Actively Recruiting
Feasibility of a Preoperative, Multimodal Lifestyle Intervention in Patients With Breastcancer
Led by Maastricht University Medical Center · Updated on 2025-02-20
11
Participants Needed
1
Research Sites
74 weeks
Total Duration
On this page
Sponsors
M
Maastricht University Medical Center
Lead Sponsor
N
Nationaal Fonds tegen Kanker
Collaborating Sponsor
AI-Summary
What this Trial Is About
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, dropout, safety and acceptance. The secondary objective is to provide a preliminary evaluation of participant responses to a preoperative multimodal lifestyle intervention, on cardiorespiratory fitness, muscle strength, nutritional status, and fatigue in patients with breast cancer receiving neoadjuvant chemotherapy.
CONDITIONS
Official Title
Feasibility of a Preoperative, Multimodal Lifestyle Intervention in Patients With Breastcancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients diagnosed with stage I-III breast cancer eligible for neoadjuvant intravenous chemotherapy at the MUMC+
- Aged 18 years or older
- Eastern Cooperative Oncology Group (ECOG) Performance Status Scale grade 0-1
- Sufficient understanding of the Dutch language
You will not qualify if you...
- Tumor that is Human Epidermal growth factor Receptor 2 (HER2) positive
- Use of scalp cooling during chemotherapy
- Conditions that severely limit the ability to perform physical exercise
- Patients considered incapacitated by their attending medical specialist
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Maastricht University Medical Center
Maastricht, Limburg, Netherlands, 6229HX
Actively Recruiting
Research Team
H
Hanneke van Dijk - Huisman, PhD
CONTACT
A
Anouk Weemaes, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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