Actively Recruiting

Age: 18Years +
FEMALE
NCT06590506

High Definition Medicine for Solid Tumors Oncology

Led by Centro Nacional de Investigaciones Oncologicas CARLOS III · Updated on 2024-09-19

300

Participants Needed

9

Research Sites

252 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The present study aims to analyze different genetic, phenotypic, environmental, social and lifestyle characteristics of cancer patients who are going to start a first line of cancer treatment with palliative intent and their possible relationship with tumor response or tolerance to treatment. In this way, the aim is to identify a series of variables that allow a better selection of patients and oncological treatments.

CONDITIONS

Official Title

High Definition Medicine for Solid Tumors Oncology

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of solid tumor cancer, starting first-line treatment for metastatic disease
  • Advanced tumor stage III or IV, not eligible for curative treatment
  • Preference for women with hormone-positive, HER2-negative breast cancer receiving CDK4/6 inhibitor plus hormone therapy
  • Women with lung or colon cancer of any subtype starting first-line treatment
  • Patients starting known treatments within clinical trials (excluding double-blind studies)
  • ECOG performance status less than 2
  • Ability to carry and use the wearable device
  • Access to a mobile device with internet and email
  • Ability to complete quality of life, nutrition, and mental health questionnaires
  • Provided written informed consent before screening
  • Patients with co-morbidities included
  • Pregnant women included
Not Eligible

You will not qualify if you...

  • Previously received cancer treatment for metastatic disease or with palliative intent
  • Planned participation in double-blind treatment trials
  • Other active malignant diseases that could affect study compliance or results, except treated basal cell carcinoma or cervical cancer in situ
  • Concurrent illnesses that significantly interfere with participation, as judged by the investigator
  • Use of implanted therapeutic electronic devices like pacemakers, defibrillators, or cardiac resynchronizers

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 9 locations

1

Hospital Universitario A Coruña

A Coruña, A Coruña/ Galicia, Spain, 15006

Actively Recruiting

2

Hospital Universitario de Fuenlabrada

Fuenlabrada, Madrid, Spain, 28942

Actively Recruiting

3

Hospital Son Espases

Palma de Mallorca, Mallorca / Baleares, Spain, 07120

Actively Recruiting

4

Complejo Hospitalario de Navarra

Pamplona, Navarre, Spain, 31008

Actively Recruiting

5

Hospital Virgen de la Macarena

Seville, Sevilla/ Andalucia, Spain, 41009

Actively Recruiting

6

ICO Hospitalet Bellvitge

Barcelona, Spain, 08908

Actively Recruiting

7

Hospital San Pedro Alcántara de Cáceres

Cáceres, Spain, 10003

Actively Recruiting

8

Hospital de La Princesa

Madrid, Spain, 28006

Actively Recruiting

9

Hospital General de Valencia

Valencia, Spain, 46014

Actively Recruiting

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Research Team

M

Miguel A Quintela, PhD

CONTACT

B

Berta Nasarre, Pharmacist

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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