Active, not recruitingNot applicableEN originalBreast cancerMetastatic / advanced

Promoting Active Living Among People With Metastatic Breast Cancer

⚠️

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

This trial is no longer recruiting — here are similar active trials

Matched by cancer type/biomarker, currently recruiting.

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The goal of this randomized, double-blind, multi-regional phase 3 study of cadonilimab combined with chemotherapy versus chemotherapy in combination with or without nivolumab for the first-line treatment of participants with HER2-negative, previously untreated, unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma trial is to compare OS between cadonilimab combined with chemotherapy and chemotherapy in combination with or without nivolumab in the ITT population.

RecruitingUnknown phase🇵🇱 PolandColorectal cancerMetastatic / advanced

Metastatic colorectal cancer or mCRC is a cancer that starts in the parts of the large intestine (the colon or rectum) and has already spread to other parts of the body. This cancer can be hard to treat because it can behave differently from one person to another. Over time, treatments may stop working, and side effects can build up. In later treatment stages, there are only a few standard medicine options available. Because of this, studies often look at both how long people live and how treatment affects quality of life. The main aim of this study is to see how long adults in Poland with mCRC live without their cancer getting worse (progression-free survival or PFS) when they receive fruquintinib after at least two previous treatments. Fruquintinib (TAK 113) is a medicine taken by mouth that is designed to slow tumor growth. Other aim is to find out how long adults in Poland with mCRC live while being treated with fruquintinib (overall survival or OS). The study also wants to record how fruquintinib is used in routine care in adults with mCRC in Poland (for example when treatment starts, changes in doses, and how long treatment continues). Another aim is to learn about people with mCRC, such as their medical history and past treatment as well as their quality of life while they are in the study. The study will look at data already existing in the participants' medical charts.

The goal of this clinical trial is to determine the most effective dose of EIK1005 that a person can take safely. Additionally, this study will test how well EIK1005 is tolerated alone and in combination with pembrolizumab in treating patients with advanced cancer.

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About the trial

Individuals with metastatic breast cancer are living longer but often face persistent fatigue, functional decline, and psychological distress. Physical activity is generally safe for this population and may alleviate symptom burden. Yet, limited interventions are tailored to the unique and needs and preferences of this population. This study aims to evaluate the acceptability and feasibility of a mindfulness- and acceptance-based physical activity program designed to support mental, social, and spiritual well-being among people with metastatic breast cancer. A single group, pretest-posttest trial (N=38) will be conducted to inform scalable strategies to promote active living and enhance quality of life among people with advanced cancer.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Postawiona diagnoza zaawansowanego raka piersi
  • •Zgoda lekarza na udział w badaniu
  • •Oczekiwana długość życia co najmniej 6 miesięcy
  • •Dobry stan ogólny (zdolność do wykonywania codziennych czynności)
  • •Umiejętność obsługi smartfona i interfejsu internetowego, ewentualnie z pomocą
  • •Wystarczająca wzrok i słuch do używania smartfona
  • •Wystarczająca sprawność rąk do używania smartfona
  • •Gotowość do pobrania i używania aplikacji badawczych

✗ Disqualifies

  • •Przeciwwskazania do aktywności fizycznej (jak niekontrolowane wysokie ciśnienie lub choroby serca)
  • •Nieustabilizowane przerzuty do kości
  • •Niepowstające przerzuty do mózgu
  • •Historia zaburzeń pamięci lub poważnych problemów neurologicznych
  • •Depresja ciężka zdiagnozowana w ostatnich 6 miesięcy
  • •Poważne zaburzenia psychiatryczne (zaburzenie afektywne dwubiegunowe, psychoza, schizofrenia)
  • •Aktualnie hospitalizowany
  • •Umieszczony w hospicjum

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Maximum age
99 Years
Last updated (source)
September 11, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (1)

TSET Health Promotion Research Center

Oklahoma City, United States

Share this trial

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

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