Emotional Distress in Patients With Metastatic Breast Cancer in First Line of Therapy

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

Few data about the impact of emotional distress (ED) on treatment efficacy in patients with metastatic breast cancer (mBC) are available. Aim of this study is to assess the outcomes of patients with mBC receiving first-line treatment according to the presence of baseline ED.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • Osoby powyżej 18. roku życia.
  • Potwierdzony rak piersi.
  • Brak wcześniejszego leczenia z powodu zaawansowanego raka piersi.
  • Leczenie zgodne ze standardami dla danego typu raka piersi (np. leki w połączeniu z chemioterapią lub terapie celowane).
  • Widoczne zmiany chorobowe na badaniach obrazowych.
  • Zgoda na udział w badaniu.

✗ Disqualifies

  • Poważne problemy ze zdrowiem psychicznym, które utrudniają zrozumienie zasad badania.
  • Niezdolność do wypełniania ankiet.
  • Inny nowotwór wykryty w ciągu ostatnich 3 lat.
  • Aktywne przerzuty do mózgu.
  • Przyjmowanie leków przeciwdepresyjnych lub przeciwlękowych.

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
June 17, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (37)

Ospedali Riuniti di Ancona

Ancona, Italy

CRO (Centro di Riferimento Oncologico)

Aviano, Italy

Azienda Usl Toscana centro - Ospedale Santa Maria Annunziata

Bagno a Ripoli, Italy

IRCCS Istituto Tumori Giovanni Paolo II

Bari, Italy

ASST Papa Giovanni XXIII

Bergamo, Italy

ASST Spedali Civili

Brescia, Italy

Ospedale A. Perrino

Brindisi, Italy

ASST della Valle Olona

Busto Arsizio, Italy

Ospedale Valduce

Como, Italy

Ospedale Careggi

Florence, Italy

Ospedale Policlinico San Martino

Genova, Italy

AOU Gaetano Martino di Messina

Messina, Italy

European Institute of Oncology

Milan, Italy

ASST Fatebenefratelli Sacco

Milan, Italy

Fondazione IRCCS Istituto Nazionale dei Tumori

Milan, Italy

IRCCS Ospedale San Raffaele

Milan, Italy

Ospedale Niguarda

Milan, Italy

Ospedale San Giuseppe MultiMedica

Milan, Italy

Policlinico di Milano

Milan, Italy

Azienda Ospedaliero-Universitaria di Modena

Modena, Italy

Azienda Ospedaliera Universitaria Federico II

Naples, Italy

Istituto Nazionale Tumori IRCCS Fondazione G. Pascale

Naples, Italy

Ospedale Maggiore di Novara

Novara, Italy

Policlinico Universitario Paolo Giaccone

Palermo, Italy

Policlinico San Matteo

Pavia, Italy

Azienda Ospedaliero Universitaria Pisana

Pisa, Italy

Azienda Ospedaliero Universitaria Pisana

Pisa, Italy

Azienda Usl Toscana centro - Ospedale di Prato Santo Stefano

Prato, Italy

Ospedale Infermi

Rimini, Italy

Policlinico Universitario Campus Bio-Medico

Roma, Italy

Policlinico Umberto I

Rome, Italy

Policlinico Universitario Agostino Gemelli IRCCS

Rome, Italy

Azienda Ospedaliero Universitaria di Sassari

Sassari, Italy

ASL CN2 - Ospedale Michele e Pietro Ferrero

Verduno, Italy

Azienda Ospedaliera Universitaria Integrata Verona

Verona, Italy

Ospedale Sacro Cuore Don Calabria - Negrar

Verona, Italy

ASST Brianza

Vimercate, Italy

Trial contact

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.

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