥18 years
* Eastern Cooperative Oncology Group (ECOG) Performance Status Scale grade 0-1 (Table 1)
* Enough understanding of the Dutch language
Exclusion Cr…
Contacts