Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
FEMALE
NCT05656716

Multimodal Project

Led by Universidad de Granada · Updated on 2024-05-09

80

Participants Needed

1

Research Sites

85 weeks

Total Duration

On this page

Sponsors

U

Universidad de Granada

Lead Sponsor

U

University Hospital Virgen de las Nieves

Collaborating Sponsor

AI-Summary

What this Trial Is About

The main aim of this study is to determine the effect of a multimodal intervention (Nutrition and Exercise) on quality of life, emotional well-being, and secondary symptomatology in patients diagnosed with breast cancer during neoadjuvant chemotherapy treatment, and to compare them with the control group.

CONDITIONS

Official Title

Multimodal Project

Who Can Participate

Age: 18Years - 75Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with breast cancer who will undergo neoadjuvant treatment in the Oncology Unit of the Virgen de las Nieves University Hospital of Granada
  • Aged between 18 and 75 years
  • Willing to give consent and complete the entire intervention and follow-up appointments
  • Capable and willing to provide consent and understand study instructions and protocols
Not Eligible

You will not qualify if you...

  • Unable or unwilling to follow diet and exercise guidelines or having physical or psychological conditions that contraindicate inclusion
  • Failure to register required follow-up data
  • Any condition that impairs participation or poses personal risk, as judged by the investigator
  • Deemed unsuitable by the investigator for any other reason preventing data collection

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Granada

Granada, Spain

Actively Recruiting

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Research Team

L

Lucas Jurado-Fasoli

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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